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  • Cell & Developmental Biology  (2,672)
  • 1980-1984  (2,672)
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  • 101
    ISSN: 0148-7280
    Keywords: mouse ; embryo ; in vitro fertilization ; culture ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Techniques for culturing preimplantation mouse embryos from the two-cell stage to blastocyst are described, and the importance of this system to quality control assay the media and supplements used in human in vitro fertilization (IVF) procedures is discussed. Embryos from B6CBAF1 mice were cultured in a commonly used mouse culture medium, modified Krebs-Ringer-bicarbonate (Krebs'), or in a commonly used human culture medium, Ham's F10 nutrient mixture supplemented with human fetal cord serum (FCS), and results were not significantly different. Using the mouse embryo culture system, tests on 174 preparations of FCS resulted in 24.1% producing less than 75% morula or blastocyst stages after 72 h in culture, compared to 9.5% of the Krebs' control cultures. Results of the mouse embryo culture system using 98 FCS subsequently used in human IVF were compared to results from the VIP Human In Vitro Program of Eastern Virginia Medical School of Norfolk, Virginia, from June 1982 through June 1983. The data suggest that prescreening of media and supplements using this mouse embryo culture system may indicate sources of factors potentially detrimental to the success of human IVF procedures.
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  • 102
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 9 (1984), S. 175-181 
    ISSN: 0148-7280
    Keywords: human ; in vitro fertilization ; cleavage ; delayed insemination ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Two normal, healthy children have been born after an oocyte was collected from each of two patients during their natural menstrual cycle, incubated for many hours and then fertilized in vitro. Details of the follicular phase prior to oocyte recovery, fertilization and embryonic development in vitro, and replacement of the embryos are described in detail. One embryo cleaved rapidly after its delayed fertilization, with blastomeres of uneven size and cellular fragments. The luteal phase seemed to be weak in both patients.
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  • 103
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 9 (1984), S. 451-467 
    ISSN: 0148-7280
    Keywords: karyotype ; parthenote ; meiosis ; mitochondria ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Karyotypic and light and electron microscopical analyses were made of spontaneous preimplantation mouse parthenotes from the LT/Sv inbred strain. It was found that the activated oocyte and developing embryos were diploid. We believe that diploidization is achieved by the oogonium undergoing a premeiotic mitosis without cytokinesis followed by two meiotic divisions, thus producing diploid parthenotes.The developmental events with respect to membrane specialization, such as junctional complexes, were similar to those observed in fertilized embryos.A unique feature of the developing parthenote was the failure of the mitochondria to change during the morula stage. The mitochondria retained a few irregularly oriented cristae rather than many transversely oriented ones observed in morulae developing from fertilized eggs. The significance of this observation is discussed.
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  • 104
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Gamete Research 10 (1984), S. 91-91 
    ISSN: 0148-7280
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
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  • 105
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Gamete Research 10 (1984), S. 83-89 
    ISSN: 0148-7280
    Keywords: fowl sperm ; motility ; ATP ; potassium ; fertilizing ability ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Fowl semen when diluted in a glutamate-based medium without glucose, gradually lost its fertilizing ability during 4 hr of anaerobic incubation at 30°C. This incubation regime offered a system by which various in-vitro tests of spermatozoal viability could be assessed for their usefulness as monitors of fertilizing ability. Widely used tests such as spermatozoal enzyme leakage, dye exclusion, and morphology as assessed by light microscopy showed no change in spermatozoal status as the fertilizing ability declined. However the ability of sperm, during a short aerobic incubation to restore their motility and ATP and K+ concentrations, declined as did their fertilizing ability. When glucose was added to this re-aeration medium, spermatozoal motility, K+ and ATP concentrations, and fertilizing ability were restored to optimal levels. Thus the fertilizing ability of fowl sperm, following anaerobic storage at 30°C, appeared to be related to their ability to restore ATP and K+ concentrations and motility. An initial event in the loss of fertilizing ability was a loss in the ability of sperm to oxidise endogenous substrates. This could be restored by the addition of glucose.
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  • 106
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 10 (1984) 
    ISSN: 0148-7280
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
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  • 107
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 10 (1984), S. 233-239 
    ISSN: 0148-7280
    Keywords: chromosome ; spermatozoa ; sperm ; egg ; zona-free ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: An improved method for human sperm chromosome preparation is described. Improvements include (1) the use of a sperm population with high motility and normal morphology for insemination, (2) the insemination and postinsemination culture of zona-free eggs in Holmes medium, which does not require serum supplementation, (3) control of sperm concentration at insemination to avoid heavy polyspermy, (4) reduction of the occurrence of egg agglutination by placing the medium for postinsemination culture in a ring or crescent shape instead of a droplet, and (5) application of a two-step fixation method to augment the efficiency of chromosome preparation.
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  • 108
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 10 (1984), S. 319-325 
    ISSN: 0148-7280
    Keywords: immotile spermatozoa ; ultrastructural tail defects ; hamster ova penetration ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: We studied six men whose spermatozoa were immotile and possessed a variety of sperm tail structural abnormalities by electron microscopy. The semen of all six subjects had a normal percentage of oval forms and sperm undergoing capacitation and acrosome reaction. Despite the absence of motility, when incubated sperm from these subjects was added to a microdrop of medium containing zona pellucida-free hamster ova, sperm penetration or entry into the cytoplasm of from 1-9% of the eggs was evident with phase contrast microscopy. This latter finding suggests that, at least in this system, oocytes actively facilitate sperm incorporation. Penetration was absent when sperm of fertile men were rendered immotile, though still viable, by heat treatment.
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  • 109
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Gamete Research 10 (1984), S. 327-337 
    ISSN: 0148-7280
    Keywords: acrosin inhibitors ; acrosome ; evolution ; spermatogenesis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The acrosome of the mammalian spermatozoon contains proacrosin that is autocatalytically activated to become the proteolytic enzyme acrosin during the process of fertilization. Tschesche et al [1982] isolated specific acrosin inhibitors and suggested that they block prematurely activated acrosin. Antibodies against acrosin inhibitors purified from boar spermatozoa were used to demonstrate the evolutionaary relationship and the developmental pattern of the inhibitors in mammals. Using immunofluorescent techniques the following results were obtained: (1) The spermatozoa of man, boar, bull, ram, rat, rabbit, beaver, and mole stained positive in the acrosomal portion. (2) The round-headed spermatozoa of patients with globozoospermia and those in the ejaculates of fertile men lacked immunostaining for the inhibitors. (3) During spermatogenesis in all species, immunofluorescence for the acrosin inhibitors was first demonstrable in haploid spermatids and increased thereafter during spermatid differentiation. The stained area was found adjacent to the nuclear membrane, the position of the acrosome. (4) During teratogenesis of round-headed spermatozoa, the immunofluorescent staining for the inhibitors becomes separated from the nuclear membrane of the spermatids and is lost in late spermatids. Since identical results have been described for acrosin and acrosomal membrane proteins both in spermatozoa and spermatids of mammalian species and during spermiogenesis of patients with globozoospermia, our results are consistent with the localisation of the inhibitors in the acrosome. Immunostaining of spermatozoa of species belonging to five different mammalian orders with the antibody against boar acrosin-inhibitors is indicative of an evolutionary conservation of the inhibitors and their underlying genes.
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  • 110
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The fine structure of the kidney and the bladder of the bullfrog (Rana catesbeiana), the bullfrog tadpole, and the mudpuppy (Necturus maculosus) were studied with special attention to the innervation of renal tubule cells and bladder epithelial cells. In the bullfrog kidney, nerve terminals and varicosities were frequently associated with the tubule cells, apparently in an increasing order from the proximal tubule to the connecting tubule. Although these terminals and varicosities did not directly contact the tubular cell membrane, an aggregation of synaptic vesicles on the side facing the tubule was considered as morphological evidence that neurotransmitter can be released here and can affect the transport activity of the tubule cells. The association of nerve varicosities with canaliculi cells in the connecting tubule was also demonstrated. In the bullfrog tadpoles, renal tubule cells were occasionally innervated. In the mudpuppy, renal tubule cells were only poorly innervated. The epithelium of the bullfrog bladder was commonly innervated. Nerve terminals with synaptic vesicles were located very near basal cells and even contacted them directly on rare occasions. In the mudpuppy, the innervation of the bladder epithelium was observed infrequently. The bullfrog tadpoles did not possess an apparent bladder. In all materials studied, renal arterioles and bladder smooth muscle cells were innervated.
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  • 111
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Journal of Morphology 181 (1984), S. 155-160 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The architectural and histochemical properties of the anatomically distinct compartments of the semitendinosus muscle (ST) of mice, rats, guinea pigs, and rabbits show that the ST is composed of two separate compartments aligned in series - a destal compartment (STd) and a proximal one (STp). The STp is further subdivided into a ventral head (STpv) and a dorsal head (STpd). The muscle fibers were arranged in parallel to the line of muscle pull within each compartment. The STd has the longest and the STpv the shortest fibers in all species. The physiological cross-sectional area and the estimated tetanic tension was greatest in the STd. Based on the staining pattern for myosin ATPase (alkaline preincubation) and an oxidative indicator (NADH or SDH), the STpv has the highest percentage of slow-oxidative (SO) or SO plus fast-oxidative-glycolytic (FOG) fibers of any portion of the muscle. The differences in fiber-type distributions and architectural designs of the separate compartments suggest a specialization of function of the individual compartments.
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  • 112
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    New York, NY : Wiley-Blackwell
    Journal of Morphology 181 (1984), S. 205-220 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Light and electron microscopic techniques show that the eye of the marine prosobranch gastropod, Ilyanassa obsoleta, is composed of an optic cavity, lens, cornea, retina, and neuropile, and is surrounded by a connective tissue capsule. The adult retina is a columnar epithelium containing three morphologically distinct cell types: photoreceptor, pigmented, and ciliated cells. The retina is continuous anteriorly with a cuboidal corneal epithelium. The neuropile, located immediately behind the retina, is composed of photoreceptor cell axons, accessory neurons, and their neurites. The embryonic eye is formed from surface ectoderm, which sinks inward as a pigmented cellular mass. At this time, the eye primordium already contains presumptive photoreceptor cells, pigmented retinal cells, and corneal cells. Several days later, just before hatching, the embryonic eye remains in intimate contact with the cerebral ganglion. It has no ciliated retinal cells, neuropile, optic nerve, or connective tissue capsule and its photoreceptor cells lack the electron-lucent vesicles and multivesicular bodies of adult photoreceptor cells. As the eye and the cerebral ganglion grow apart, the optic nerve, neuropile, and connective tissue capsule develop.
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  • 113
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    New York, NY : Wiley-Blackwell
    Journal of Morphology 181 (1984) 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 114
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Journal of Morphology 181 (1984), S. 221-238 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The osteology of the head skeleton of marine catfish Arius tenuispinis is described in detail. The skeletal elements of the different regions are dealt with categorically. Bones of the ethmoidal, orbitotemporal, auditory, and occipital regions of the cranium; and the upper jaw, lower jaw, hyoid arch, hypobranchial, and opercular series of the visceral skeleton are described in detail. Identity of the ectopterygoid, mesopterygoid, and metapterygoid is established in accordance with the current nomenclature and accepted homologies. The shelving bone of the epiotic is found to be large, having articulation with the parapophyses of the complex vertebra. The head skeleton of A. tenuispinis conforms to the normal siluroid pattern.
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  • 115
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    Journal of Morphology 181 (1984), S. 239-270 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The mastoid auditory bulla of the extinct marsupial sabertooth, Thylacosmilus, has an enlarged, complex hypotympanic sinus but lacks an alisphenoid contribution. These are marked departures from the usual marsupial condition. Details of the ear region of Thylacosmilus are compared with those of the convergent, extinct placental sabertooth, Smilodon, and each is compared with less specialized related forms to define differences and similarities of the evolutionary paths that led to the striking overall convergence.Functional factors such as pressure transformer ratio (PTR), impedance transformer ratio (ITR), acoustic impedence at the eardrum, and the fraction of the sound energy theoretically transmitted to the inner ear cannot be estimated for Thylacosmilus because certain critical measures are still unknown (tympanum size, ossicle lever arm ratios). However, in both sabertooths enlarged complex hypotympanic sinuses, characterized by expansions and contractions, are greatly developed. They vastly increase middle ear space (volume) and must have influenced these factors. In both, the sinuses provide the large air volume needed to prevent excessive damping of sound energy transmission (Hunt and Korth, '80), and both are believed to have achieved a further modulation of the system from the cushioning or “pillow” effect of the confined air as it directly damps the tympanum itself. Thylacosmilus has still another feature that may have given greater control over damping of sound energy transmission: the direct opening (probably membrane covered) of one of the sinus cavities into the side of the meatal tube. In this feature, as in others noted earlier (Turnbull, '76, '78), we see a greater degree of specialization in this marsupial sabertooth than in a placental counterpart.
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  • 116
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    Journal of Morphology 181 (1984), S. 271-295 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: This report details certain morphological aspects of the feeding system of the lizard Trachydosaurus rugosus, an opportunistic omnivore, as a first step toward a functional characterization of its masticatory system. The skull is relatively solid and internally well braced; its anterodorsal elements are tightly tied to the integument and covering osteoderms. There is potential for intracranial kinesis and streptostyly. At small gapes, mandibular movements seem to be restricted to relatively simple, hingelike actions by a series of mechanical stops. The dentition features a progression of smaller to larger teeth posteriorly along the tooth row. The jaw adductor musculature is massive; other jaw muscles are relatively simple. The external adductor mass is particularly noteworthy in that it is subdivided into four mechanical units by a complex internal tendon tract (the coronoid aponeurosis). The internal adductor is composed of two separate gross muscles, pseudotemporalis (PST) and pterygoideus (PT). Each of these is subdivided into two main units by aponeurotic sheets, the PST by parts of the coronoid aponeurosis and the PT by a separate series. The form of the aponeurotic system in Trachydosaurus confounds the separation and identification of the adductor muscles and their component parts along the lines of traditional nomenclature, and underscores the need for separating criteria based on homology from those reflecting morphological and possibly functional divisions.
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  • 117
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    Journal of Morphology 181 (1984), S. 297-303 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Whenever individuals of the freshwater sponge Ephydatia fluviatilis belonging to different strains come into contact, they reject each other by building a nonmerging front. The present work describes the development, the structure, and the nature of the barrier secreted between two individuals. The observations reported give unequivocal data about the collagen nature of the incompatibility barrier. First, ultrastructural investigations reveal the presence of fibrils and microfibrils which are, respectively, typical of collagen and spongin. Second, incorporation of tritiated proline, a characteristic precursor of collagen and related products, is particularly intense in the front. The involvement of several cell types in the barrier formation is discussed. The allogeneic incompatibility reaction between E. fluviatilis individuals appears very close to the process of allograft chronic rejection that we formerly described for some marine sponges. Both phenomena are basically analogous to the process which fixes to and isolates the sponges from their substrate.
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  • 118
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Light and electron microscopy were used to examine the morphology of the mucosa of the diverticulum, anterior intestine, and transition zone in prefeeding and spontaneously feeding adult lampreys (Petromyzon marinus L.). Absorptive (either types A or B), ciliated, and enteroendocrine cells are present in all regions but the diverticulum and anterior intestine also possess zymogen (secretory) cells. Type A absorptive cells are restricted to the diverticulum and the rostral one-third of the anterior intestine and are characterized by abundant mitochondria and an extensive smooth tubular network. Type B absorptive cells, in the remainder of the anterior intestine and the transition zone, possess small numbers of these organelles but in the transition zone also have inclusion bodies. During feeding, abundant lipid droplets and lipoprotein (VLDL) accumulate in the cytoplasm of both types of absorptive cells and in the lateral intercellular and the perivascular spaces. Lipid is present to a limited extent in ciliated cells and is encountered only rarely in enteroendocrine and zymogen cells. Although the animals are obligate sanguivores, there is little evidence of iron within these mucosal cells. It is suggested that intestinal efficiency displayed by this animal is due in part to ion transport in osmoregulation in type A cells, lipid absorption in types A and B cells, and digestion through enzymes in zymogen cells.
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  • 119
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    Journal of Morphology 182 (1984), S. 63-69 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Renal tubules in the dog shark, leopard shark, and red skate were examined histologically and analyzed histochemically for enzymes. Cells of the distal and collecting tubules exhibit extensive interdigitations and large intercellular spaces, suggesting that these tubules are sites of sodium reabsorption. Although Na-K-ATPase is very scarce to nonexistent in the distal and collecting tubules, very intense carbonic anhydrase activity in these segments indicates that they secrete large amounts of hyrogen ion and reabsorb sodium by H+/Na+ exchange process. Epithelial cells of the necks are not interdigitated, tightly join adjacent cells, and have low enzyme activities. They seem to be passively permeable to the water. Necks are attached to the distal tubules with scant intervening stroma. It seems likely that the stroma has a high osmotic pressure resulting from absorption of solutes in the distal tubules. Water may be reabsorbed from necks to stroma because of a concentration gradient of the solutes distributed between these sites.
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  • 120
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    Journal of Morphology 182 (1984), S. 71-83 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Fourteen species of leiognathid fishes (Perciformes, Leiognathidae) from the Philippine Islands, Thailand, Japan, Indonesia, and Palau were examined for accessory secondary sexual dimorphism. Thirteen species exhibit either external dimorphism (a clear patch of skin on the flanks of males, a large clear patch of skin on the opercular margins of males, or a flank stripe in males) or internal dimorphism (large light organs in males) or both. Eight of the 14 species (and possibly as many as 11) exhibit both forms of sexual dimorphism. Two species show only internal light organ volume dimorphism, and one species shows neither external nor internal dimorphism. Sexual dimorphism is thus very common in leiognathids. The externally dimorphic skin patches are closely associated with the internally dimorphic light organ system in seven species (and possibly as many as ten), indicating a potential for light emission through the clear patches. A bioluminescent signaling function by males is therefore suggested for the sexual dimorphism in leiognathids, which may play an important role in the schooling behavior as well as in species and sexual recognition of these coastal fishes.
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  • 121
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: With the use of rabbit antisera against crustacean hyperglycemic hormone (CHH), it is possible to describe a distinct immunopositive reaction in a group of neurosecretory cells in the medulla terminalis ganglionic X-organ2 (MTGX2), in the MTGX-sinus gland tract, and in a considerable part of the sinus gland from several species of prawns belonging to the Palaemonidae. By introductory studies on the CHH system in Palaemon serratus, we can postulate a sequence in the activity cycle of the CHH-producing cells on the basis of differences in staining intensity of the immunoreaction and such morphometric parameters as cellular and nuclear diameter. By studying the CHH-producing system in combination with variations in the glucose level of the blood, an “inverse relationship” is observed between the number of immunoreactive cells and the blood glucose level during different periods of the year as well as during different stages of the molting cycle. A “shift in phase” of this correlation during the diurnal cycle suggests that several rhythmical phenomena may play a role in the regulation of glycemia in Crustacea.
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  • 122
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    Journal of Morphology 182 (1984) 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 123
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    Journal of Morphology 182 (1984), S. 115-123 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: A large mechanosensory campaniform sensillum (LCS) is found close to the flagellum/pedicellus joint in the antennae of the blowfly Calliphora erythrocephala. The LCS possesses a single sensory cell, enveloping cells and a cuticular stimulus-conducting structure. The distal part of the sensory process is developed as a tubular body and is connected to the two parts of the stimulusconducting apparatus. The sensory cell is characterized by the complete absence of ciliary structures in the transition zone between dendrite and sensory process.
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  • 124
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    Journal of Morphology 179 (1984), S. 263-271 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The anterior limb bud mesenchyme cells of stage 24 chick embryos were dissociated by trypsinization followed by gentle pipetting, and placed in a tissue culture medium of F12 containing 10% fetal calf serum and antibiotics. As the cells became nearly confluent, some of them were exposed to colchicine or vinblastine sulfate for durations as long as 48 hr. The control and antitubulin-treated cells were processed for transmission electron microscopy and the ultrastructure of the cells was compared. Annulate lamellae (AL) were observed in small amounts in both control and antitubulin-treated cells. The amount of AL did not markedly differ in the control versus antitubulin-treated cells. Furthermore, few multinucleated cells were observed in antitubulin-treated cultures. These results indicate that prolonged culture of cells in antitubulins need not, in itself, lead to a condition of enhanced AL development as reported in several other studies using various cell types.
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  • 125
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    Journal of Morphology 179 (1984), S. 229-242 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Wild-collected adults of Bombina orientalis are bright green dorsally and red to red-orange ventrally. As a prelude to an analysis of the differentiation of pigment cells in developing B. orientalis, we describe structural and chemical aspects of the fully differentiated pigment pattern of the “normal” adult.Structurally, differences between dorsal green and ventral red skin are summarized as follows: (1) Dorsal green skin contains a “typical” dermal chromatophore unit comprised of melanophores, iridophores, and xanthophores. Red skin contains predominantly carotenoid-containing xanthophores (erythrophores), and skin from black spot areas contains only melanophores. (2) In ventral red skin, there is also a thin layer of deep-lying iridophores that presumably are not involved in the observed color pattern. (3) Xanthophores of red and green skin are morphologically distinguishable from each other. Dorsal skin xanthophores contain both pterinosomes and carotenoid vesicles; ventral skin xanthophores contain only carotenoid vesicles. Carotenoid vesicles in dorsal xanthophores are much larger but less electron dense than comparable structures in ventral xanthophores.The presence of carotenes in ventral skin accounts for the bright red-orange color of the belly of this frog. Similar pigments are also present in green skin, but in smaller quantities and in conjunction with both colored (yellow) and colorless pteridines. From spectral data obtained for xanthophore pigments and structural data obtained from the size and arrangement of reflecting platelets in the iridophore layer, we attempt to explain the phenomenon of observed green color in B. orientalis.
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  • 126
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    Journal of Morphology 179 (1984), S. 243-262 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The fine structure of the male reproductive system of the hermaphroditic brittle-star, Amphipholis squamata, has been studied in specimens from both the Pacific coast (Washington) and the Atlantic coast (New Hampshire). Each testis is a small (100-μm) sphere and is attached to the internal wall of the bursa by peritoneal suspensor cells. Occasional flagellated cells are found on the external surface of the testis. The testicular wall of A. squamata is a multilayered structure, similar to that of other ophiuroids, but the hemal sinus is PAS negative in this species. Germinal cells are surrounded throughout their development by the filopodia of interstitial cells. Adjacent interstitial cells are interconnected, and thus form a structural network within the testis. Positionally and functionally, the interstitial cells resemble Sertoli cells; however, their origin, behavior and ultrastructure are different in many ways.Spermatogenesis includes a series of cyclical changes (aspermatogenic phase, proliferative phase, differentiative phase, and evacuative phase). Within a single testis, the resulting production of sperm is in short pulses, but if all 10 testes are taken together, sperm are produced continuously throughout the year. The events of spermiogenesis closely follow those that have been described in other echinoderms. However, we have provided new information on the release of excess cell membranes and the fusion process of mitochondria.The mature spermatozoa of A. squamata are flagellated and motile, and have “primitive” structural features, in spite of the fact that they fertilize the eggs inside the genital bursae. The spermatozoa do not, as was previously thought, enter the bursa by rupture of the adjacent walls. Instead, they are ejaculated through a gonoduct into the rapid incurrent flow of water entering the bursa. The locomotion of the spermatozoa is in eccentric spirals, due to the unusually large angle at which the flagellum is inserted into the base of the sperm.
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  • 127
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    Journal of Morphology 179 (1984), S. 273-289 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The larval nephridia of the brackish-water polychaete Nereis diversicolor are described for the first time, and have been studied to determine if their times of development and structural characteristics are consistent with a role in the osmotic regulation of the larva. As shown in serial paraffin sections and by interference-contrast optics, the nephridia of the three-setiger larva consist of a single pair of very large metanephridia, arising in the 3rd larval setiger, but with their elongated terminal ducts and coiled ciliated tubules pushed forward into the 2nd setiger; their open metanephrostomes and anterior anchoring filaments lie dorsal to the 2nd set of setae. In contrast, the definitive or juvenile metanephridia, arising in the 4th and subsequently formed setigerous segments, have short terminal ducts and coiled ciliated tubules confined to the segments on which their external nephropores open; their nephrostomes are ventrally located and open into the rear of the next anterior segment. These findings are in contrast to the claims of Edouard Meyer (1887), who described two pairs of closed protonephridia in the 2nd and 3rd larval setigers of Perinereis cultrifera. Although it is not excluded that the single larval pair of metanephridia of N. diversicolor may arise as protonephridia, Meyer's claim of two pairs of larval protonephridia was an observational error. The larval nephridia of the marine Platynereis dumerilii resemble in form, but are considerably smaller than, those of N. diversicolor. It is concluded that the hypertrophied pair of larval metanephridia of N. diversicolor is an evolutionary adaptation to existence in habitats of low and unpredictably varying salinity. Their development occurs irrespective of the prevailing salinity; hence, it must be genetically determined.
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  • 128
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    Journal of Morphology 180 (1984) 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 129
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    Journal of Morphology 179 (1984), S. 291-304 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The fine structure of α L929 fibroblasts cultured in colchicine or vinblastine sulfate for periods as long as 48 hr was compared to control cells not exposed to antitubulins. In response to prolonged antitubulin culture, several changes in cell ultrastructure were noted: (1) Control fibroblasts contain cytoplasmic annulate lamellae (AL), but (2) prolonged exposure to either vinblastine sulfate or colchicine results in enhanced development of AL. (3) Single pore complexes are present in the rough-surfaced endoplasmic reticulum (rER) in both control and antitubulin-treated cells, but stacked porous cytomembranes also occur under both conditions. (4) Polyribosomes often are closely associated or continuous with the pore complexes. (5) Many antitubulin-treated cells become multinucleate. Some nuclei in both control and antitubulin-treated cells contain large and multiple nucleoli. (6) The large and multiple nucleoli are either attached directly to the inner membrane of the nuclear envelope or to infoldings of the nuclear envelope. (7) Antitubulin-treated cells, after 48-hr exposure, appear also to contain enhanced quantities of smooth-surfaced endoplasmic reticulum (sER) and cytoplasmic filaments (and in some cells, lysosomes and rER as well) when compared to untreated cells. (8) In both control and colchicine-treated cells, AL can exhibit continuity with either rER or sER. Further, (9) all three membrane systems may at times be continuous, but the quantity of these membranes appears to be greater in colchicine-treated cells than in control cells. The results are discussed with respect to possible functional significance.
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  • 130
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    Journal of Morphology 179 (1984), S. 305-321 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The freeze-fracture technique has been used to obtain detailed information about cuticular constituents and outgrowths of the external skeleton of labella and antennae in the bluebottle fly Calliphora vicina and the antennae of the small moth (Yponomeuta spp.). The lamellated exoskeleton has a fibrous endocuticle and an exocuticle lacking fibers. Ductuli connecting the inside of the animal with the outside run perpendicularly through the endocutile and at angles of up to 45° in the exocuticle. Skeletal outgrowths lack fibers and display fracture features similar to those of the exocuticle. Among those having neuronal endings, gustatory, olfactory, and tactile hairs can be recognized. Noninnervated outgrowths can be subdivided into scales and pseudotrichia. Criteria such as shape, length/width-ratio of hairs, texture, presence and place of pores, shape of pores, and form of the socket or base are presented for further classification. Cuticular features of single-walled olfactory hairs of Calliphora are compared with those of several other species. Based on the shape of the pores, five types of hairs can be distinguished using literature data. It is concluded that the freeze-fracture technique is a valuable tool with which to describe the microarchitecture of the insect exoskeleton and supplements scanning electron microscopy, which is useful for describing the overall skeletal features.
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  • 131
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    Journal of Morphology 180 (1984), S. 145-157 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Light and electron microscopic techniques were used to study the cellular and ultrastructural components of the regenerating adult eye of the marine prosobranch gastropod Ilyanassa obsoleta. Behavioral tests were used to determine return of vision in animals with generated eyes. As early as 3 days after removal of the adult eye, the regenerating eye primordium appeared as a pigmented mass of cells that invaginated from the surface epithelium in the area of the wound. Twelve days after eye removal, the regenerating eye was very similar to the postmetamorphic juvenile eye and to the adult eye: It contained a retinal layer, as well as an extracellular lens, cornea, connective tissue capsule, and forming optic nerve; vision had returned. Growth of the eye and its components was linear; size ratios established among forming eye components were maintained during growth.The events of eye regeneration appear to recapitulate embryonic eye formation. The sequence of invagination, pigmentation, and lens, optic nerve, and retinal pattern formation are similar.
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  • 132
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    Journal of Morphology 180 (1984), S. 171-171 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: No Abstracts.
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  • 133
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    Journal of Morphology 180 (1984) 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 134
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    Journal of Morphology 180 (1984), S. 213-221 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The bursa compulatrix of the Monarch butterfly was investigated utilizing light microscopy, histochemistry, and scanning and transmission electron microscopy in order to relate its morphology to the release of sperm from the spermatophore. The bursa has a row of large chitinous teeth on either side of the organ. The dorsal and ventral surfaces are covered with chitinous plates, the plates having bristles on one side. A single layer of cells lies under both the plates and teeth, one columnar cell under each plate, one cuboidal cell under each tooth. The toothed area has no muscle cells. However, the dorsal and ventral hemispheres of the bursa each have a crescent-shaped packet of muscle fibers that traverse the organ; there are no longitudinal fibers. Spermatophores with thick walls were found in the bursal lumen. Morphological evidence suggests that the presence of the spermatophores is sensed by the bristles and that the packets are opened by contraction of the muscles bringing the large teeth into contact with the spermatophore wall.
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  • 135
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    Journal of Cellular Biochemistry 24 (1984), S. 307-317 
    ISSN: 0730-2312
    Keywords: secretory component ; bile ; IgA ; immunoblot ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Secretory component is a receptor for polymeric immunoglobulins on epithelial cells and hepatocytes that facilitates transport of polymeric immunoglobulins into external secretions. Little is known about the transcellular migration of secretory component-polymeric IgA complexes or the membrane forms of secretory component. We therefore examined rat bile and liver membranes to identify and compare the various molecular species of secretory component. Bile or liver membrane proteins were electrophoresed in sodium dodecyl sulfate-polyacrylamide gels and electrophoretically transferred to nitrocellulose membranes. Protein profiles on blots were probed with antisecretory, component antiserum, and the immunoreactive bands were visualized by indirect immunoperoxidase staining. Bile collected in the presence of proteolytic inhibitors showed an immunoreactive doublet band (Mr = 82,000 and 78,000) in the molecular weight range of free secretory component. By contrast, free secretory component in bile collected in the absence of proteolytic inhibitors and purified by affinity chromatography migrated as a single protein with an Mr = 70,000. Both components of the free secretory component doublet bound dimeric IgA when blots were probed with human dimeric IgA. Crude liver membranes prepared in the presence of proteolytic inhibitors showed two immunoreactive secretory component-containing bands, Mr = 107,000 and 99,000, whereas membranes prepared without proteolytic inhibitors showed two smaller immunoreactive bands; one of these proteolytically severed proteins comigrated with the 82,000-dalton free secretory component in bile. These results indicate that membrane forms of secretory component are present in rat liver. The observations that the membrane secretory component is larger than biliary free secretory component and yields biliary SC-like forms of secretory component upon proteolysis support the hypothesis that free secretory component in bile is a proteolytic product of larger liver membrane-associated secretory component.
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  • 136
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    Keywords: leucine binding protein ; protein secretion ; proteolysis ; degradation ; site-directed mutagenesis ; membrane potential ; processing ; periplasmic proteins ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The leucine-specific binding protein (LS-BP), a periplasmic component of the Escherichia coli high-affinity leucine transport system, is initially synthesized in a precursor form with a 23 amino acid N-terminal leader sequence that is removed during secretion of the protein into the periplasm. Using in vitro mutagenesis, deletion mutants of the LS-BP gene have been constructed with altered or missing amino acid sequences in the C-terminal portion of the protein. These altered binding proteins exhibited normal processing and secretion but were rapidly degraded in the periplasmic space. In the presence of an uncoupler of the transmembrane potential (CCCP) the precursor forms accumulated in the membrane and were protected from degradation. The altered binding proteins also were secreted by spheroplasts of E coli, after which they were easily detected.
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  • 137
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    Journal of Cellular Biochemistry 24 (1984), S. 345-356 
    ISSN: 0730-2312
    Keywords: bacterial protein secretion ; transmembrane potential ; secondary structure prediction ; protein folding ; electric field ; domain formation ; binding proteins ; periplasmic ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The synthesis and processing of the periplasmic components of the leucine transport system of E coli have been studied to determine the role played by transmembrane potential in protein secretion. Both the leucine-isoleucine-valine binding protein and the leucine-specific binding protein are synthesized as precursors with 23 amino acid N-terminal leader sequences. The processing of these precursors is sensitive to the transmembrane potential. Since the amino acid sequence and the crystal structure have been determined for the leucine-isoleucine-valine binding protein, it and the closely related leucine-specific binding protein represent convenient models in which to examine the mechanism of protein secretion in E coli. A model for secretion has been proposed, suggesting a role for transmembrane potential. In this model, the N-terminal amino acid sequence of the precursor is assumed to form a hairpin of two helices. The membrane potential may orient this structure to make it accessible to processing. In addition, the model suggests that a negatively charged, folded domain of the secretory protein may electrophorese toward the trans-positive side of the membrane, thus providing an additional role for the transmembrane potential.
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  • 138
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    Journal of Cellular Biochemistry 24 (1984), S. 373-384 
    ISSN: 0730-2312
    Keywords: dyneins ; calmodulin ; cilia ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Cilia from the protozoan Tetrahymena pyriformis were demembranated and then extracted for 5 min with a buffer containing 0.5 M NaCl. The briefly extracted axonemal pellet was then reextracted for about 20 hr. The soluble material obtained from each extraction was resolved into 14S and 30S dynein ATPases by sedimentation on sucrose density gradients and tested for sensitivity to added calmodulin. The 14S dynein obtained by a 5-min extraction was generally insensitive to added calmodulin, whereas that obtained by 20-hr extraction of the 5-min extracted axonemes was activated by calmodulin, the activation being much larger in the “light” 14S fractions than in the “heavy” fractions. The 30S dynein ATPase obtained by a 5-min extraction was generally activated over 1.6-fold by added calmodulin, whereas that obtained by the subsequent long extraction was usually activated only 1.3-fold. After further purification of the 5-min extracted 30S dynein and of the 5-min to 20-hr-extracted 14S dynein on DEAE-Sephacel, these dyneins retained much of their calmodulin activatability. The ATPase activity of both 14S and 30S dyneins was inhibited more strongly by erythro-9-[3-(2-hydroxynonyl)] adenine and by vanadate in the presence of added calmodulin than in its absence. These data suggest that the only ATPase activity present in the fractions studied is that of the dyneins and demonstrate that both the 14S and 30S dynein ATPases may be obtained in forms mat are activated by added calmodulin as well as in forms that are insensitive to added calmodulin.
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  • 139
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    Journal of Cellular Biochemistry 24 (1984), S. 385-393 
    ISSN: 0730-2312
    Keywords: human erythrocyte ; shape ; band 3 ; ATP ; membrane ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The ATP-dependent transformation of crenated white human erythrocyte ghosts into smoothed disc and cup forms is inhibited by the soluble 40-45-kilodalton (kDa) cytoplasmic portion of the major transmembrane protein, band 3. The band 3 fragment was prepared by chymotryptic treatment of inverted vesicles stripped of peripheral proteins. When present at ≥0.2 mg per mg membrane protein (ie, ≥2 mol fragment per mol endogenous band 3), the fragment significantly reduced the rate of shape change but did not alter the proportion of membranes that were ultimately converted into smoothed forms (〉90%). The inhibitory activity of the fragment could not be attributed to contamination of the fragment preparation by actin or proteolytic enzymes. ATP-independent shape transformation was not inhibited. The band 3 fragment may compete with endogenous, intact band 3 for an association with the spectrin-actin network required for ATP-dependent smoothing of crenated membranes.
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  • 140
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    Journal of Cellular Biochemistry 25 (1984) 
    ISSN: 0730-2312
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 141
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    Journal of Cellular Biochemistry 24 (1984), S. 395-403 
    ISSN: 0730-2312
    Keywords: lysine N6-hydroxylase ; Aerobacter aerogenes 62-1 ; hydroxamate ; siderophore ; glutamine stimulation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Glutamine may serve as an activator and/or regulator of the N6-hydroxylase (E.C. 1.14.99) of Aerobacter aerogenes 62-1. Activation and stabilization of N6-hydroxylase activity was observed both in vivo and in vitro. Growth in a glutamine-supplemented medium resulted in (1) maximum N6-hydroxylase activity at an earlier stage of growth and (2) higher N6-hydroxylase activity and continued aerobactin synthesis into stationary phase. Storage of P2 in the presence of L-glutamine (1 mM) significantly increased the lifetime of the labile N6-hydroxylase activity. Inclusion of L-glutamine in the incubation mixture typically resulted in a 2-3-fold activation of the hydroxylase activity. The stimulatory effect of glutamine was independent of and additive to the enhancement of N6-hydroxylation by the active component(s) in the supernatant, S2 fraction. Glutamic acid-γ-semihydrazide activated slightly in the absence of glutamine but activation of the system by glutamine was decreased by this compound. Azaserine was shown to be an uncompetitive inhibitor with respect to lysine and this inhibition was not reversed by glutamine.
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  • 142
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    Journal of Cellular Biochemistry 25 (1984), S. 197-212 
    ISSN: 0730-2312
    Keywords: calmodulin ; dynein ; ATPase ; anion ; solubilization ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The basal ATPase activity of 30S dynein, whether obtained by extraction of ciliary axonemes with a high (0.5 M NaCl) or low (1 mM Tris-0.1 mM EDTA) ionic strength buffer is increased by NaCl, NaNO3, and Na acetate, with NaNO3 causing the largest increase. The calmodulin-activated ATPase activity of 30S dynein is also increased by addition of NaCl, NaNO3, or Na acetate, but the effects are less pronounced than on basal activity, so that the calmodulin activation ratio (CAR) decreases to 1.0 as salt concentration increases to 0.2 M. These salts also reduce the CAR of 14S dynein ATPase to 1.0 but by strongly inhibiting the calmodulin-activated ATPase activity and only slightly inhibiting the basal activity. Sodium fluoride differs both quantitatively and qualitatively from the other three salts studied. It inhibits the ATPase activity of both 14S and 30S dyneins at concentrations below 5 mM and, by a stronger inhibition of the calmodulin-activated ATPase activities, reduces the CAR to 1.0. Na acetate does not inhibit axonemal ATPase, nor does it interfere with the drop in turbidity caused by ATP and extracts very little protein from the axonemes. NaCl and, especially, NaNO3, cause a slow decrease in A350 of an axonemal suspension and an inhibition of the turbidity response to ATP. NaF, at concentrations comparable to those that inhibit the ATPase activities of the solubilized dyneins, also inhibits axonemal ATPase activity and the turbidity response. Pretreatment of demembranated axonemes with a buffer containing 0.25 M sodium acetate for 5 min followed by extraction for 5 min with a buffer containing 0.5 M NaCl and resolution of the extracted dynein on a sucrose density gradient generally yields a 30S dynein that is activated by calmodulin in a heterogeneous manner, ie, the “light” 30S dynein ATPase fractions are more activated than the “heavy” 30S dynein fractions. These results demonstrate specific anion effects on the basal and calmodulin-activated dynein ATPase activities, on the extractability of proteins from the axoneme, and on the turbidity response of demembranated axonemes to ATP. They also provide a method that frequently yields 30S dynein fractions with ATPase activities that are activated over twofold by added calmodulin.
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  • 143
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    Journal of Cellular Biochemistry 26 (1984) 
    ISSN: 0730-2312
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 144
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    Journal of Cellular Biochemistry 25 (1984), S. 213-229 
    ISSN: 0730-2312
    Keywords: human and rat mammary tumour cells ; polypeptide growth factor ; peptide-isolation methods ; sheep pituatory gland ; estrogen-responsive cell growth ; prolactin ; growth hormone ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: A growth factor for rat and human mammary tumor cells (MTGF-Pit) was isolated from lyophilized powders of whole sheep pituitaries by a rapid four-step procedure utilizing acetic acid extraction, heating at 93°C, and sequential chromatography in 0.10 M acetic acid on sulphopropyl Sephadex and Sephadex G-50. From 10 g of pituitary powder, 8-10-mg amounts of MTGF-Pit were isolated. By 8 M urea, 0.1% SDS-12.5% polyacrylamide gel electrophoresis analysis followed by Coomassie blue staining, this preparation was shown to be one major stained band. When assayed for growth effects on cells maintained in serum-free medium, 5.1-19.2 nM MTGF-Pit half replaced the growth of MTW9/PL rat and MCF-7 and T-47D human mammary tumor cells in response to 2% to 10% serum. MTGF-Pit shows mitogenic activity toward normal human diploid fibroblasts only at concentrations in excess of 2.5 × 10-4 M, while rat fibroblasts are unresponsive even at this high concentration. From data available, we conclude that a mitogenic activity for epithelial-type mammary cells has been isolated, and this growth factor appears to be a previously undetected acid- and heat-stable activity that is highly abundant (estimated at 0.16% or more of the total dry weight of the pituitary powder). The isolated ovine MTGF-Pit (3,900 ± 200 daltons) does not share the molecular weight of native prolactin (24,000 daltons), “cleaved” prolactin (16,000 daltons), or growth hormone (22,000 daltons), and by all tests applied cannot be replaced with other known hormones and purified growth factors. We conclude a potent new mammary tumor cell mitogenic activity has been identified from sheep pituitaries.
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  • 145
    ISSN: 0730-2312
    Keywords: α1-proteinase inhibitor ; trypsin ; antithrombin III ; thrombin ; ligand endocytosis ; proteinase regulation ; hepatocyte uptake ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: In vivo clearance studies have indicated that the clearance of proteinase complexes of the homologous serine proteinase inhibitors α1-proteinase inhibitor and anti-thrombin III occurs via a specific and saturable pathway located on hepatocytes. In vitro hepatocyte-uptake studies with antithrombin III-proteinase complexes confirmed the hepatocyte uptake and degradation of these complexes, and demonstrated the formation of a disulfide interchange product between the ligand and a cellular protein. We now report the results of in vitro hepatocyte uptake studies with α1-proteinase inhibitor-trypsin complexes. Trypsin complexes of α1-proteinase inhibitor were prepared and purified to homogeneity. Uptake of these complexes by hepatocytes was time and concentration-dependent. Competition experiments with α1-proteinase inhibitor, α1-proteinase inhibitor-trypsin, and antithrombin III-thrombin indicated that the proteinase complexes of these two inhibitors arc recognized by the same uptake mechanism, whereas the native inhibitor is not. Uptake studies were performed at 37°C with 125I-α1-proteinase inhibitor-trypsin and analyzed by sodium dodecyl sulfate-gel electrophoresis in conjunction with autoradiography. These studies demonstrated time-dependent uptake and degradation of the ligand to low molecular weight peptides. In addition, there was a time-dependent accumulation of a high molecular weight complex of ligand and a cellular protein. This complex disappeared when gels were performed under reducing conditions. The sole cysteine residue in α1-proteinase inhibitor was reduced and alkylated with iodoacetamide. Trypsin complexes of the modified inhibitor were prepared and purified to homogeneity. Uptake and degradation studies demonstrated no differences in the results obtained with this modified complex as compared to unmodified α1-proteinase inhibitor-trypsin complex. In addition, the high molecular weight disulfide interchange product was still present on sodium dodecyl sulfate-polyacrylamide gel electrophoresis of solubilized cells. Clearance and clearance competition studies with approteinase inhibitor-trypsin, alkylated α1-proteinase inhibitor-trypsin, antithrombin III-thrombin, and antithrombin III-factor IXa further demonstrated the shared hepatocyte uptake mechanism for all these complexes.
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  • 146
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    Journal of Cellular Biochemistry 26 (1984), S. 35-45 
    ISSN: 0730-2312
    Keywords: desmosome ; immunological analysis ; immunoblotting ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: A panel of monoclonal antibodies and conventional antisera directed against desmosomal proteins from bovine muzzle epidermis was used Io identify immunologically related proteins from two other bovine stratified squamous epithelia, cornea and esophagus. Desmosome-enriched tissue fractions were prepared from epidermis, cornea, and esophagus. These tissue extracts were electrophoresed on sodium dodecyl sulfate (SDS)-polyacrylamide gels, blotted onto nitrocellulose paper, and labeled using an indirect immunoperoxidase technique. Labeling with the conventional antisera demonstrates that each of the previously characterized epidermal desmosomal proteins or protein families has an immunologically cross-reacting counterpart in cornea and esophagus. However, chemical differences between homologous desmosomal proteins in these three tissues have also been detected. The corresponding proteins in the different tissues have similar but not always identical apparent molecular weights. Moreover, tissue-restricted antigenic determinants were detected in two of the desmosomal protein families using four monoclonal antibodies, each of which recognizes a distinct antigenic determinant.
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  • 147
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    Journal of Cellular Biochemistry 26 (1984), S. 19-33 
    ISSN: 0730-2312
    Keywords: dynein ; cytoplasmic dynein ; ATPase ; sea urchin eggs ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: An improved method has been devised for the purification of cytoplasmic dynein from sea urchin eggs (Strongylocentrotus droebachiensis and S purpuratus). This protocol introduces three changes over a previously published procedure (Hisanaga and Sakai: J Biochem 93:87, 1983) - the substitution of diethylaminoethyl (DEAE)-cellulose for hydroxylapatite chromatography, the elimination of sucrose density gradient centrifugation, and the use of phosphoceliulose chromatography. These changes reduce the time and increase the efficiency of the purification procedure. The purified egg cytoplasmic dynein has enzymatic properties in common with axonemal dynein, including ionic specificity (Ca++ATPase/ Mg++ATPase = 0.8) and inhibition by sodium vanadate and erythro-9-2,3-hydroxynonyl adenine (EHNA). As assayed by silver staining of polyacrylamide gels, the cytoplasmic dynein is composed of two high molecular weight polypeptides ( 〉 300 kilodaltons) that comigrate with flagellar dynein heavy chains, and lesser amounts of three lower molecular weight bands. None of these polypeptides appears to contain bound carbohydrate. The purification procedure can be modified slightly to allow the preparation of cytoplasmic dynein in only 2 days from as little as 3-5 ml of packed eggs, a 20-fold reduction over the previous method. This more rapid and efficient method will facilitate the investigation of cytoplasmic dynein in other systems where starting material is limited, including tissue culture cells and nerve axoplasm.
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  • 148
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    Journal of Cellular Biochemistry 26 (1984) 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 149
    ISSN: 0730-2312
    Keywords: cellular growth ; protein synthesis ; protein turnover ; lysosomes ; proteolysis ; myeloma ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The fractional rates of protein synthesis (ks) and degradation (kp) were studied in the myeloma cell line SP2/0-AG14 grown at different rates (kg). Cells in spinner flask suspension cultures were maintained at constant cellular density for prolonged periods by replacement perfusion of labeling medium at a rate equivalent to the rate of growth. Total protein synthesis was calculated from the specific-radioactivity of labeled L-leucine in the precursor (medium) and cellular protein. Fractional synthesis rates determined by approach to equilibrium labeling were the same as those determined by equilibrium-pulse labeling kinetics and pulse-chase kinetics. The rate of protein degradation was determined from the established relationship kg = ks - kp. Protein synthesis rates remained constant over a threefold range in the rate of cell growth. At relatively slow growth rates (kg = 0.017/hr) turnover represented a major fraction of total synthesis (kp = 0.032/hr = 0.65ks). At rapid growth rates (kg = 0.058/hr) the value of kp was less than 0.005/hr. No major difference was observed between the ks determined for individual cellular proteins (separated by SDS-polyacrylamide (7.5%) gel electro-phoresis) from rapid- and slow-growing cultures. Thus, with an invariable ks, any change in growth rate is due to an inverse change in the rate of turnover. Since turnover is the balance between synthesis and degradation and since synthesis is unchanging then changes in the growth rate of SP2/0-AG14 should be due to changes in the rate of protein degradation. Experiments were therefore performed to determine the origin of the degradative machinery, ie, cytosolic or lysosomal; autolysis of prelabeled cellular protein (in vitro) was observed only at acidic pH (4.2) and WUS totally inhibited by addition of lcupcptin (10 μM) and pepstatin (2 μM), the specific inhibitors of lysosomal cathepsins B (L) and D, respectively. Since growth rate appears to be regulated by the alterations in the rate of protein degradation and degradation (in vitro) in SP2/0-AG14 appearsto be lysosomal, then one should be able to alter the rate of cellular growth by interfering with rate of lysosomal proteolysis. Indeed, when the lysosomotropic amine NH 4Cl (10 mM) is added to cells growing with a kg of 0.018/hr ± 0.001 (ks = 0.050/hr ± 0.002) the growth rate increased to 0.051/hr ± 0.002 without change in the rate of protein synthesis (ks = 0.049/hr ± 0.003). It is suggested from our data that the cellular growth rate of SP2/0-AG14 is regulated by the lysosomal apparatus; whether this regulation is itself regulated by either a specific compartmentalization of the lysosomal proteinases and/or their substrates or by endogenous protease inhibitors, should prove to be an exciting area for future investigation.
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  • 150
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    Journal of Cellular Biochemistry 26 (1984), S. 65-73 
    ISSN: 0730-2312
    Keywords: lyphokines ; interleukin 1 ; macrophage cell line ; protein complex ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The murine macrophage-derived cell line P388D1 secretes the lymphokine inter-leukin 1 (IL-1) when stimulated by a variety of agents. When stimulated by bacterial lipopolysaccharide (LPS) the cells release IL-1 in both high and low molecular weight (m.w.) forms. The proportion of high m.w. IL-1 is reduced when IL-1-containing supernatants are concentrated by ammonium sulfate precipitation subsequent to hollow-fiber filtration. The high m.w. form can be converted to the low m.w. form by proteolysis, reduction and alkylation, or chromatography in a dissociating solvent. The low m.w. form remains as such, even when reconcentrated in fetal calf serum-containing medium. The high m.w. form thus likely consists of a complex between low m.w. IL-1 and another protein secreted by the P388D1 cell line.
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    Journal of Cellular Biochemistry 26 (1984), S. 1-89 
    ISSN: 0730-2312
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 152
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    Journal of Cellular Biochemistry 26 (1984), S. 91-117 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 153
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    Journal of Morphology 179 (1984), S. 175-195 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: A histological investigation of the filtering function of the spleen of the sunfish Lepomis spp. was conducted by light, scanning, and transmission electron microscopy. The parenchyma of the organ is predominantly red pulp, a system of splenic cords and sinuses. The white pulp consists of loose lymphoid tissue which forms a cuff around the pulp arteries. Filtering of particulate matter from the blood occurs in the red pulp by phagocytes of the pulp cords and ellipsoids (periarterial macrophage sheaths). The ellipsoids are pale-staining cuffs of macrophages and reticular cells in a framework of reticular fibres surrounding the arterial capillaries. Destruction of effete blood cells (especially erythrocytes) is confined to the pigment nodules; particulate matter is not taken up by the nodules. These yellow-brown bodies are dispersed throughout the red pulp and are bounded by a reticular capsule. They contain masses of phagocytes and have the appearance of a morula. They are associated with blood vessels and are surrounded by sinusoids. Prussian Blue stain shows the presence of haemosiderin within their phagocytes. The phagocytes of the pigment nodules are filled with inclusions such as residual bodies, siderosomes, and fragments of erythrocytes. The early filtering of particulate matter by the phagocytes of the pulp cords and ellipsoids may allow for a more efficient phagocytosis of erythrocytes by the pigment nodules, followed by storage and reutilization of iron-containing compounds uncontaminated by other phagocytosed material.
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  • 154
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    Journal of Morphology 179 (1984) 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 155
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    Journal of Morphology 179 (1984), S. 197-202 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Upon germination of a statoblast, the shell is split into two valves; a mucous pad which represents the basal portion of the body wall of the incipient zooid or ancestrula then appears from between the valves; lastly, a tiny polypide evaginates at the opposite site. When two or more contiguously located statoblasts (floatoblasts or sessoblasts) of the same species germinate simultaneously, their mucous pads often come into contact with each other. The walls of the mucous pads then disappear in the contact areas, thus uniting the coeloms of the ancestrulae. This type of fusion between mucous pads of statoblast-derived ancestrulae was ascertained in Plumatella emarginata, P. repens, P. casmiana, and Hyalinella punctata. The fusion is clearly species specific, and shows no clone specificity or allogeneic recognition. The fusibility test reported here seems to be a useful method for the examination of conspecificity in plumatellid bryozoans.
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  • 156
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    Journal of Morphology 179 (1984), S. 203-228 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Integumentary development on the dorsal and ventral aspects of the body of 14, 21, 26, 33, and 40-day incubated embryos of the European Wall Lizard (Lacerta muralis) is described. While the earliest stages of epidermal differentiation resemble those reported for other tetrapods, precocious differentiation of dermal collagen more resembles that of anamniotes than that of birds and mammals. Anchoring complexes comprising cellular components, anchor filaments, and collagen are described, and their possible relationship to the formation of scale anlagen is discussed. The first embryonic epidermal generation differentiates beneath the periderm; most features of its histogenesis resemble those that have been described for the epidermis of adult squamates, but certain previously ignored organelles, including possible earlier β-keratin precursors, are reported. Different strategies regarding in ovo peridermal loss and posthatching shedding behavior are described and discussed in light of presently available data concerning control of cell differentiation in the squamate epidermis.
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  • 157
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    Journal of Morphology 182 (1984), S. 169-178 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: This investigation describes the morphogenesis of the type I pneumocyte from the neonatal stage to the age of 3 months. Cells lining subpleural air spaces were photographed from electron microscopic serial sections and a three-dimensional representation of each cell was obtained by transferring the contours of the cell membranes from micrographs to transparent plastic sheets which were then spaced to scale and stacked. The portion of the reconstructed cell surface taking part in the formation of the blood-airbarrier increased extensively in postnatal stages when compared with reconstructed cells of prenatal stages. Reconstructed cell-surface irregularities decrease during distension. A cytoplasmic plate seen in the last stage studied may represent a forming alveolar pore.
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  • 158
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    Journal of Morphology 182 (1984), S. 197-219 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Many climbing mammals are able to reverse normal hind foot posture to effect the grip necessary to descend headfirst or to hang upside down. Such hind foot reversal is known in sciurids, procyonids, felids, viverrids, tupaiids, prosimians, and marsupials. The joint movements involved, however, have never been documented unequivocally although various interpretations (some contradictory) have been made. We report here radiographic data from species of the genera Didelphis, Felis, Nasua, Nycticebus, Potos, Sciurus, and Tupaia. In the six eutherians studied, three joints are involved, and there is a common pattern in the mechanism: crurotalar plantarflexion, subtalar inversion, and transverse tarsal supination. Hind foot reversal represents the development of an unusual degree of excursion at these joints, rather than the appearance of any new type of movement. In Didelphis the mechanism is quite different: a bicondylar, spiral tibiotalar joint is the principal site of inversion/abduction movements. This specialization is characteristic of didelphids and phalangerids, and occurs in the extinct multituberculates as well; it is not found in macropodids (which are like eutherians in crurotalar joint structure) or other marsupial families. This diversity in pedal structure and function is evidently the result of parallel evolution from the type of tibiotalar joint of cynodonts and early mammals. In Morganucodon the bulbous, hemispheroidal proximal surface of the talus bears two tibial facets. These facets are represented in didelphids and multituberculates as sulci, whereas in macropodids and eutherians they developed as the proximal and medial surfaces of the talar trochlea. Among living mammals, the primitive hemispheroidal joint is retained among monotremes as a ball and socket joint.
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    Journal of Morphology 181 (1984), S. 21-28 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Shells from eggs of the turtle Kinosternon flavescens were examined during different stages of development with light and scanning electron microscopy. Prior to initiation of the calcareous layer, organic spheres or cores appear on the outer surface of the shell membrane. Presumably, these cores nucleate deposition of the mineral layer of the eggshell. Growing shell units of the mineral layer are rounded and nodular in shape, crystallites of adjacent shell units do not interlock, and numerous spaces occur between shell units. As growth continues, most of the spaces between shell units are obliterated, and shell units become more elongate in form. The calcareous layer of partially shelled eggs resembles the calcareous layer of flexible-shelled eggs of emydids and chelydrids. Eggshells assume the morphology typical of rigidshelled chelonian eggs only at an advanced stage of shell formation. These observations indicate that rigid and flexible eggshells may form by fundamentally similar mechanisms, with length of shell growth being the primary determinant of whether shells are flexible or rigid.
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  • 160
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    Journal of Morphology 181 (1984), S. 29-47 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The formation of somites, coelomic sacs, splanchnic mesoderm, fat bodies, circular system, gonads, and musculature in the embryo of the primitive moth, Neomicropteryx nipponensis Issiki, is described. The following paired somites are formed: the labral, antennal, intercalary, mandibular, maxillary, labial, three thoracic, and 11 abdominal. Small but distinct coelomic cavities appear in all these somites. Labral somites differentiate into the labral muscles, stomodaeal muscles, and dorsal dilator muscles of the pharynx. Antennal somites differentiate into the antennal muscles, aorta, and the ventral dilator muscles of the pharynx. Intercalary somites are short-lived, disintegrating to liberate many free cells into the yolk. The suboesophageal body is not formed. Mandibular somites differentiate into the mandibular flexor and extensor muscles. Maxillary and labial somites differentiate into the splanchnic mesoderm, fat bodies, and into muscles of the maxillolabial region. Three pairs of thoracic and ten pairs of abdominal somites split into the splanchric and somatic mesoderm. The 11th abdominal somites merge into the proctodaeal mesoderm, and differentiate into the musculature of the hindgut. The heart is formed by the fusion of the cardioblasts derived from the first thoracic to the tenth abdominal segment. The aorta arises from the antennal median mesoderm. Blood cells are derived from the median mesodermal cells of the maxillary to the tenth abdominal segment. Germ cells appear at the mediodorsal corner of each somite in the fifth abdominal segment. They become enclosed with a mesodermal sheath to form a pair of rudimentary gonads in this segment. Major muscles in the head, thorax, and abdomen of the fully grown embryo are described.
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    Journal of Morphology 181 (1984), S. 49-68 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Histological techniques and paraldehyde-fuchsin (PAF) staining were used to study the synganglion and to locate neurosecretory regions and neurosecretion within the synganglion of the chicken mite, Dermanyssus gallinae. The synganglion, which is formed internally by neuropilar ganglia, gives rise to a single esophageal and paired cheliceral, palpal, pedal (I-IV), and opisthosomal nerves. The neuropilar ganglia are interconnected by commissures and connectives within the synganglion. Twelve PAF-positive neurosecretory regions are present in unfed protonymphs, unfed deutonymphs, virgin males and females, and mated males. There are 11 PAF-positive neurosecretory regions in larvae, 24-72 hours post-fed deutonymphs and mated females. Neurosecretory regions in these developmental stadia are described in relation to their positions adjacent to individual neuropilar ganglia.
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  • 162
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    Journal of Morphology 181 (1984), S. 69-86 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Hymenopteran venom glands are epidermal glands that have evolved from female accessory reproductive glands. In the honey bee, Apis mellifera L., the venom gland shows many of the fine structural features of primitive glands. A honey bee venom gland is a simple, long, thin, distally bifurcated structure, opening into an ovoid reservoir. Along most of the length of the gland are similar secretory units that have four major components (secretory cells, duct cells, ducts, and end apparatuses), except in the part of the gland proximal to the venom reservoir, where the secretory units resemble those around the venom reservoir. In the latter secretory units a funnel structure occurs between the duct (which is shorter than that of the secretory units of the gland) and the end apparatus. This funnel may be important in protecting the secretory cells around the reservoir from the cytolytic activity of the complex chemical mixture constituting the venom.
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  • 163
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    Journal of Morphology 181 (1984), S. 87-95 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: In Necturus maculosus the organization of the interstitial tissue varies according to the stage of spermatogenesis. Leydig cells at various stages of differentiation and myoid cells are always present in this tissue. The Leydig cells are undifferentiated at all phases of germ cell activity and only hypertrophy following spermiation and degeneration of Sertoli cells. These Leydig cells are structurally analogous to mammalian Leydig cells. They do not form part of the lamina propria of the seminiferous lobules and hence cannot be referred to as lobule-boundary cells previously described in the urodele testis (Lofts, '74). When the Leydig cells hypertrophy, numerous unmyelinated axons appear in the interstitial tissue. These axons, often devoid of Schwann-cell cytoplasm, occur in close proximity to Leydig cells. Because the levels of both Substance P and neurotensin increased in the testis of Necturus maculosus as Leydig cells differentiated, we concluded that these neural elements may regulate Leydig-cell function locally, through the release of neuropeptides.
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  • 165
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    Journal of Morphology 181 (1984), S. 97-131 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Topics: Biology , Medicine
    Notes: The three-dimensional structure of the organ of Bellonci in the marine amphipod Gammarus setosus and the relationship between its sensory cells and concretion are described using light, transmission, and scanning electron microscopy, with chemical treatment for cell lysis, calcium chelation, glycogen staining, and lanthanum labelling. The organ is encapsulated and has three units called fuselli. Each is enclosed by two fusellar cells which generate and release calcium granule strands into the cores of the fusellar concretions, which are united in the center of the organ. The surface of each fusellus is traversed by spiral dendrites entering dorsally and ending ventrally. The spiral dendrites arise from sensory neurons contained in a palm-shaped ganglion in the center of the capsule, beyond which they are twisted like a rope before reaching the concretion. The spiral dendrites are linked in pairs by gap and tight junctions and each gives origin to two pairs of 9+0 sensory cilia 30 μm apart. The ciliary distal segments give rise to long tubules which are in contact with the calcium granule strands. The ciliary proximal segments are expanded by many long mitochondria which interdigitate with the branched striated ciliary rootlets. The concretion is suspended in the capsule cavity by axons originating from four neurons of a remote mechanoreceptor. The structure of the organ suggests that it is a sensory organ involved in the reception and integration of a variety of stimuli.
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    Journal of Morphology 181 (1984), S. 133-142 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The respiratory system of Ocypode cordimanus consists of seven pairs of gills, modified for aerial gas exchange, and a single pair of lungs. Each lung is formed from the inner surface of the branchiostegite and the thoracic wall of the branchial chamber. The branchiostegal surface is increased by a fleshy infolding, the branchiostegal shelf, whilst the surface area of the thoracic lung wall is enhanced by a large flaplike fold.The anatomy of the major sinus systems and the vascular supply to the lungs were investigated. Venous hemolymph is supplied to the lungs potentially from all the major body sinuses. The dorsal, ventral, hepatic, and infrabranchial sinuses are all connected anteriorly to the two eye sinuses which distribute hemolymph to the lungs. Each eye sinus gives off five branches to the branchiostegal lung surface and one to the thoracic lung wall. These afferent vessels are highly branched and interdigitate closely with efferent vessels. The two systems are connected by flat lacunae lying just beneath the respiratory epithelium and these are believed to be the site of gas exchange. The efferent vessels empty into two pulmonary veins on each side, one serving the branchiostegal lung wall and the other the thoracic wall. The two vessels on each side fuse before joining the pericardial cavity as a single trunk on each side.
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    Notes: Motor units of the medial gastrocnemius (MG) and the single lateral gastrocnemius/soleus (LG/S) muscles of the opssum (Didelphis virginiana) were found to have uniformly slow contraction times relative to homologous muscles of the cat. Though a broad range of peak tetanic tensions was found among motor units from both muscles, most of the motor units were quite large relative to tension of the whole muscle. Comparison of the relative sizes of motor units showed that those of LG/S are significantly larger and slower than the units of MG. This suggests that the motor units of the two muscles may be differentially recurited during different behaviors.All of the MG and LG/S motor units were highly or moderately resistant to fatigue. Histochemical staining for NADH-diaphorase activity indicated consistently high levels of the enzyme in all of the fibers of both muscles. Apparently, all of the fast motor units consist of fast oxidative/glycolytic (FOG)-type muscle fibers. Our data provide functional evidence that the types of myofibrillar ATPase demonstrated by Brooke and Kaiser ('70), are not necessarily correlated to physiological classification of fiber types as slow oxidative (SO), fast oxidative/glycolytic (FOG), and fast glycolytic (FG) (Peter et al., '72).Perhaps compartmentalization of muscle fiber types may be a first step in the separation of muscles into multiple heads during the evolution of specialization to diverse locomotor habits among the mammals.
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  • 168
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    Journal of Morphology 182 (1984) 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 169
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    Journal of Morphology 181 (1984), S. 319-331 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The telencephalic medial wall of the lizard Psammodromus algirus was studied using Golgi and conventional light microscopic techniques. The area is formed by two different cytological fields - medial cortex and dorsomedial cortex. These two cortices possess three layers dorsoventrally: a superficial plexiform layer, a cellular layer, and a deep plexiform layer. The alveus, a deep fiber system, runs adjacent to the ependyma. Four classes of neurons are found in the cellular layer of the medial cortex on the basis of soma shape, dendritic pattern, and position in the layer: horizontal, double pyramidal, and candelabra cells. Solitary cells are present in the superficial and deep plexiform layers of the medial cortex. Those of the superficial plexiform layer are stellate cells. Horizontal and vertical cells are found in the deep plexiform layer. Double pyramidal cells are the most frequently impregnated in the cellular layer of the dorsomedial cortex. In addition, candelabra cells are present at the lateral end of the layer. Two cell types are found in the deep plexiform layer of the dorsomedial cortex: solitary pyramidal cells and, among the fibers of the alveus, horizontal cells. Ependymal tanycytes line the ventricular surface, and protoplasmic astrocytes are found in the plexiform layers of both medial and dorsomedial cortices.
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  • 170
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    Journal of Morphology 182 (1984), S. 95-113 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: A three-dimensional muscle model with complex geometry is described and tested against experimental data. Using this model, several muscles were constructed. These muscles have equal optimum length but differ in architecture. The force exerted by the constructed muscles, in relation to their actual length and velocity of shortening, is discussed. Generally speaking, the constructed muscles with considerable pennation have great fiber angles, a great physiological cross section, a narrow active and steep passive length-force relation, and a low maximal velocity of shortening. The maximal power (force times velocity) delivered by the constructed muscles is shown to be almost independent of the architecture of the muscles. The steepness of the passive length-force relation is determined mainly by the shortest fibers within the group of constructed muscles, wheras maximal velocity of shortening and the width of the active length-force relation are determined mainly by the longest fibers.The validity of the three-dimensional muscle model with respect to some morphological and functional characteristics is tested. Length-force relations of constructed muscles are compared with the actual length-force relations of mm. gastrocnemii mediales and mm. semimembranosi of male Wistar rats. Moreover, actual fiber angle, fiber length, and muscle thickness of three mm. gastrocnemii mediales are compared with values found for constructed muscles. It is concluded that the three-dimensional muscle model closely approximates the actual muscle form and function.
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  • 171
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    Journal of Morphology 182 (1984), S. 125-136 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Horseradish peroxidase histochemical studies of afferent and efferent projections of the trigeminal nerve in two species of chondrostean fishes revealed medial, descending and ascending projections. Entering fibers of the trigeminal sensory root project medially to terminate in the medial trigeminal nucleus, located along the medial wall of the rostral medulla. Other entering sensory fibers turn caudally within the medulla, forming the trigeminal spinal tract, and terminate within the descending trigeminal nucleus. The descending trigeminal nucleus consists of dorsal (DTNd) and ventral (DTNv) components. Fibers of the trigeminal spinal tract descend through the lateral alar medulla and into the dorsolateral cervical spinal cord. Fibers exit the spinal tract throughout its length, projecting to the ventral descending trigeminal nucleus (DTNv) in the medulla and to the funicular nucleus at the obex. Retrograde transport of HRP through sensory root fibers also revealed an ascending bundle of fibers that constitutes the neurites of the mesencephalic trigeminal nucleus, cell bodies of which are located in the rostral optic tectum. Retrograde transport of HRP through motor root fibers labeled ipsilateral cells of the trigeminal motor nucleus, located in the rostral branchiomeric motor column.
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  • 172
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    Journal of Morphology 182 (1984), S. 137-152 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The epithelium of the posterior intestine and hindgut of recently metamorphosed adult lampreys (Petromyzon marinus L.) prior to and during spontaneous feeding was examined using light and electron microscopy. These two regions differ slightly in their general morphology but possess the same mucosal cell types. Included are caveolated absorptive and mucous cells, which are not present in more cephalic regions of the intestine, and ciliated and enteroendocrine cells. During feeding, the caveolated cells undergo dramatic transformation in their structure, namely, through the acquisition of numerous heterophagic vacuoles. Due to their morphology and to the fact that there are low amounts of lipid, it is suspected that caveolated cells are primarily involved in the absorption of protein components from the ingested host blood and body fluids. Iron in caveolated cells may result from the degradation of ingested heme or reflect the excretion of bile products at this location in the intestine. Mucous cells are likely responsible for lubrication of the luminal surface and may be important as a stem cell for the mucosal epithelium.
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  • 173
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    Journal of Morphology 180 (1984) 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 174
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    Journal of Morphology 180 (1984), S. 55-68 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Topics: Biology , Medicine
    Notes: A comparative study of the forelimbs of the semifossorial prairie dog, Cynomys gunnisoni, and the scansorial tree squirrel, Sciurus niger, was focused on the musculoskeletal design for digging in the former and climbing in the latter. Based on lever arm mechanics, it was expected that the forelimb of the prairie dog would show features appropriate to the production of relatively large forces and that of the fox squirrel to relatively great velocity. Force and lever arm measurements were made of select forelimb muscles at the shoulder, elbow, and wrist joints for a series of angles in both species. Contraction time and fatigue indexes were determined for the same forelimb muscles. Contrary to expectation, in the few cases in which significant (P 〈 .05) differences were found, the forces, lever arms, and torques (force times its lever arm) were greater in the smaller fox squirrel. The observed variation in the torques produced fits the demands on the forelimb during climbing and digging as estimated from films. Several forelimb muscles of the fox squirrel show significantly higher mean contraction times than do the homologous muscles of the prairie dog. There were no significant differences between the two species in the fatigability of the selected forelimb muscles, although the mean fatigue index was always higher (less fatigable muscle) in the prairie dog. Similarities in the forelimbs of these two sciurids suggest that only minor modifications may have been required of the ancestral forelimb in order for descendent forms to operate successfully as climbers and diggers.
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  • 175
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    Journal of Morphology 180 (1984), S. 297-308 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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    Topics: Biology , Medicine
    Notes: During the breeding season, male anurans display clasping behavior by holding females with their forelimbs. This behavior is peculiar to males, and may require specializations in forelimb musculature. The present study revealed that five kinds of forelimb muscles were heavier in the male Japanese toad than in the female: the flexor carpi radialis (FCR), the flexor antibrachii medialis caput superius (FAMsup), the abductor indicis longus (AIL), the extensor carpi radialis caput superius (ECRsup), and the flexor antibrachii lateralis superficialis caput superius (FALSsup). In addition, one breast muscle, the coracoradialis (CR), was also heavier in males than in females. A quantitative analysis of muscle fibers processed for myosin ATPase activity showed that, in such “sexually dimorphic muscles” of the female, both fast (twitch) and slow (tonic) muscle fibers were of smaller diameter than in other forelimb muscles of both sexes (all male muscles plus “nondimorphic muscles” of the female). Moreover, both types of fibers were less numerous than in the corresponding muscles of the male. These results suggest that the “sexually dimorphic muscles” are used especially for clasping by the male and are degenerative or subnormal in the female. Slow muscle fibers were neither peculiar to, nor abundant in, these clasping muscles, although they may well be necessary for tonic and prolonged contractions of the forelimb muscles during clasping. The mechanism of sexual dimorphism may be a direct action of androgens on clasping muscles or an indirect action on clasping muscles via the innervating motoneurons.
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  • 176
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    Journal of Cellular Biochemistry 24 (1984) 
    ISSN: 0730-2312
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 177
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    Journal of Cellular Biochemistry 24 (1984), S. 297-306 
    ISSN: 0730-2312
    Keywords: Plasmodium knowlesi ; variant antigen ; schizont-infected erythrocyte ; detergents ; radioiodination ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Four detergents have been compared for identification of the Plasmodium knowlesi variant antigen on infected erythrocytes by immunoprecipitation analysis. Erythrocytes infected with late trophozoite and schizont forms of cloned asexual parasites were labeled by lactoperoxidase-catalyzed radioiodination and extracted either with the anionic detergents sodium dodecyl sulfate (SDS) or cholate, the neutral detergent Triton X-100, or the zwitterion 3-[(3-cholamidopropyl)di-methylammonio]-1-propane sulfonate (CHAPS). After addition of Triton X-100 to SDS and cholate extracts, parallel immunoprecipitations of the four extracts were performed using rhesus monkey antisera of defined agglutinability. Identical results were obtained with clone Pkl(A+ ), which has 125I-variant antigens of Mr 210,000 and 190,000, and with clone Pkl(B+)l+, which hasvariant antigens of Mr 200,000-205,000. SDS yielded maximal levels of immunoprecipitated 125I-variant antigens. Variant-specific immunoprecipitation was detected in some experiments with Triton X-100 and cholic acid but with significantly lower recovery than with SDS. CHAPS extraction did not yield the variant antigens on immunoprecipitation. The variant antigens could also be identified in Triton X-100-insoluble material by subsequent extraction with SDS, indicating that failure to recover these proteins in the Triton X-100-soluble fraction is due to failure of this detergent to extract the variant antigens rather than to degradation during extraction. We suggest that the 125I-variant antigens either have a structure that renders them intrinsically insoluble in Triton X-100, cholate, or CHAPS, or that they are associated in some way with host cell membrane components that also resist solubilization by these detergents.
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  • 178
    ISSN: 0730-2312
    Keywords: mRNA levels ; regulation of biosynthesis ; light-harvesting chlorophyll a/b complex ; chloroplast ; ribulose bisphosphate carboxylase ; oxygenase ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The photoregulation of chloroplast development in pea leaves has been studied by reference to three polypeptides and their mRNAs. The polypeptides were the large subunit (LSU) and the small subunit (SSU) of ribulose 1,5-bisphosphate carbox-ylase/oxygenase (RUBISCO), and the light-harvesting chlorophyll a/b protein (LHCP). The polypeptides were assayed by a sensitive radioimmune assay, and the mRNAs were assayed by hybridization to cloned DNA probes. LSU, LSU mRNA, and LHCP mRNA were detectable in etiolated seedlings but LHCP, SSU, and SSU mRNA were at or below the limit of detection. During the first 48 hr of de-etiolation under continuous white light, the mRNAs for LSU, SSU, and LHCP increased in concentration per apical bud by about 40-fold, at least 200-fold, and about 25-fold, respectively, while the total RNA content per apical bud increased only 3.5-fold. In the same period, the LSU, SSU, and LHCP contents per bud increased at least 60-, 100-, and 200-fold, respectively. The LHCP increased steadily in concentration during de-etiolation, whereas the accumulation LSU, SSU, and SSU mRNA showed a 24-hr lag. The accumulation of SSU, SSU mRNA, and LHCP mRNA showed classical red/far-red reversibility, indicating the involvement of phytochrome in the regulatory mechanism. LSU and LSU mRNA were induced equally well by red and far-red light. The LHCP failed to accumulate except under continuous illumination. These results indicate that the accumulation of SSU is controlled largely through the steady-state level of its mRNA, which is in turn almost totally dependent on light as an inducer and on phytochrome as one of the photoreceptors. The accumulation of LSU is largely but not totally determined by the level of its mRNA, which appears to be under strong photoregulation, which has yet to be shown to involve phytochrome. Phytochrome is involved in the regulation of LHCP mRNA levels but substantial levels of the mRNA also occur in the dark. LHCP accumulation is not primarily governed by the levels of LHCP mRNA but by posttranslational stabilization in which chlorophyll synthesis plays a necessary but not sufficient role.
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  • 179
    ISSN: 0730-2312
    Keywords: N-substituted p-benzoquinone imines ; Trypanosoma brucei brucei ; trypanocidal drugs ; Hansch approach ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: It has previously been found that naphthoquinones can potentiate the rate of hydrogen peroxide production by mitochondrial preparations of Trypanosoma brucei brucei and that organisms treated with naphthoquinones are more susceptible to lysis, especially in the presence of compounds such as heme, which promote the homolytic cleavage of hydrogen peroxide. We have evaluated the lytic effect of various N-substituted p-benzoquinone imines both in vitro and in vivo and have attempted to correlate their structure with trypanocidal activity using the Hansch approach. While none of the compounds tested proved to be active in vivo, all caused the lysis of trypanosomes in vitro. The parameters that correlated best with trypanocidal activity were the conditional redox potential, the lipophilicity of the substituent attached to the nitrogen atom and the number of active hydrogens on the quinoncid ring. These findings suggest two possible modes of action, which may in fact be related. Conjugate nucleophilic addition and/or oxidative damage could be responsible for lysis of the parasites. These same compounds were previously found to be active against the ascitic sarcoma 180 in mice. The strong correlation between antineoplastic activity in vivo and trypanocidal activity in vitro suggests a similar mode of action in both cases. Further studies aimed at developing a quinonelike compound that will be active against trypanosomes in vivo are now in progress.
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  • 180
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    Journal of Cellular Biochemistry 25 (1984), S. 31-43 
    ISSN: 0730-2312
    Keywords: intercellular adhesion ; Dictyostelium discoideum ; discoidin I ; antibodies ; antidiscoidin I Fab fragments ; in vitro reaggregation ; morphogenesis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Antibodies against pure discoidin I have been used as a tool to ascertain the role of this lectin in aggregation of Dictyostelium discoideum. Discoidin I is widely expressed over the cell surface of aggregation-competent AX-2 cells, as ascertained by indirect immunofluorescence with specific (antidiscoidin I) antibodies. Univalent antidiscoidin I antibodies (Fab fragments) inhibit the aggregation-specific intercellular adhesion of D discoideum AX-2 cells in an in vitro assay. This inhibition depends on antibody concentration and cell density; a 50% inhibition of cell aggregation was obtained at antidiscoidin I Fab concentration of 4.5 mg/ml and 1 × 106 cells/ml. Aggregation and morphogenesis on solid support is also effectively inhibited when AX-2 cells are starved in the presence of antidiscoidin I Fab fragments. The inhibition of morphogenesis is also dose dependent and more effective than in the in vitro assay. No inhibition of aggregation either in the in vitro assay or on morphogenesis on solid support was observed with preimmune Fab fragments at any of the concentrations tested (up to 9.6 mg/ml).
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  • 181
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    Journal of Cellular Biochemistry 25 (1984), S. 45-59 
    ISSN: 0730-2312
    Keywords: epidermal growth factor ; heterogeneity ; immunosuppressive activity ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The suppression of antibody formation to sheep red cells in mice by partially purified fractions of mouse submaxillary gland [7] was shown to be caused by epidermal growth factor (EGF). Purification of EGF by the method of Savage and Cohen [11] resolved three components referred to as EGF a, EGF b, and EGF c. All three induced premature eye opening in neonatal mice, but only EGF a (identified as EGF1-53 ) had full immunosuppressive activity. EGF c was shown by micropeptide mapping of chymotryptic and thermolytic digests and aminoterminal analysis to differ from EGF a only by the presence of β-aspartyl instead of an asparaginyl residue. EGF b differed from EGF a in that it lacked the N-terminal asparagine. EGF shortened enzymatically at its carboxy terminal by two or five amino acids did not have any immunosuppressive activity. These findings-suggest that, in contrast to some other biological effects of EGF, intact amino and carboxy terminals are required for the expression of immunosuppressive activity.
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  • 182
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    Journal of Cellular Biochemistry 25 (1984) 
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    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 183
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    Journal of Cellular Biochemistry 25 (1984), S. 61-72 
    ISSN: 0730-2312
    Keywords: hypertonic cryohemolysis ; hypotonic hemolysis ; thermotropic membrane processes ; membrane structure-function relationship ; erythrocyte membrane treatments ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The hypothesis of a correlation between the effects of temperature on red blood cells hypotonic hemolysis and hypertonic cryoheniolysis and two thermotropic structural transitions evidenced by EPR studies has been tested. Hypertonic cryoheniolysis of red blood cells shows critical temperatures at 7°C and 19°C. In hypotonic solution, the osmotic resistance increases near 10°C and levels off above 20°C. EPR studies of red blood cell membrane of a 16-dinyloxyl stearic acid spin label show, in the 0-50°C range, the presence of three thermotropic transitions at 8, 20, and 40°C. Treatments of red blood cells with acidic or alkaline pH, glutaraldehyde, and chlorpromazine abolish hypertonic cryoheniolysis and reduce the effect of temperature on hypotonic hemolysis. 16-Dinyloxyl stearic acid spectra of red blood cells treated with glutaraldehyde and chlorpromazine show the disappearance of the 8°C transition. Both the 8°C and the 20°C transitions were abolished by acidic pH treatment. The correlation between the temperature dependence of red blood cell lysis and thermotropic breaks might be indicative of the presence of structural transitions producing areas of mismatching between differently ordered membrane components where the osmotic resistance is decreased.
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  • 184
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    Journal of Cellular Biochemistry 25 (1984), S. 87-97 
    ISSN: 0730-2312
    Keywords: macrophagelike cell ; cholesterol auxotroph ; growth ; sterol structure ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The lipid requirements of a human macrophagelike cell line were studied. The cells grew only about one generation in a medium supplemented with delipidated serum; during the growth the cholesterol content of the cells was depleted. Growth was restored by including in the medium serum lipids subjected to alkaline hydrolysis or cholesterol. The extent of growth was dependent on cholesterol concentration. No growth was obtained with 5-cholestene, 5-cholesten-3-one, cholesteryl chloride, coprostanol, β-sitosterol, orstigmasterol. Very limited growth occurred with cholesterol methylether, epicholesterol, or β-cholestarol. Therefore, for optimal growth of these cells there is a stringent requirement for the structural features of cholesterol, which include a 3-βOH group, a Δ5 -double bond, a trans ring A/B configuration, and freedom of the side chain from bulky groups. This stringency far exceeds what was previously reported for other cells. Of the six sterols that failed to support growth at all, five were incorporated into cells moderately to extensively. This suggests that assembly of a functional membrane is impaired when these sterols are used as substrates for growth.
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  • 185
    ISSN: 0730-2312
    Keywords: spin-labeling of erythrocyte membrane ; membrane structural transitions ; protein-lipid interactions ; membrane organization ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The relationship between membrane structural properties and functions has been generally inferred from observed thermotropic phenomena. By the use of 16-dinyloxyl stearic acid spin probe we investigated the red blood cell membrane components involved in three characteristic thermotropic structural transitions occurring at 8, 20, and 40°C. The transition at 8°C is removed by chymotrypsin treatment at the cytoplasmic membrane layer. The 20°C phase transition is unmodified after chymotrypsin treatment and occurs at 15°C after complete proteolysis of intramembranc chymolrypsin insensitive peptides. Liposomes from the total lipid extract of RBC show only one thermotropic transition at 15°C. The 40°C phase transition is absent in vesicles free of skeletal proteins, in vesicles obtained after RBC storage, and in low-ionic-strength resealed ghosts. Transitions at 8°C and 40°C appear to be due to the interactions of cytoplasmic exposed proteins with membrane, whereas the 20°C transition is intrinsic to the lipid component.
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  • 186
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    Journal of Cellular Biochemistry 25 (1984), S. 99-107 
    ISSN: 0730-2312
    Keywords: calmodulin ; calmodulin acceptor protein ; calcimedins ; sperm acrosome ; antibody localization ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: A calmodulin acceptor protein has been identified in isolated hamster caudal sperm by immunofluoresence and Western transfer techniques. The protein shows a localization in sperm heads identical to calmodulin. Fluorescence of both calmodulin and the acceptor protein are lost by treatment with MgCl2, conditions which release the acrosome. These results are consistent with the proposed function of calmodulin in a sperm function.
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  • 187
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    Journal of Cellular Biochemistry 25 (1984) 
    ISSN: 0730-2312
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 188
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    Journal of Cellular Biochemistry 25 (1984), S. 109-121 
    ISSN: 0730-2312
    Keywords: adhesion ; cell surface glycoprotein ; monoclonal antibodies ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Two monoclonal antibodies that cause changes in the morphology of cultured chick myogenic cells have been described previously [8]. In this paper, these antibodies are shown to interact with the same 140Kd protein. The 140Kd protein has been further characterized as a cell-surface glycoprotein by lactoperoxidase-catalyzed iodinations and lectin affinity chromatography. The protein is resistant to digestion by trypsin and collagenase and has been shown to be unrelated to fibronectin by immunoprecipitation studies and by peptide mapping. A second protein, of approximately 170Kd MW; is also immunoprecipitated by the monoclonal antibodies. This protein is probably unrelated to the 140Kd protein since the peptide maps are quite distinct.
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  • 189
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    Journal of Cellular Biochemistry 25 (1984), S. 123-129 
    ISSN: 0730-2312
    Keywords: cultured muscle ; protein synthesis ; amino acid pools ; ferritin synthesis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Compartmentalization of cellular amino acid pools occurs in cultures of cardiac and skeletal muscle cells, but the factors involved in this are not clear. We have further defined this problem by analyzing the intracellular free leucine and the transfer-RNA-(tRNA)-bound leucine pool in cultures of skeletal and cardiac muscle incubated with 3H-leucine in the presence and absence of serum and amino acids. Withdrawal of nitrogen substrates caused substantial changes in leucine pool relationships-in particular, a change in the degree to which intracellular free leucine and tRNA-leucine were derived from the culture medium. In separate experiments, the validity of our tRNA measurements was confirmed by measurements of the specific activity of newly synthesized ferritin after iron induction. We discuss the implications of these findings with regard-to factors involved in the control of amino acid flux through the cell, as well as with regard to design of experiments using isotopic amino acids to measure rates of amino acid utilization.
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  • 190
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    Journal of Cellular Biochemistry 26 (1984), S. 75-81 
    ISSN: 0730-2312
    Keywords: actyl-CoA carboxylase ; HL-60 ; differentiation ; leukemia ; fatty acid ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: In order to better understand the mechanism by which changes in the fatty acid composition of cellular lipids occur in leukemia cell lines induced to differentiate, the activity of the first enzyme of fatty acid biosynthesis, acetyl-CoA carboxylase (EC 6.4.1.2) was measured in HL-60 promyclocytic leukemia cells before, during and after treatment with compounds that induce these cells to mature to neutro-phillike cells. After 24 h of exposure to dimethylsulfoxide, retinoic acid, or butyric acid, no morphological or biochemical (nitroblue tetrazolium reduction) evidence of differentiation occurred, but acetyl-CoA carboxylase activity decreased 44, 44.5, and 49% respectively, compared to untreated cells. After 7 days of culture in the presence of these agents, 79, 83, and 72% of cells acquired the ability to reduce nitroblue tetrazolium (versus 15% of control cells) and enzyme activity decreased 92.7, 99.7, and 98%, compared to control cultures, with the three compounds respectively. Thus, some of the reported changes in fatty acid composition of leukemia cells with differentiation may arise, in part, from the depression of the de novo fatty acid biosynthetic pathway and the loss of acetyl-CoA carboxylase activity may be a useful marker for neutrophilic differentiation in HL-60 cells.
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  • 191
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    Journal of Cellular Biochemistry 26 (1984), S. 83-93 
    ISSN: 0730-2312
    Keywords: DNA binding protein ; polyoma virus ; moddle-T ; retroviruses ; oncogenes ; transforming proteins ; SV40 large-T ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Cellular oncogenes and their activated and retrovirus-coded counterparts play an important role in cellular regulation. Here the relationship between such oncogenes and the genes coding for the transforming proteins of the papovaviruses, polyoma viruses, and simian virus 40 (SV40) is discussed. It is concluded that polyoma virus may transform established cells by a mechanism involving activation of a cellular oncogene product, whereas SV40 may transform by a mechanism involving a previously little studied cytoplasmic form of the transforming protein.
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  • 192
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    Journal of Cellular Biochemistry 26 (1984), S. 107-116 
    ISSN: 0730-2312
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
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  • 193
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    Journal of Cellular Biochemistry 26 (1984), S. 95-106 
    ISSN: 0730-2312
    Keywords: RSV src protein ; retrovirus transformation ; tyrosine phosphorylation ; protein kinase ; vanadium ion ; oncoprotein ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The transforming protein of Rous sarcoma virus (RSV) typically appears as a single phosphorylated polypeptide designated pp60v-src, pp60v-src possesses a protein kinase activity specific for tyrosine residues on select protein substrates. Treatment of RSV-transformed cells with vanadium ions resulted in the appearance of an electrophoretic variant of pp60v-src and was paralleled by a significant increase in the src kinase specific activity in purified enzyme preparations. Both the normal (standard) src kinase and the src kinase preparations obtained from vanadium-treated cells exhibited similar optimal activity profiles for MgCl2, KCl, and pH. Furthermore, their site specificities of phosphorylation of the substrates casein and vinculin were the same. The reaction kinetic profile of the standard src kinase showed a nonlinear pattern, while the vanadium enzyme exhibited conventional linear Michaelis-Menten kinetics. These results are discussed with respect to the possible functional regulation of pp60v-src activity by a vanadium-sensitive protein phosphatase activity.
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  • 194
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    Journal of Cellular Biochemistry 26 (1984) 
    ISSN: 0730-2312
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
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  • 195
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    Journal of Cellular Biochemistry 26 (1984), S. 117-125 
    ISSN: 0730-2312
    Keywords: gene expression ; amelogenins ; cDNA ; type II cells ; pulmonary surfactant ; ameloblasts ; epithelial differentiation ; regional mesenchymal specificity ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: One of the major problems in developmental biology concerns how differential gene activity is regionally controlled. One approach to this problem is the use of mesenchyme specification of epithelial-specific gene expression, such as, during tooth morphogenesis or lung morphogenesis. In the example of tooth morphogenesis, dental papilla ectomcsenchyme induces de novo gene expression as assayed by detection of amelogenin transcripts, or immunodetection of amelogenin poly-peptidcs within ameloblast cells. This process does not require serum supplementation or exogenous factors during epithelial-mesenchymal interactions in vitro. In contrast, lung morphogenesis requires hormones to mediate mesenchyme-derived influences upon type II epithelial cell differentiation and the production of pulmonary surfactant (eg, neutral and phospholipids, surfactant proteins). Glucocorticoids are required to stimulate the release of fetal pneumonocyte factor (FPF) from fibroblasts which, in turn, enhance the production of pulmonary surfactant. Thy-roxin appears to regulate the relative responsiveness of progenitor type II cells to steroid-stimulated release of FPF. This review will highlight key concepts associated with these developing organ systems and emphasize the problem of regional controls which regulate epithelial cell-specific gene activity.
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  • 196
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    Journal of Cellular Biochemistry 26 (1984), S. 135-146 
    ISSN: 0730-2312
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
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  • 197
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    Journal of Cellular Biochemistry 26 (1984), S. 127-133 
    ISSN: 0730-2312
    Keywords: radioimmunoassay ; superior cervical ganglion ; heparin sulfate ; transsynaptic regulation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The effect of neonatal deafferentation on the expression of a neuronal cell surface heparan sulfate proteoglycan (HeS-PG) was investigated in the developing rat superior cervical ganglion. Two monoclonal antibodies, one directed against the core protein of HeS-PG, and one to a determinant associated with a heparan sulfate side-chain, were used to monitor postnatal increases of HeS-PG by ra-dioiminunoassay. Following neonatal deafferentation by section of the cervical sympathetic trunk, total protein per ganglion was slightly reduced at survival times of 7, 14, and 30 days. Expression of the core protein determinant on HeS-PG was not altered in deafferented ganglia. In contrast, levels of side-chain determinant were significantly reduced at 14 and 30 days. These results suggest that processing of HeS-PG side-chains by principal ganglionic neurons is partially regulated by transsynaptic influences during development. Transsynaptic regulation of neuronal development may be a more general process than was believed previously, with effects not limited to molecules associated with synaptic development.
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  • 198
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    Journal of Cellular Biochemistry 26 (1984), S. 147-156 
    ISSN: 0730-2312
    Keywords: VIP ; oligodeoxynucleotides ; mRNAs ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: To understand the regulation of the production of peptide hormones, it is vital to elucidate their biosynthetic pathways. We chose to study a major regulatory peptide, vasoactive intestinal peptide (VIP), a peptide possessing both neurotransmitter and neurohormone actions. To identify the specific peptide mRNA we are using, as hybridization probes, radiolabeled synthetic oligodcoxynucleotides with sequence complementary to the predicted peptide mRNA sequence. Employing this approach, we identified and partially purified a ∼ 1600-base long mRNA containing VIP related sequences which can be translated in vitro into VIP-immunoreactive polypeptides. Such mRNA was detected in normal VIP producing tissue (rat brain), as well as in a tumor producing VIP (human buccal tumor). This mRNA differs in size from a known VIP-mRNA identified in human neuro-blastoma cells, suggesting the possibility of different VIP-mRNAs in different cell types.
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  • 199
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    Journal of Cellular Biochemistry 26 (1984), S. 169-179 
    ISSN: 0730-2312
    Keywords: insulin receptor ; tyrosine kinase ; pp60src ; phosphorylation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Both the insulin receptor and the gene product of the Rous sarcoma virus, pp60src, are protein kinases which phosphorylate themselves and other proteins on tyrosinc residues. Addition of the solubilized insulin receptor to purified pp60src increased the phosphorylation of the β-subunit of the insulin receptor. Phosphorylation of the insulin receptor by pp60src occurred both in the absence and presence of insulin but did not alter the insulin dose response for autophosphorylation of the receptor. Increasing concentrations of pp60src increased the phosphorylation of the receptor and at high concentrations equaled the maximal effect produced by insulin. Our observations suggest a possible mechanism by which the metabolically regulated insulin receptor tyrosine kinase could be altered by other tyrosine kinases such as that associated with pp60src. Further studies will be required to determine if the insulin receptor is phosphorylated by pp60src in Rous sarcoma virus-infected cells.
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  • 200
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    Journal of Cellular Biochemistry 26 (1984), S. 157-167 
    ISSN: 0730-2312
    Keywords: proteinase inhibitors ; alpha-1-antichymotrypsin ; breast epithelial cells ; matrix protection ; gp 68 ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The major glycoproteins synthesized by human breast epithelial cells have been characterized [6,8]. The most consistently observed and prominent component in supernatants of organ cultures of breast surgical specimens and of MCF-7 cells was gp 68 which has been immunologically identified as α-1-antichymotrypsin (Achy). In the present study we demonstrate that this glycoprotein can form an irreversible complex with chymotrypsin, which indicates that it is a functional inhibitor. The 14C-glucosamine-labeled gp 68 forms a stable, 88,000-dalton. enzyme-inhibitor complex with chymotrypsin. The molecule is secreted continuously for 9 days into a chemically defined, serum-free medium. In addition to the de novo synthesized inhibitor, another component is adsorbed from fetal bovine scrum and subsequently released into serum-free medium. This component also forms an irreversible, 88,000-dalton complex with enzyme. The observations establish that two types of inhibitors are associated with human breast epithelial cells, one actively synthesized and the other derived from serum. Both of these molecules may have significant roles in stabilizing cell surface components and in protecting extracellular matrices from untimely degradation.
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