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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 329-347 
    ISSN: 0886-1544
    Keywords: actin ; microfilaments ; heavy meromyosin ; mammary gland ; secretion ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Cytochalasin B, a microfilament-altering drug, inhibits lactose synthesis in lactating guinea pig mammary gland [Biochim. Biophys. Acta 392:20, 1975] but not primarily by inhibiting glucose transport [Eur. J. Cell Biol. 20:150, 1979]. In order to study the possible role of microfilaments in lactose synthesis and secretion, we isolated both the alveolar (milk-secreting) and myoepithelial (contractile) cells from lactating mammary gland. Light microscopy shows that the alveolar cell fraction (viability approximately 71%) is homogenous and that the cells retain strong polarity of secretory structures in the apical region. Two proteins were extracted from the alveolar cell fraction. One (mol wt 42,000) comigrates with skeletal muscle actin on SDS-PAGE gels. The other, a high-molecular-weight (180,000) protein (HMWP) may be analogous to actin-binding protein or clathrin. An extract from the myoepithelial cell fraction also contains a protein that comigrates with actin but no HMWP. Whole tissue extract contains the 42K protein, and a 185K HMWP. Examination of the alveolar cell extract by electron microscopic (EM) negative staining revealed meshworks of multistranded, interconnecting filaments, with attached globular structures (100-200 A) (possibly the HMWP) and single filaments (40-60 A diameter) branching off. To localize these filamentous structures in situ, whole tissue was glycerinated and incubated with rabbit skeletal muscle heavy meromyosin (HMM). Masses of filaments in myoepithelial cells served as convenient standards for HMM decoration. Decorated filaments have cross-arms or projections, unlike the narrow, smooth filaments of control tissue. Decorated filaments in alveolar cells are located beneath the plasma membrane, in close association with secretory vacuoles, and near the Golgi apparatus; filaments near the latter two are often oriented perpendicular to the plasma membrane. Microvesicles are embedded in meshworks under the plasmalemma and near the Golgi apparatus. Intermediate-sized (85-115 A diameter), non-decorated filaments diverge from the meshworks of decorated filaments. Microvesicles are associated with intermediate-sized filaments as well. The association of actin-like filaments with secretory vacuoles and microvesicles and their location in areas of the cell concerned with biosynthetic activities suggest a possible function in the intracellular transport of secretory products.
    Additional Material: 13 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 113 (1971), S. 420-440 
    ISSN: 1432-0878
    Keywords: Crayfish ; Hepatopancreas ; Cell differentiation ; Digestion ; Fine structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The ultrastructure of R-, F-, and B-cells and of the myoepithelial network in crayfish hepatopancreas tubules was studied as a basis for the functional interpretation of hepatopancreatic digestive activity: 1. R-cells absorb luminal nutrients, mainly via contact digestion and molecular transport, and they store and metabolize glycogen and lipids. To this extent, R-cells combine the functions of vertebrate intestinal absorptive and hepatic parenchymal cells. 2. F-cells synthesize digestive enzymes and sequester them in a supranuclear vacuole which enlarges by pinocytic intake of luminal nutrients and fluids. 3. F-cell to B-cell transformation results from continued engorgement of the F-cell's supranuclear vacuole until only the nuclear region and a pinocytically activeapical complex remain identifiable. 4. B-cell secretion involves pinching off of the apical complex followed by extrusion of the enzyme-rich vacuolar contents. 5. The tubule's myoepithelial network consists of circular fibers, each containing a single myofibril, which branch to form longitudinal fibers. Sarcomeres are long (10–12 μ) and each thick myofilament is surrounded by 11–13 thin ones. This arrangement permits coordinated, tonic contractions of tubule segments which transport nutrients “in” and enzymes “out”. 6. Neurosecretory control of tubular function is suggested by the presence of vesicle-containing, extratubular cell processes which contact the circular muscle fibers.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 142 (1974), S. 241-263 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Regions of the crayfish kidney were examined by electron microscopy. Coelsmosac cells are loosely bound together by desmosome-like spot junctions, and connected to the basal lamina via characteristic pedicels. The cytoplasm contains numerous vesicles and vacuoles of various sizes and is often crowded with large, lysosome-like granules or dense bodies. The morphology suggests a filtration mechanism with reabsorption of materials such as protein from the filtrate and secretion of other substances into the lumen.The labyrinth is composed of cuboidal to columnar cells which possess a brush border, long and narrow intercellular spaces, basal plasmalemmal invaginations and typical cytoplasmic components. Two sub-regions are distinguishable. The morphology of labyrinth I suggests that these cells move fluid isotonically across the epithelium. Labyrinth II, in addition to isotonic transport, appears to be more active in the endocytic uptake and intracellular digestion of large molecules such as protein.The nephridial canal consists of cells which lack a brush border, but display extensive basal invaginations associated with elongated mitochondria. A proximal and distal region are cytologically distinguishable. Proximally, the cells are small and filled with mitochondria throughout. Scattered within the cytoplasm are vesicles, vacuoles, diffuse glycogen, free ribosomes, dense bodies and some rough endoplasmic reticulum. Distally, the cells are less compact, larger, and cuboidal to columnar in shape. The cytoplasm is similar to that of the proximal cells, but the basal invaginations are even larger and more extensive. The morphology of cells in both regions of the nephridial canal is highly suggestive of active solute reabsorption, probably occurring against an osmotic gradient.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 141 (1973), S. 133-145 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Cytological and cytochemical methods were used to identify and characterzie six distinct regions of the crayfish kidney: coelomosac, labyrinth I and II, and nephridial canal I, II, and III. Cells of the coelomosac possess cytoplasm which is strongly PAS-positive, but poor in RNA and protein. Their nuclei possess unusual projections which extend to the basal plasmalemma. Labyrinth I contains columnar cells rich in glycogen. Labyrinth II is characterized by a distended lumen and by shorter cells with high cytoplasmic RNA, many possessing a large intracellular vacuole. A PAS-positive brush border is unique to the two portions of the labyrinth. Cells in the nephridial canal show strong reactions for RNA and Mg++-dependent ATPase. In nephridial canal I and II, cells are flattened to cuboidal with the lumen being more distended in nephridial canal I than anywhere else in the tubule. In nephridial canal III, the cells are large and columnar, and the cytoplasmic RNA concentration is greatest apically. Nuclei in all regions of the tubule epithelium, except coelomosac, are large and react strongly for protein. Coelomosac nuclei and those in blood cells are condensed and contain little protein. The cytoplasm of blood cells displays a significant amount of RNA, and traces of polysaccharide material.These observations demonstrate the presence of highly specialized morphological and histochemical alterations along the length of the kidney tubule and indicate sequential modification of urine in the lumen. Evident morphological and cytochemical likenesses between analogous regions of the mammlian nephron and the crayfish kidney tubule suggest that basic physiological similarities may also exist.
    Additional Material: 2 Ill.
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  • 5
    Publication Date: 1971-01-01
    Print ISSN: 0302-766X
    Electronic ISSN: 1432-0878
    Topics: Biology , Medicine
    Published by Springer
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