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  • 1
    ISSN: 1432-0878
    Keywords: Vascular smooth muscle ; Spontaneously hypertensive rat ; Reaggregate cultures ; Ultrastructure ; Collagen synthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Vascular smooth muscle cells were taken from the aortae of the WKY (normotensive) and SHR (spontaneously hypertensive) strains of rat by enzymatic dispersion and put into reaggregate culture. Initially the cells became individual spheroids having average diameters of 10 μm and surfaces that were either rough or smooth. The cells were far more complex than they appeared on their surfaces; after one day in culture, there was considerable internal variation in these cells. All the cells, whether WKY or SHR, lost the bulk of their cytoplasmic contents (including myofilaments, many mitochondria, and vesicular structures) in the early stages of culture and eventually became flattened. After 14 days in culture, these modified cells collected to form reaggregates that were commonly roughly spherical and several hundred μm in diameter. These reaggregates consisted of peripheral regions made up of several layers of flattened cells overlying cores formed by glia-like networks of cells similar in cytological appearance to the cells at the periphery. The meshes formed in this way contained cellular debris derived from dead cells or extrusion of cellular contents. It appears that SHR cells are quicker to form reaggregates than are WKY cells. Yet the SHR cells retained a rounded conformation after five days, whereas the WKY cells were more flattened and formed a more discrete aggregate at this stage of culture. However, by the fourteenth day of culture, differences between the two cell strains were not so pronounced, as far as could be judged by observations made with scanning and transmission electron microscopy. Both WKY and SHR cells at 14 days appeared highly secretory, possessing large Golgi systems as well as numerous ER cisternae and mitochondria. SHR cells produced greater amounts of connective tissue at all stages of culture than did WKY cells, indicating that a similar difference may contribute to the hypertension which develops naturally in situ in SHR animals.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 136 (1972), S. 227-245 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The stellate cell in the pars distalis of Anolis carolinensis has been studied with the electron microscope. This cell type is characterized by the lack of secretory granules, and it possesses elongate processes that insert between secretory cells. Few cytoplasmic filaments are present in these processes, and desmosomes linking them to adjacent stellate cells or to secretory cells are seen infrequently in control animals. Stellate cells are often encountered in the caudal half of the pars distalis, but they are less commonly found in the rostral half. In animals undergoing thyroidal depression, thyroidectomy cells arise in the caudal pars distalis. Concurrently, stellate cells of that region hypertrophy and exhibit increased numbers of desmosomes, complex intercellular junctions, and micropinocytotic vesicles. Injected horseradish peroxidase penetrates the intercellular spaces, enters the micropinocytotic vesicles, and is transported to the interior of the stellate cell. It is suggested that stellate cells in Anolis under certain conditions may transport materials between the bloodstream and secretory cells.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 143 (1974), S. 409-433 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Gonadotrophic cells in the pars distalis of Anolis carolinensis often contain juxtanuclear concentrations of filaments with diameters intermediate in size (approximately 100 Å) between microtubules and microfilaments. Their size and their substructure, which gives them a tubular appearance when they are displayed in cross-section, appear to place these filaments in the “intermediate filament” category (Ishikawa et al., '68). In their juxtanuclear position in the intact animal, the intermediate filaments are collected in randomly-oriented tangles. In castrated specimens of Anolis, gonadotrophs degranulate and elongate. During this elongation, increased numbers of microtubules appear in orientation parallel to the long axis of the cell, and the 100 Å filaments reassemble in rod-like masses oriented parallel to the microtubules. This apparent distributional interaction may facilitate the elongation of the cell. Intimate physical associations between the intermediate filaments and secretory granules suggest that the filaments may act in the movement of the granules during the processes of degranulation and secretion.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 1 (1984), S. 271-277 
    ISSN: 0741-0581
    Keywords: Vascular cell cultures ; Transmission electron microscopy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: A method is described for obtaining optimal, reproducible ultrastructure of vascular smooth muscle cells and vascular endothelial cells in culture. Routinely grown cultures are prepared for TEM with a precise regimen of fixation, postfixation, en bloc staining, dehydration, and embedment. The most important aspects of this procedure are the following: (1) fixation with a percentage-gradient series of glutaraldehyde solutions at 37°C, (2) immediate postfixation with osmium tetroxide solution, and (3) block-staining with uranyl acetate solution to eliminate any extraction of constituents during subsequent processing.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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