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  • Ultrastructure
  • Springer  (29)
  • American Association for the Advancement of Science (AAAS)
  • American Institute of Physics (AIP)
  • 1990-1994  (29)
  • 1975-1979
  • 1960-1964
  • 1992  (29)
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Keywords
Publisher
  • Springer  (29)
  • American Association for the Advancement of Science (AAAS)
  • American Institute of Physics (AIP)
  • Wiley-Blackwell  (15)
Years
  • 1990-1994  (29)
  • 1975-1979
  • 1960-1964
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  • 1
    Electronic Resource
    Electronic Resource
    In vitro formation of mineralized nodules by periodontal ligament cells from the rat (1992)
    Springer
    Calcified tissue international 50 (1992), S. 459-467 
    Details
    ISSN: 1432-0827
    Keywords: Periodontal ligament fibroblast ; Mineralized nodule ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary The purposes of this study were to determine whether periodontal ligament (PDL) cells are capable of producing mineralized nodules in vitro and to analyze ultrastructural features of the nodules. Rat PDL cells were obtained from coagulum in the socket at 2 days after tooth extraction and cultured at confluence in standard medium containing Dulbecco's Modified Eagle's Medium supplemented with 10% FBS and antibiotics. To test mineralized nodule formation, cells were further cultured for an additional 3 weeks in the standard medium containing (1) ascorbic acid (50 μg/ml) and sodium β-glycerophosphate (10 mM), (2) ascorbic acid, sodium β-glycerophosphate, and dexamethasone (5 μM), or (3) ascorbic acid alone. Cells were then fixed in 2.5% glutaraldehyde, postfixed in 1% OsO4, and prepared for light and electron microscopy. Threedimensional nodules containing mineralized matrices were formed only when the cells were cultured in the presence of ascorbic acid and dexamethasone. They were composed of multilayered fibroblasts (up to 13 layers), and highly organized collagen fibrils with 64 nm cross-banding patterns between the cell layers. The fibroblasts in the nodules exhibited an elongated shape with a high degree of cytoplasmic polarity throughout the nodule, and have the morphological features of PDL fibroblasts as seen in vivo. Mineral deposition with needle-like crystals was initiated on collagen fibrils located in intercellular spaces of the upper cell layers and became increasingly heavier towards the bottom half of the nodules. X-ray microanalysis and electron diffraction analysis confirmed that mineral deposition contained calcium and phosphate in the form of immature hydroxyapatite. These nodules contained neither osteoblasts nor osteocytes, and have their own morphological organization and characteristics which differ from those formed by bone cells in culture. Therefore, these data suggest that PDL cells are capable of forming mineralized tissue in vitro with the morphological characteristics different from bone mineralized nodules.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00296778
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  • 2
    Electronic Resource
    Electronic Resource
    Early events during the establishment of the Gunnera/Nostoc symbiosis (1992)
    Springer
    Planta 188 (1992), S. 403-413 
    Details
    ISSN: 1432-2048
    Keywords: Cyanobacterium ; Gunnera ; Infection process ; Nostoc ; Symbiosis ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The symbiosis between Gunnera and Nostoc was reconstituted using G. chilensis Lam. and G. manicata Linden, respectively, and three different Nostoc strains. Six stages characterised by specific modifications in both the cyanobiont and the host were recognised during the infection process. Mucilage-secreting stem glands developed on the Gunnera stems independent of the presence of cyanobacteria (Stage I). Soon after addition of the Nostoc isolates to the plant apices, an abundant differentiation of motile hormogonia commenced. The cyanobacteria accumulated in the mucilage on the surface of the gland (Stage II), and the hormogonia then proceeded into the stem tissue through intercellular channels (Stage III). At the channel bases, Nostoc was detected between the cell walls of small, densely cytoplasmic Gunnera cells and also in elaborate folds of these (Stage IV). The Gunnera cell walls subsequently dissolved adjacent to the cyanobacteria and Nostoc entered the host cells (Stage V). Once the intracellular association was formed, a high proportion of the vegetative Nostoc cells differentiated into heterocysts (Stage VI). Nostoc changed from being rich in inclusions (particularly cyanophycin) while on the gland surface into a comparatively “non-storing” form during penetration and the early intracellular stages. Bacteria were numerous on the gland surface, fewer in the channels, and were never detected within the Gunnera cells, indicating the existence of specific recognition mechanisms discriminating between conceivable microsymbionts. Mechanisms behind mutual adaptations and interactions between the two symbionts are discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00192808
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  • 3
    Electronic Resource
    Electronic Resource
    High-pressure freezing of soybean nodules leads to an improved preservation of ultrastructure (1992)
    Springer
    Planta 188 (1992), S. 155-163 
    Details
    ISSN: 1432-2048
    Keywords: Bradyrhizobium ; Electron microscopy ; Glycine (root nodules) ; High-pressure freezing ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract High-pressure freezing of chemically untreated nodules of soybean (Glycine max (L.) Merr.), in sharp contrast to chemical fixation and prefixation, appears to preserve the ultrastructure close to the native state. This is supported by the observation that the peribacteroid membrane of high-pressure-frozen samples is tightly wrapped around the bacteroids, a finding that is fully consistent with the current views on the physiology of oxygen and metabolite transport between plant cytosol and bacteroids. In soybean root nodules, the plant tissue and the enclosed bacteria are so dissimilar that conventional aldehyde-fixation procedures are unable to preserve the overall native ultrastructure. This was demonstrated by high-pressure freezing of nodules that had been pre-fixed in glutaraldehyde at various buffer molalities: no buffer strength tested preserved all ultrastructural aspects that could be seen after high-pressure freezing of chemically untreated nodules.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00216809
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  • 4
    Electronic Resource
    Electronic Resource
    The microtubule cytoskeleton and the rounding of isolated generative cells ofNicotiana tabacum (1992)
    Springer
    Sexual plant reproduction 5 (1992), S. 64-71 
    Details
    ISSN: 1432-2145
    Keywords: Generative cell ; Isolation ; Microtubules ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Upon squashing of the pollen grain, the isolated generative cell ofNicotiana tabacum looses its spindle shape to become spherical; this phenomenon is independent of the sucrose concentration used. The time necessary for this change can vary from 1 min (0% sucrose) to 20 min (30% sucrose). The microtubular cytoskeleton was studied by means of immunofluorescence and electron microscopy. Just after isolation, 5 to 15 clearly visible bundles in microtubules organized in a basket-like structure are present. After 15 min in medium with 15% sucrose, the microtubular cytoskeleton disappears, and a diffusely spread tubulin can be observed. Neither the addition of 10–20 μM taxol to the medium, nor the omission of Ca2+ to the medium has any effect on the changes in cell shape and loss of microtubular bundles after isolation.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00714559
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  • 5
    Electronic Resource
    Electronic Resource
    Ultrastructure and microtubule organization of isolated generative cells ofAllemanda neriifolia at interphase and prophase (1992)
    Springer
    Sexual plant reproduction 5 (1992), S. 27-33 
    Details
    ISSN: 1432-2145
    Keywords: Isolated generative cells ; Ultrastructure ; Microtubule ; Immunofluorescence microscopy ; Allemanda neriifolia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The ultrastructure of isolated generative cells ofAllemanda neriifolia at interphase and prophase was studied. The microtubule organization of the isolated cells was also investigated by immunofluorescence microscopy with a monoclonal anti-α-tubulin. After the generative cells had been isolated from the growing pollen tubes by osmotic shock, most of the cells were at prophase and only a few were at interphase. The interphase cell is spindle shaped and contains an ellipsoidal nucleus. In addition to the usual organelles, the cytoplasm of the interphase cell contains numerous vesicles (each measuring 40–50 nm in diameter) and two sets of longitudinally oriented microtubule bundles — one in the cortical region and the other near the nucleus. Most of the prophase cells are spherical in shape. Based on the ultrastructure and the pattern of microtubule cytoskeleton organization three types of prophase cells can be recognized. (1) Early prophase cell, which contains the usual organelles, numerous vesicles, and a spherical nucleus with condensed chromosomes. Longitudinally oriented microtubule bundles can no longer be seen present in the early prophase cell. A new type of structure resembling a microtubule aggregate appears in the cytoplasm. (2) Mid prophase cell, which has a spherical nucleus containing chromosomes that appear more condensed than those seen in the early prophase cell. In addition to containing the usual organelles, the cytoplasm of this cell contains numerous apparently randomly oriented microtubules. Few vesicles are seen and microtubule aggregates are no longer present. (3) Late prophase cell, typified by the lack of a nuclear envelope. Consequently, the chromosomes become randomly scattered in the cytoplasm. Microtubules are still present and some become closely associated with the chromosomes. The changes in the ultrastructure and in the pattern of microtubule organization in the interphase and prophase cells are discussed in relation to the method of isolation of the generative cells.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00714555
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  • 6
    Electronic Resource
    Electronic Resource
    The formation of the generative cell in Polystachia pubescens (Orchidaceae) (1992)
    Springer
    Sexual plant reproduction 5 (1992), S. 131-137 
    Details
    ISSN: 1432-2145
    Keywords: Pollen grain ; Generative cell ; Formation and detachment ; Ultrastructure ; Polystachia pubescens ; Orchidaceae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The formation and nature of the generative cell wall and the detachment mode of the generative cell from the intine in Polystachia pubescens were observed by LM and TEM. Vesicles evenly positioned within the phragmoplast fuse to form a cell plate that divides the microspore into the generative and vegetative cell. This cell plate consists of callose. Before the generative cell leaves the intine, however, the callose is completely resorbed and is not replaced by any other substance. The generative cell becomes detached from the intine by moving towards the centre of the pollen grain. A constriction formed thereby gives the generative cell a bulb-like appearance and leads ultimately to the generative cell being pinched off. Plasma-filled vesicles originating from the generative cell remain between the intine and the plasma membrane of the vegetative cell.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00194872
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  • 7
    Electronic Resource
    Electronic Resource
    Electron microscopic examination of sporulation-deficient mutants of the fission yeast Schizosaccharomyces pombe (1992)
    Springer
    Archives of microbiology 158 (1992), S. 249-255 
    Details
    ISSN: 1432-072X
    Keywords: Sporulation ; Meiosis ; Ultrastructure ; Spindle pole body ; Spo mutants ; Schizosaccharomyces pombe ; Fission yeast
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A homothallic haploid strain of the fission yeast Schizosaccharomyces pombe initiates sexual reproduction (mating, meiosis and sporulation) in nitrogen-free sporulation medium. Cellular fine structures of eleven sporulation-deficient mutants (spo2, spo3, spo4, spo5, spo6, spo13, spo14, spo15, spo18, spo19 and spo20) of S. pombe in sporulation medium were examined by serial section-electron microscopy. The striking features of these spo mutants were: 1) the disappearance of the spindle pole bodies (SPBs) after the second meiotic division, and 2) the accumulation of unorganized structures. Based on histochemical staining, these structures were presumably unorganized spore wall precursors. In some mutants (spo3, spo5, spo6, spo19 and spo20), diploid zygotes contained four spore-like bodies which had walls similar to complete spore walls but failed to enclose any nuclei. After completion of the second meiotic division the nuclei were abnormally distributed in zygotic diploid cells. In the spo5, spo13, spo14, spo15 and spo19 mutants, the nuclei remained attached to each other. In spo5 and spo19, the inner membrane of the nuclear envelope was separated, but its outer membrane was shared by two sister nuclei. These observations suggest that the spo+ gene products play important roles in spatial and temporal organization of cellular structures during ascospore development.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00245240
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  • 8
    Electronic Resource
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    Frequency and structure of spinae on Chlorobium spp. (1992)
    Springer
    Archives of microbiology 157 (1992), S. 319-322 
    Details
    ISSN: 1432-072X
    Keywords: Chlorobiaceae ; Spinae ; Chlorobium ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Several Chlorobium species have been observed to possess spinae. Spinae are non-prosthecate, helically wound, rigid structures that extend from the outer bacterial cell surface into the external environment. Spinae length was variable within and between Chlorobium species. Spinae width was fairly consistent within species but varied between species (39.4 ± 2.6 nm to 82.6 ± 8.0 nm). The number of spinae per cell varied. The spinae did not penetrate the bacterial cell envelope and were randomly located on the cell surface. Spinae were not geographically restricted. The observation of spinae on pure cultures of Chlorobium spp. maintained for 25–30 years suggests that spinae may be of significant use to the cell.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00248675
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  • 9
    Electronic Resource
    Electronic Resource
    Ultrastructural investigations of Arbutus unedo-Laccaria amethystea mycorrhiza synthesized in vitro (1992)
    Springer
    Trees 7 (1992), S. 40-47 
    Details
    ISSN: 1432-2285
    Keywords: Arbutus unedo ; Laccaria amethystea ; Mycorrhiza ; Synthesis ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Anatomy and ultrastructure of the arbutoid mycorrhiza of Arbutus unedo-Laccaria amethystea from axenic culture are described. In comparison to non-inoculated roots, the rhizodermal cells of mycorrhizas are of greater volume, their nuclei are enlarged and show an irregular shape, plasmalemma and cytoplasm with mitochondria, plastids, endoplasmic reticulum and dictyosomes are increased. Several ontogenetical states are documented. The arbutoid mycorrhiza as a connecting link between ectomycorrhiza and ericoid mycorrhiza is discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00225230
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  • 10
    Electronic Resource
    Electronic Resource
    Immunocytochemical and electron-microscopic study of the elasmobranch nucleus sacci vasculosi (1992)
    Springer
    Cell & tissue research 270 (1992), S. 395-404 
    Details
    ISSN: 1432-0878
    Keywords: Nucleus sacci vasculosi ; Ultrastructure ; Immunocytochemistry ; Hypothalamus ; Tuberculum posterius ; Scyliorhinus caniculus, Raja undulata (Elasmobranchii)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The elasmobranch nucleus sacci vasculosi was studied by means of electron microscopy (in the dogfish) and immunocytochemistry (in the dogfish and the skate) by using antibodies against tyrosine hydroxylase, alpha-melanocyte-stimulating hormone, somatostatin, serotonin, and substance P. Ultrastructural study of the dogfish nucleus sacci vasculosi shows the presence of medium-sized cells that possess numerous mitochondria but that have no dense-core vesicles in the cytoplasm or in cell processes. Fibres of the conspicuous tractus sacci vasculosi have a beaded appearance and form conventional synapses with dendrites and cell perikarya of the nucleus sacci vasculosi. The perikarya of this hypothalamic nucleus were not immunoreactive to any of the antibodies tested, and fibres immunopositive to tyrosine hydroxylase, alpha-melanocyte-stimulating hormone, somatostatin, serotonin, and substance P were scarce within this nucleus, in both the dogfish and the skate. Dorsal to the nucleus sacci vasculosi, there are numerous positive neuronal processes in addition to many small neurons that show immunoreactivity to alpha-melanocyte-stimulating hormone, somatostatin and tyrosine hydroxylase. Two types of neuron occur in this dorsal region, displaying dense-core vesicles of either 100–160 nm or 60–100 nm diameter in their cytoplasm; they were identified as peptide-containing and monoamine-containing neurons, respectively. The neuropil of this region has a significantly different ultrastructure from that of the nucleus sacci vasculosi, with many processes containing dense-core vesicles. This group of neurons, located dorsal to the nucleus sacci vasculosi and showing (a) immunoreactivity to neuropeptides or to monoamine-synthesizing enzyme, and (b) cytoplasm with dense-core vesicles, was considered not to be a part of the nucleus sacci vasculosi but rather part of the nucleus tuberculi posterioris. These results support the non-peptidergic and non-aminergic character of the nucleus sacci vasculosi.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00328023
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  • 11
    Electronic Resource
    Electronic Resource
    Culture and characterization of dental follicle cells from rat molars (1992)
    Springer
    Cell & tissue research 267 (1992), S. 483-492 
    Details
    ISSN: 1432-0878
    Keywords: Dental follicle ; Cell culture ; Fibroblasts ; Immunocytochemistry ; Ultrastructure ; Collagen ; Gel-electrophoresis ; Western blotting ; Rat (Sprague-Dawley)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Because the dental follicle is necessary for the eruption of teeth of limited eruption, it was the objective of this study to determine if the cells of the follicle could be cultured in vitro. To achieve this, dental follicles and associated enamel organs were dissected from the first and second mandibular molars of 6–7-day-old rats (secretory stage of amelogenesis), and then cultured in a medium that promotes fibroblast growth — the predominant cell type of the dental follicle. The cultured cells grew to confluency and were kept through 3 passages before experimentation. The cultured cells were fibroblastic in shape, elongate with processes, and transmission electron microscopy revealed that they contained an abundant rough endoplasmic reticulum, but did not form desmosomes. Immunofluorescent staining for anti-vimentin showed that all the cells stained and electron-microscopic immunogold labeling indicated that the antibody was associated with intermediate filaments. As revealed by SDS-polyacrylamide gel electrophoresis and Western blotting, the cultured cells synthesized and secreted the extracellular matrix molecules fibronectin and procollagens. Subsequent immunofluorescence staining of permeabilized and non-permeabilized cells confirmed the presence of fibronectin and type I collagen both intra- and extracellularly. Thus, based on all the above characteristics, the cultured cells appeared to be fibroblasts derived from the dental follicle, although a few of the fibroblasts may be derived from undifferentiated mesenchymal cells interposed between the alveolar bone and follicle. Experiments now can be conducted to determine how these cultured cells respond directly to growth factors that alter the rates of tooth eruption.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00319370
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  • 12
    Electronic Resource
    Electronic Resource
    Structural organization of two fast, rhythmically active crustacean muscles (1992)
    Springer
    Cell & tissue research 267 (1992), S. 571-582 
    Details
    ISSN: 1432-0878
    Keywords: Crustacean muscle ; Ultrastructure ; Dye coupling ; Flagellum ; Scaphognathite ; Fascicles ; Mitochondria ; Carcinus maenas (Crustacea)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The organization of the flagellum abductor muscle and of a scaphognathite levator muscle of the green crab, Carcinus maenas, has been compared quantitatively using light and electron microscopy. These muscles are rhythmically active at relatively high frequencies and for long durations. Fibers of both muscles are interconnected to form fascicles of 50 or more fibers within which there is cytoplasmic continuity. A single muscle is made up of 8–12 fascicles. Individual fibers consist of a peripheral rind of densely packed mitochondria, a thick region of glycogen granules, and myofibrils arranged into scattered central islands. Less than half the volume-density of these muscles is contractile material, the balance being largely mitochondria and glycogen. The fibers within a muscle are structurally similar. They have short sarcomeres (about 2 μm), thin to thick filament ratios of about 3:1, and junctions between the sarcoplasmic reticulum and the transverse tubules at the M line. Sarcoplasmic reticulum occupies about 10% of the myofibrillar volume-density. A well developed sarcoplasmic reticulum appears to underlie the capacities of these two muscles for high frequency contraction; extensive mitochondria and glycogen stores should confer fatigue resistance under both aerobic and anaerobic conditions.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00319380
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  • 13
    Electronic Resource
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    Bethanechol and a G-protein activator, NaF/AlCl3, induce secretory response in Paneth cells of mouse intestine (1992)
    Springer
    Cell & tissue research 269 (1992), S. 213-220 
    Details
    ISSN: 1432-0878
    Keywords: Paneth cells ; Ultrastructure ; Morphometry ; Bethanechol ; Fluoride ion ; G-protein ; Mouse (Balb/c)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Paneth cells located at the bottom of intestinal crypts may play a role in controlling the bacterial milieu of the intestine. Using morphometry to clarify the secretory mechanism of the Paneth cells, we studied the ultrastructural changes in mouse Paneth cells produced following intra-arterial perfusion with Hanks' balanced salt solution containing a cholinergic muscarinic secretagogue (bethanechol), a neuroblocking agent (tetrodotoxin), or a G-protein activator (NAF/AlCl3). Bethanechol (2×10-4 mol/l) induced Paneth-cell secretion. Many Paneth cells massively exocytosed their secretory material into the crypt lumen; the enhanced secretion caused degranulation and vacuole formation. However, tetrodotoxin (2×10-6 mol/l) did not prevent the bethanechol-enhanced secretion by the Paneth cells. NaF (1×10-2 mol/l) and AlCl3 (1×10-5 mol/l) induced massive exocytosis of the Paneth cells; the exocytotic figures were similar to those observed in mice stimulated by bethanechol. G-protein activation was followed by a sequence of intracellular events, resulting in exocytosis.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00319611
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  • 14
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    Ultrastructural changes in primordial germ cells during early gonadal development of the common carp (Cyprinus carpio L., teleostei) (1992)
    Springer
    Cell & tissue research 267 (1992), S. 337-346 
    Details
    ISSN: 1432-0878
    Keywords: Primordial germ cell ; Ultrastructure ; Gonadal differentiation ; Cyprinus carpio (Teleostei)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A description is given of primordial germ cell (PGC) differentiation and gonadal development in carp from hatching until the age of 6 weeks. This period was chosen as the PGCs are mitotically silent before they start to proliferate rapidly after week 6. The PGCs increased in size between week 2 and week 4 after fertilization. Ultrastructurally, the perinuclear dense bodies present in PGCs from hatching onwards increased in size and formed the ‘cement’ between mitochondria. Moreover, from week 2 onwards, an elaborate Golgiapparatus was present in PGCs, indicating synthetic activity that may be related to PGC enlargement. During the observation period, gonadal tissue was gradually formed around the PGCs. From the age of 4 and 5 weeks onwards, two somatic cell types could be distinguished; the central type had a light appearance and was closely associated with the PGCs, the other type being darker and forming the peripheral layer of the developing gonads. Thus, during the period of mitotic quiescence, the PGCs and the gonads actively differentiate in preparation for the fast PGC proliferation that occurs after 6 weeks.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00302972
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  • 15
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    Ultrastructural study of the retinal pigment epithelium during metamorphosis in the sea lamprey (Petromyzon marinus L.) (1992)
    Springer
    Cell & tissue research 267 (1992), S. 375-384 
    Details
    ISSN: 1432-0878
    Keywords: Retinal pigment epithelium ; Ultrastructure ; Organelle differentiation ; Metamorphosis ; Lamprey, Petromyzon marinus (Cyclostomata)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The sequence of morphological changes in the retinal pigment epithelium during the metamorphic period of the sea lamprey Petromyzon marinus L. has been investigated using electron microscopy. At early metamorphic stages (stages I and II), photoreceptors are present in a small zone of the retina. During these stages, the lateral surface of the epithelial cells shows zonulae occludentes and adhaerentes. The degree of cell differentiation varies throughout the retinal pigment epithelium. Cells covering the differentiated photoreceptors in the central retina have phagosomes, whereas pigment granules appear only in the retinal pigment epithelium dorsal to the optic nerve head. Most epithelial cells have myeloid bodies; their morphology is more complex around the optic nerve head. At stage III, when photoreceptors develop over the whole retina, the distribution of cytoplasmic organelles is almost homogeneous in the retinal pigment epithelium. Subsequently, the basal plasma membrane of the epithelial cells becomes progressively folded and their apical processes enlarged. In addition, extensive gap junctions develop between retinal pigment cells. In late metamorphic stages, noticeable growth of myeloid bodies occurs and consequently the retinal pigment epithelium resembles that of the adult. This study also describes, for the first time, the presence of wandering phagocytes in the retinal pigment epithelium of lampreys; their role in melanosome degradation is discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00302976
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  • 16
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    In-vitro effects of angiotensin II on steroid production by hamster ovarian follicles and on ultrastructure of the theca interna (1992)
    Springer
    Cell & tissue research 268 (1992), S. 191-196 
    Details
    ISSN: 1432-0878
    Keywords: Angiotensin II ; Ovarian follicles ; Theca interna ; Ultrastructure ; Steroidogenesis ; Atresia ; Golden hamster (Rodentia)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Angiotensin II (AII) is present in the mammalian ovary and has been correlated with atresia in follicles. Since the theca interna may be one site at which atresia is intiated, we wished to determine whether AII exerts an effect on theca interna from explanted ovarian follicles of hamsters. Hamsters were sacrified on the morning of proestrus, and ovaries were removed. Preovulatory follicles were excised from the ovaries, and cultured with one of the following components: medium alone (control); medium plus AII (1x10-6 M); the AII-receptor antagonist [Sar1, Ile8] AII (1x10-4 M); or AII plus antagonist. After 72 h, the follicles were processed for transmission electron microscopy (to determine quantities of theca interna organelles involved in the steroid synthetic pathway) or for protein determination (to normalize steroid production rates). The incubation medium was drawn off and analyzed by radioimmunoassay for progesterone, androstenedione, or estradiol-17β. There was a significant positive correlation (r=0.92, P〈0.01) between follicular androstenedione secretion and area comprising theca interna smooth endoplasmic reticulum. In the theca interna, AII induced a two-fold and 1.6-fold increase in lipid droplet number and area comprising smooth endoplasmic reticulum, respectively (P〈0.05). Excess antagonist negated the increase in cell or-ganelles and also reduced androstenedione secretion compared with AII alone (P〈0.05). Most importantly, AII significantly augmented the ratio of androstenedione: estradiol-17β secretion by 44% over that of control. The ultrastructural changes observed in this study and the increase in the andostenedione: estradiol-17β production ratio are consistent with atresia-like changes in ovarian follicles. We believe, therefore, that AII is involved, possibly at its membrane receptor, in an aspect of the overall process of follicular atresia, operating in part at the level of the theca interna.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00338068
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  • 17
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    Ultrastructure of the basement membrane and its precursor in developing rat submandibular gland as shown by alcian blue staining (1992)
    Springer
    Cell & tissue research 268 (1992), S. 233-238 
    Details
    ISSN: 1432-0878
    Keywords: Alcian blue ; Basement membrane ; Lamina densa ; Meshwork ; Submandibular gland ; Ultrastructure ; Rat (Wistar-Imamichi)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The ultrastructure of the epithelial basement membrane and membrane precursor was studied in rat submandibular rudiment and a model system of the reconstructed basement membrane, by transmission electron microscopy following alcian blue staining. Directly beneath the epithelial plasma membrane, a meshwork layer was found to consist of anastomosing thin fibers arranged as a three-dimensional meshwork (100–400 nm in thickness). Straight strands (5–10 nm in diameter) could sometimes be seen to pass through the meshwork. Adjacent to this layer, a coarse network composed of threads (20–40 nm in diameter) connected the meshwork layer with collagen fibers of the underlying connective tissue. The earliest precursors recognized in the reconstruction-model system were part of the fine-meshwork structure, and showed this structure to be a fundamental component of the basement membrane.
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    URL: http://dx.doi.org/10.1007/BF00318791
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    Immunogold labelling of the cytoplasmic estradiol receptor in resting porcine endometrium (1992)
    Springer
    Cell & tissue research 270 (1992), S. 1-6 
    Details
    ISSN: 1432-0878
    Keywords: Estradiol receptor ; Endometrium ; Ovariectomy ; Immunohistochemistry ; Ultrastructure ; Pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Serial sections of resting porcine endometrium were analyzed with the monoclonal antibody 13H2 using goat antimouse IgG/5 nm gold as secondary reagent or with either polyclonal antibodies from goat #402 or the rat monoclonal antibody H222, both in combination with protein G/12 nm gold. A modestly higher labelling of nuclei than of cytoplasm was seen only with the monoclonal antibody H222. Polyclonal #402 and monoclonal 13H2 showed fewer attachments over nuclear than over cytoplasmic areas. The highest densities of attachment and of predominantly cytoplasmic labelling were obtained with the monoclonal antibody 13H2. The results confirm the earlier assumption of a restricted accessiblity of estradiol receptor in the cytoplasm of resting cells for immunoreagents.
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    URL: http://dx.doi.org/10.1007/BF00381873
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  • 19
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    Electron microscopical studies ofThorea ramosissima (Thoreaceae, Rhodophyta): Taxonomic implications ofThorea pit plug ultrastructure (1992)
    Springer
    Plant systematics and evolution 181 (1992), S. 233-244 
    Details
    ISSN: 1615-6110
    Keywords: Algae ; Rhodophyta ; Thorea ramosissima ; T. riekei ; Ultrastructure ; pit plugs as a taxonomic character
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The thallus ofThorea ramosissima was studied electron microscopically. The cells of the medulla, the cortex and the assimilatory hairs differ not only in size and number of plastids and their equipment with thylakoids but also in cell wall structure, the number of mitochondria and the activity of the Golgi apparatus, with dictyosomes transforming complete cisternae into Golgi vesicles with mucilaginous contents in the outer region of the cortex. The pit connections have plugs with a distinct plate—like (not dome-like) outer cap layer. BecauseT. riekei was reported to have dome-like outer cap layers and because this character was the main reason to place theThoreaceae into theBatrachospermales (Pueschel & Cole 1982),T. riekei was reinvestigated, too. A distinct outer cap could not be detected. The reliability of pit plug structure as a taxonomic character and the taxonomic position ofThorea is discussed.
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    URL: http://dx.doi.org/10.1007/BF00937447
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  • 20
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    Biochemical and immunological characterization of intermicrotubular cement in the feeding apparatus of phagotrophic eugienoids:Entosiphon, Peranema, andPloeotia (1992)
    Springer
    Protoplasma 168 (1992), S. 113-124 
    Details
    ISSN: 1615-6102
    Keywords: Cytoskeleton ; Phagotrophic ; Eugienoids ; Immunochemistry ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A monoclonal antibody (IIID12) obtained from mice immunized against the entireEntosiphon cytoskeleton highlights the feeding apparatus ofEntosiphon, Peranema, andPloeotia by IF. IGS at the ultrastructural level shows that it labels the cementing material surrounding the microtubular bundles in the three species studied. InEntosiphon additional structures, such as the supplementary plaque, the scaffold structure and the lenticular structure or canal thickening, are also detected by the antibody. Immunoblotting analysis after SDS-PAGE reveals a positive reaction with this antibody to the 58 and 66kDa protein bands inEntosiphon, 82 and 84kDa inPeranema, and 56 and 60kDa inPloeotia. These results demonstrate biochemical homologies in the proteins of the cement material in the three heteronematal eugienoids studied. The possible role of these proteins in microtubule assembly and stabilization is discussed, as well as the role of the cementing material in the mode of the feeding apparatus motion during the ingestion of food.
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    URL: http://dx.doi.org/10.1007/BF01666257
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  • 21
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    Ultrastructural characterization of somatic embryos regenerated from NaCl selected and nonselected calli ofDactylis glomerata (1992)
    Springer
    Protoplasma 170 (1992), S. 177-185 
    Details
    ISSN: 1615-6102
    Keywords: Dactylis glomerata L. ; Orchardgrass ; Sodium chloride tolerance ; Somatic embryo ; Tissue culture ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Calli were induced from leaf expiants of aDactylis glomerata L. (orchardgrass) genotype which has a high capacity for somatic embryogenesis. After 7 months culture on SH medium containing NaCl, a line was selected which was tolerant to 200 mM NaCl. When both selected and nonselected calli were maintained for 56 days on media containing 0 to 300 mM NaCl, the selected line showed significantly higher regeneration capacity than nonselected calli when placed on media containing more than 50 mM NaCl. Ultrastructural features of control somatic embryos not exposed to the salt were compared to those from nonselected and selected embryos cultured on 200 mM NaCl medium. In the presence of NaCl there were changes in the appearance of cell walls and mitochondria, accumulation of lipids and a higher degree of vacuolation in cells of nonselected embryos compared to control and selected embryos.
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    URL: http://dx.doi.org/10.1007/BF01378792
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  • 22
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    Immunocytochemical localization of callose in root cortical cells parasitized by the ring nematodeCriconemella xenoplax (1992)
    Springer
    Protoplasma 171 (1992), S. 1-6 
    Details
    ISSN: 1615-6102
    Keywords: (1→3)-β-Glucose ; Callose ; Cell wall ; Host-parasite interface ; Immunocytochemical ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Polyclonal antibodies specific to (1→3)-β-glucose were used to localize callose around stylets ofCriconemella xenoplax in parasitized cortical cells in root explants of carnation, crimson clover, and tomato. The nematode's stylet was inserted 5–6 μm through the wall of the parasitized cell without piercing the plasma membrane, which became invaginated around the stylet tip. A layer of electron-transparent callose was localized by immunogold labelling between the invaginated plasma membrane and the inserted stylet, except at the stylet orifice. The callose was continuous with the inner surface of the wall of the parasitized cell around the site where the stylet penetrated. When the parasitized cell was located in the second layer of the cortex, the nematode's stylet first passed through a subepidermal cortical cell. The integrity of the plasma membrane of the transected cell was maintained and callose was deposited around the portion of the nematode's stylet that traversed the cell. We suggest that callose deposition around nematode stylets in parasitized cells is a common wound response elicited when plant-parasitic nematodes feed from cells.
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    URL: http://dx.doi.org/10.1007/BF01379274
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  • 23
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    Rose leaf structure in relation to different stages of micropropagation (1992)
    Springer
    Protoplasma 166 (1992), S. 165-176 
    Details
    ISSN: 1615-6102
    Keywords: Cuticle ; Humidity ; Leaf structure ; Micropropagation ; Rosa ; Stomata ; Ultrastructure ; Wax
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The Mme Isaac Pereire rose was investigated in an attempt to establish how micropropagated roses might best be weaned into normal growth conditions. Leaves of in vitro grown plants, weaned plants and the stock plant were studied, using light microscopy and different scanning and transmission electron microscopical techniques. Features that varied in the different growing conditions were leaf size and thickness, amount of wax, thickness of cuticle and external epidermal cell wall, number and aperture of the stomata, size of the epidermal cells, number of layers of the palisade cells, and size of the chloroplasts in the mesophyll. The rose in the present study had wax on the in vitro cultured plants; this wax was of similar ultrastructural appearance to that of the stock plant, even though in smaller quantities. Weaned plants had an intermediate amount of wax. The cuticle was thin, ranging from 0.04 μm on plants growing in vitro to 0.3-0.6 μm on weaned plants and stock plants. Stomata were always wide-open on leaves taken from cultures with a relative humidity of 100%. After four weeks in a humidity lowered to 85% stomata had closed.
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    URL: http://dx.doi.org/10.1007/BF01322779
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    Ultrastructure of cuticular exudations in parasitic juvenileHeterodera schachtii, as related to cuticle structure (1992)
    Springer
    Protoplasma 166 (1992), S. 67-77 
    Details
    ISSN: 1615-6102
    Keywords: Cuticle ; Cuticular exudations ; Exudations ; Heterodera schachtii ; Ultrastructure ; Host-parasite interactions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The development ofHeterodera schachtii inside roots of a cruciferous host plant grown under monoxenic conditions in an agar medium was observed with video-enhanced contrast light microscopy. One to 6 days after inoculation, roots were excised and processed for electron microscopic observations. Exudates were present on the cuticle surfaces of J 2 and early J 3 juveniles located at feeding sites. Fibrillar exudations were correlated with similar fibrillar patterns in the epicuticle, exocuticle, intermediate zone, and the striated endocuticle. Secretion vesicles assembled at many Golgi sites in the hypodermis, appeared to coalesce and form large electron translucent vesicles in the cytoplasm. We propose that secretion vesicles migrate toward the cuticle, contact the plasmalemma and transfer their contents by exocytosis or a similar mechanism to a secretion accumulation site. These contents are associated with cuticle structure and emerge as surface exudations.
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    URL: http://dx.doi.org/10.1007/BF01320145
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    Morphogenesis of the feeding apparatus ofEntosiphon sulcatum (1992)
    Springer
    Protoplasma 168 (1992), S. 125-135 
    Details
    ISSN: 1615-6102
    Keywords: Morphogenesis ; Phagotrophic ; Euglenoids ; Immunocytochemistry ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The disruption and development of the siphon during division ofEntosiphon have been followed by immunofluoresence with both an anti-cement MAb (IIID12) and an anti-tubulin MAb. (IVA10), by nuclear DNA labelling and by electron microscopy of serial section. The disruption of the parental siphon begins at the reservoir level where two new transversely orientated daughter siphons arise. In the degenerating bundles the cement disappears, first liberating the microtubules which then depolymerize. The first structure which surrounds the anterior part of the two young siphons is a loop of 5 microtubules linked to the reservoir membrane. From around this loop a row of perpendicular microtubules sink in the cytosplasm; they will form the primary row of microtubules in the definitive bundles. Inside the loop, reinforced microtubules are seen beneath the membrane, they will generate the future vanes, and also penetrate into the cytosplasm. Amorphous material surrounds the young siphons and may correspond to cement material. The growth of the siphons proceeds as they adopt a central longitudinal position in the cell. The cement material progressively condenses on structures such as the primary row of microtubules. The bundles, the supplementary plaque, and the scaffold. After flagellar partition each of the canals becomes distinct and cytokinesis occurs from the anterior end. These observations indicate that the microtubular loop could be the source of microtubule-organizing centre (MTOC) proteins initiating the assembly of the primary row of microtubules. Bundle microtubules start to assemble at the anterior end and extend backwards. The microtubules of the loop could be linked to roots associated with the basal bodies which double in number before division. The cement later condenses, linking and stabilizing the structures. Microfibrils play an important role in basal body and siphon separation and positioning.
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    URL: http://dx.doi.org/10.1007/BF01666258
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  • 26
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    Ultrastructural changes in the cell wall, nucleus and cytoplasm of pollen mother cells during meiotic prophase I inLycopersicon esculentum (Mill.) (1992)
    Springer
    Protoplasma 169 (1992), S. 139-147 
    Details
    ISSN: 1615-6102
    Keywords: Cell wall ; Lycopersicon esculentum ; Microsporogenesis ; Pollen development ; Prophase I ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Throughout the premeiotic to late prophase I stages of meiosis in the anthers of tomato (Lycopersicon esculentum) extensive changes occurred in the ultrastructure of pollen mother cells (PMCs). During early prophase, the wall of each PMC developed a layered appearance and was broadened both by the widening of the middle lamella as well as by intensive deposition of microfibrils in the wall. By late prophase, however, the microfibrils adjacent to the plasmalemma dissipated. At the same time, callose was deposited between the wall and the plasmalemma. The nucleus of the PMCs also underwent changes. During early prophase, the nucleolus consisted of a linear series of three segments, with a separation of the granular and fibrillar portions. By late prophase, the nucleoli were less distinct as the nucleus was highly vacuolate. Mitochondria were initially simple with lightly stained matrix and few cristae but, during the course of prophase, they acquired a more densely-stained matrix with dilated cristae. Plastids remained relatively undifferentiated and, at late prophase, many were convoluted in appearance and constricted at intervals indicating their division. Cytoplasmic connections between adjacent PMCs were broad enough to permit the passage of organelles and were retained through to metaphase I. These cytological and wall changes appear to be a prerequisite for the subsequent development of microspores.
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    URL: http://dx.doi.org/10.1007/BF01323613
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    Ultrastructure of freeze-substituted pollen tubes ofLilium longiflorum (1992)
    Springer
    Protoplasma 167 (1992), S. 215-230 
    Details
    ISSN: 1615-6102
    Keywords: Lilium ; Freeze substitution ; Pollen tubes ; Rapid freeze fixation ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary In view of the importance of the lily pollen tube as an experimental model and the improvements in ultrastructural detail that can now be attained by the use of rapid freeze fixation and freeze substitution (RF-FS), we have reexamined the ultrastructure of these cells in material prepared by RF-FS. Several previously unreported details have been revealed: (1) the cytoplasm is organized into axial “slow” and “fast” lanes, each with a distinct structure; (2) long, straight microtubule (MT) and microfilament (MF) bundles occur in the cytoplasm of the fast lanes and are coaligned with every organelle present; (3) the cortical cytoplasm contains complexes of coaligned MTs, MFs, and endoplasmic reticulum (ER); (4) the cortical ER is arranged in a tight hexagonal pattern and individual elements are closely appressed to the plasma membrane with no space between; (5) mitochondria and ER extend into the extreme apex along the flanks of the pollen tube, and vesicles and ER are packed into an inverted cone-shaped area at the center of the apex; (6) MF bundles in the tip region are fewer, finer, and in random orientation in comparison to those of the fast lanes; (7) the generative cell (GC) cell wall complex contains patches of plasmodesmata; (8) The GC cytoplasm contains groups of spiny vesicles that are closely associated with and seem to be fusing with or pinching off from mitochondria, and (9) the vegetative nucleus (VN) contains internal MT-like structures as well as numerous cytoplasmic MTs associated with its membrane and also located between the VN and GC.
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    URL: http://dx.doi.org/10.1007/BF01403385
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    Changes in the lysosome structure during the formation of zoospores inTrebouxia potteri (1992)
    Springer
    Protoplasma 171 (1992), S. 19-27 
    Details
    ISSN: 1615-6102
    Keywords: Lysosome ; Morphogenesis ; Trebouxia potteri ; Ultrastructure ; Zoospore formation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Changes in the lysosome structures were examined by electron microscopy during the formation of zoospores inTrebouxia potteri. Lysosomes in vegetative cells were homogeneously filled with electron-dense material. At the beginning of zoospore formation, lysosomes invaginated or evaginated to take up mitochondria, ER, or cytoplasmic ground plasma. The ingested organelles became disorganized within the lysosomes. During this disruption of these organelles, the lysosomal contents became heterogeneous, suggesting a decrease in the amount of enzymes within the lysosomes. Golgi bodies and ER seemed to be involved with the disruption of the organelles, probably supplying some substances necessary for the functioning of the lysosomes. Amount of electron-dense materials decreased and, finally, only one to three small spherical aggregates remained in the lysosomes. Then the lysosomes appeared to shrink via loss of watery substances or cutting off of electron-transparent regions. After these changes in lysosome structure, nuclei started to divide successively for formation of the zoospores. The possibility is proposed that the drastic cytoplasmic changes operated by lysosomes trigger the following morphogenetic events in the formation of zoospores.
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    URL: http://dx.doi.org/10.1007/BF01379276
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  • 29
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    Cytometric and electron microscopic studies of the direct interaction of divalent nickel with intact and chemically modified HuT-78 lymphoblasts (1992)
    Springer
    Cell biology and toxicology 8 (1992), S. 27-41 
    Details
    ISSN: 1573-6822
    Keywords: Lymphoblasts ; Nickel ; Cytometry ; Ultrastructure ; Membrane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Cytometric and ultrastructural studies on 24 hr cultures of intact, 1.0 mM H5I06, and 0.1 mM SeO2-oxidized HuT-78 lymphoblasts were performed after their direct, 30 min interaction with 1.0 mM NiCl2. Except for moderately depressed cell viability, divalent nickel did not alter the progression of intact and oxidized target cells through the phases of the cell cycle. Although the plasma membrane remained structurally intact, marked distortion of mitochondria structure and increased osmiophilia were an invariable attribute of all nickel-pulsed cells. Moreover, numerous electron-opaque, intracellular depositions were detected in SeO2-oxidized, nickel-pulsed cells. It is concluded that the initial state of plasma membrane, and the interaction of nickel with other trace elements, have jointly determined the response of HuT-78 cells to brief and direct, divalent nickel pulses.
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    URL: http://dx.doi.org/10.1007/BF00119293
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