Literature DB >> 7237525

Electron-microscopic studies on reaggregate cultures of vascular smooth muscle cells from normotensive and spontaneously hypertensive rats.

S Yoneda, M S Forbes, E Zelcer, N Sperelakis.   

Abstract

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 micrometers 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 micrometers 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.

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Year:  1981        PMID: 7237525     DOI: 10.1007/bf00233577

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  35 in total

Review 1.  The smooth muscle cell in culture.

Authors:  J Chamley-Campbell; G R Campbell; R Ross
Journal:  Physiol Rev       Date:  1979-01       Impact factor: 37.312

2.  Development of a strain of spontaneously hypertensive rats.

Authors:  K OKAMOTO; K AOKI
Journal:  Jpn Circ J       Date:  1963-03

3.  Human vascular smooth muscle in culture. Growth and ultrastructure.

Authors:  M A Gimbrone; R S Cotran
Journal:  Lab Invest       Date:  1975-07       Impact factor: 5.662

4.  Evaluation and publication of scanning electron micrographs.

Authors:  J M Clark; S Glagov
Journal:  Science       Date:  1976-06-25       Impact factor: 47.728

5.  Electron microscopic observations on the formation of elastic fibers in primary cultures of aortic smooth muscle cells.

Authors:  A Hinek; J Thyberg
Journal:  J Ultrastruct Res       Date:  1977-07

Review 6.  Structural diversity of gap junctions. A review.

Authors:  W J Larsen
Journal:  Tissue Cell       Date:  1977       Impact factor: 2.466

7.  Fine surface structure of heart cells in culture--in comparison with the changes in heart cells due to changes of the substratum, and L-cell.

Authors:  S Yoneda
Journal:  Jpn Circ J       Date:  1978-09

8.  Lipid accumulation in human aortic smooth muscle cell lysosomes.

Authors:  B Coltoff-Schiller; S Goldfischer; H Wolinsky; S M Factor
Journal:  Am J Pathol       Date:  1976-04       Impact factor: 4.307

Review 9.  Cultured heart cell reaggregate model for studying cardiac toxicology.

Authors:  N Sperelakis
Journal:  Environ Health Perspect       Date:  1978-10       Impact factor: 9.031

10.  Thick filaments in vascular smooth muscle.

Authors:  C E Devine; A P Somlyo
Journal:  J Cell Biol       Date:  1971-06       Impact factor: 10.539

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