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  • Artikel  (4)
  • Collagen synthesis  (1)
  • Embryonic development  (1)
  • Muscle ultrastructure  (1)
  • Vascular cell cultures  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Cell & tissue research 166 (1976), S. 83-90 
    ISSN: 1432-0878
    Schlagwort(e): Embryonic development ; Ventricular myocardium ; Transverse and axial tubules ; Guinea pig
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Summary Developing transverse (T) tubules are found in embryonic guinea pig ventricular myocardium after approximately eight weeks of gestation. By the time of birth (nine weeks total gestation), longitudinally-oriented axial tubules connected to the T tubules also have formed, and the majority of cells closely resemble those of the adult. The form taken by the developing T and axial tubules suggests that they are generated in a manner similar to that for T tubules in chick and rat skeletal muscle, namely by repeated formation of caveolae.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Cell & tissue research 134 (1972), S. 1-11 
    ISSN: 1432-0878
    Schlagwort(e): Muscle ultrastructure ; (Na+, K+)-ATPase localization ; Sarcotubules ; Sarcoplasmic reticulum ; Junctional SR
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Summary ATPase activity sensitive to ouabain was examined in both cardiac (ventricular) and skeletal (tibialis anterior) muscle cells of the mouse. Short-term fixation was combined with incubation in a medium designed to reduce artifactual deposition of lead phosphate. With incubation medium containing Na+ and K+, Pb3 (PO4)2 precipitate appears throughout the sarcoplasmic reticulum (SR) of both cardiac and skeletal cells. The precipitate generally is heavier in the junctional SR than in network SR, although the two regions are interconnected. Ouabain (1 mM) eliminates activity in the network SR of myocardial cells, but only reduces it in skeletal muscle cells. The total ATPase activity of junctional cisternae of the SR of myocardial cells does not appear to be reduced by ouabain, whereas the activity of the terminal cisternae of skeletal muscle is substantially diminished. The use of an incubation medium containing zero K+ reduces the level of activity, but not consistently. These data suggest that (Na+, K+)-ATPase is present in the network SR of both cardiac and skeletal muscle cells, and probably in the terminal cisternae of skeletal muscle cells.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    ISSN: 1432-0878
    Schlagwort(e): Vascular smooth muscle ; Spontaneously hypertensive rat ; Reaggregate cultures ; Ultrastructure ; Collagen synthesis
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: 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.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 1 (1984), S. 271-277 
    ISSN: 0741-0581
    Schlagwort(e): Vascular cell cultures ; Transmission electron microscopy ; Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Allgemeine Naturwissenschaft
    Notizen: 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.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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