Literature DB >> 11591176

Cell volume and rate of proliferation, but not protein expression pattern, distinguish pup/intimal smooth muscle cells from subcultured adult smooth muscle cells.

E McKilligin1, D J Grainger.   

Abstract

Smooth muscle cells from neonatal rats and from injured blood vessels grow with a characteristic cobblestone morphology that distinguishes them from adult smooth muscle cells. This has led to the proposition that there are two distinct types of smooth muscle cells with different proliferative capacity. Here we systematically compare the properties of subcultured adult smooth muscle cells in culture and clonal lines of cobblestone smooth muscle cells from both neonatal rats and injured vessels. The cobblestone smooth muscle cells have a significantly smaller average cell volume, estimated using two different flow cytometry measurements. However, the two types of smooth muscle cells have indistinguishable protein expression patterns when the levels of more than 20 different proteins (including cytoskeletal proteins, matrix proteins, cytokines, cytokine receptors, adhesion molecules and enzymes) are measured by quantitative immunofluorescence. Furthermore, in contrast to previous observations, we demonstrate that both types of smooth muscle cells secrete a powerful mitogenic activity. The higher cell density achieved by the cobblestone smooth muscle cells in culture was responsible for the earlier reports that this mitogenic activity was secreted only by cobblestone smooth muscle cells. We conclude that many of the differences seen between cobblestone smooth muscle cells and adult smooth muscle cells in vitro (proliferation rate, morphology, protein expression pattern, secretion of mitogenic activity) could be attributable to a stable difference in the median cell volume of the cultures.

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Year:  2001        PMID: 11591176      PMCID: PMC6495989          DOI: 10.1046/j.0960-7722.2001.00212.x

Source DB:  PubMed          Journal:  Cell Prolif        ISSN: 0960-7722            Impact factor:   6.831


  32 in total

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Authors:  S M Schwartz; L Foy; D F Bowen-Pope; R Ross
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Review 2.  The intima: development and monoclonal responses to injury.

Authors:  S M Schwartz; M W Majesky; C E Murry
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3.  Cytoskeletal features of rat aortic cells during development. An electron microscopic, immunohistochemical, and biochemical study.

Authors:  O Kocher; O Skalli; D Cerutti; F Gabbiani; G Gabbiani
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4.  Characterization of cloned aortic smooth muscle cells from young rats.

Authors:  J M Lemire; C W Covin; S White; C M Giachelli; S M Schwartz
Journal:  Am J Pathol       Date:  1994-05       Impact factor: 4.307

5.  Age influences the replicative activity and the differentiation features of cultured rat aortic smooth muscle cell populations and clones.

Authors:  M L Bochaton-Piallat; F Gabbiani; P Ropraz; G Gabbiani
Journal:  Arterioscler Thromb       Date:  1993-10

6.  Vimentin-containing smooth muscle cells in aortic intimal thickening after endothelial injury.

Authors:  G Gabbiani; E Rungger-Brändle; C de Chastonay; W W Franke
Journal:  Lab Invest       Date:  1982-09       Impact factor: 5.662

7.  Expression of transforming growth factor-beta 1 is increased in human vascular restenosis lesions.

Authors:  S Nikol; J M Isner; J G Pickering; M Kearney; G Leclerc; L Weir
Journal:  J Clin Invest       Date:  1992-10       Impact factor: 14.808

8.  The size control of fission yeast revisited.

Authors:  A Sveiczer; B Novak; J M Mitchison
Journal:  J Cell Sci       Date:  1996-12       Impact factor: 5.285

9.  Phenotype-dependent response of cultured aortic smooth muscle to serum mitogens.

Authors:  J H Chamley-Campbell; G R Campbell; R Ross
Journal:  J Cell Biol       Date:  1981-05       Impact factor: 10.539

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