Thromb Haemost 1996; 75(05): 854-858
DOI: 10.1055/s-0038-1650379
Original Article
Schattauer GmbH Stuttgart

Evidence for Cultured Human Vascular Smooth Muscle Cell Heterogeneity: Isolation of Clonal Cells and Study of their Growth Characteristics

Omar Benzakour
The Thrombosis Research Institute, Manresa Road, Chelsea, London, UK
,
Chryso Kanthou
The Thrombosis Research Institute, Manresa Road, Chelsea, London, UK
,
Sandip M Kanse
The Thrombosis Research Institute, Manresa Road, Chelsea, London, UK
,
Michael F Scully
The Thrombosis Research Institute, Manresa Road, Chelsea, London, UK
,
Vijay V Kakkar
The Thrombosis Research Institute, Manresa Road, Chelsea, London, UK
,
David N Cooper
The Thrombosis Research Institute, Manresa Road, Chelsea, London, UK
› Author Affiliations
Further Information

Publication History

Received 06 November 1995

Accepted after revision 19 January 1996

Publication Date:
10 July 2018 (online)

Summary

The monoclonal theory of atherosclerosis postulates that the initial vascular smooth muscle cell (VSMC) proliferative event involves the expansion of a single cell or a sub-population of cells thus implying differences in the replicative potential of VSMC. Using the technique of limited dilution, VSMC clones derived from animal tissues have been previously isolated and shown to be morphologically heterogeneous. However, the same technique applied to human VSMC (HVSMC) has been unsuccessful, possibly because HVSMC do not grow when plated at very low densities. In this report, the anchorage-independent growth of HVSMC in semi-solid medium was studied. Platelet-derived growth factor-BB (PDGF-BB) and to a lesser extent PDGF-AB and basic fibroblast growth factor (bFGF) induced colony formation. This assay provided a tool for the isolation of HVSMC clones. In terms of their growth characteristics and responsiveness to several growth factors, isolated HVSMC clones and the original parental cell population exhibited marked heterogeneity.

 
  • References

  • 1 Ross R. The pathogenesis of atherosclerosis: a perspective for the 1990s. Nature 1993; 362: 801-809
  • 2 Ross R, Glomset JA. The pathogenesis of atherosclerosis. N Engl J Med 1976; 295: 369-377
  • 3 Benditt EP, Benditt JM. Evidence for a monoclonal origin of human atherosclerotic plaques. Proc Natl Acad Sci USA 1973; 70: 1753-1756
  • 4 Orekhov AN, Andreeva ER, Krushinsky AV, Smirnov VN. Primary cultures of enzyme-isolated cells from normal and atherosclerotic human aorta. Med J 1984; 62: 255-259
  • 5 Bochaton-Piallat ML, Gabbiani F, Ropraz P, Gabbiani G. Cultured aortic smooth muscle cells from newborn and adult rats show distinct cytoskeletal features. Differentiation 1992; 49: 175-185
  • 6 Majesky MW, Giachelli CM, Reidy MA, Schwartz SM. Rat carotid neointimal SMC re-express a developmentally regulated mRNA phenotype during repair of arterial injury. Cell Regul Res 1992; 71: 759-768
  • 7 Weissberg PL, Grainger DJ, Shanahan CM, Metcalf JC. Approaches to the development of selective inhibitors of vascular smooth muscle cell proliferation. Cardiovasc Res 1993; 27: 1191-1198
  • 8 Bochaton-Piallat ML, Gabbiani F, Ropraz P, Gabbiani G. Age influences the replicative activity and the differentiation features of cultured rat aortic smooth muscle cell populations and clones. Arterioscl Thromb 1993; 13: 1449-1455
  • 9 Bochaton-Piallat ML, Gabbiani F, Gabbiani G. Heterogeneity of rat aortic smooth muscle cell replication during development: correlation with replicative activity after experimental endothelial denudation in adults. J Submicroscop Cytol Pathol 1994; 26: 1-8
  • 10 Pauletto P, Chiavegato A, Giuriato L, Scatena M, Faggin E, Grisenti A, Sarzani R, Paci MV, Fulgeri PD, Rappelli A, Pessina AC, Sartore S. Hyperplastic growth of aortic smooth muscle cells in renovascular hypertensive rabbits is characterised by the expansion of an immature cell phenotype. Circ Res 1994; 74: 774-788
  • 11 Lindner V, Giachelli CM, Schwartz SM, Reidy M. A subpopulation of smooth muscle cells in injured rat arteries expresses platelet-derived growth factor-B chain mRNA. Circ Res 1995; 76: 951-957
  • 12 Schwartz SM, de Blois D, O’Brien ERM. The Intima: Soil for Atherosclerosis and Restenosis. Circ Res 1995; 77: 445-465
  • 13 Okamoto E, Imataka K, Fujii J, Kuro-o M, Nakahara K, Nishimura H, Yasaki Y, Nagai R. Heterogeneity in smooth muscle cell population accumulating in the neointimas and the media of poststenotic dilatation of the rabbit carotid artery. Biochem Biophys Res Comm 1992; 185: 459-464
  • 14 Kanthou C, Parry G, Wijelath E, Kakkar VV, Demoliou-Mason C. Thrombin-induced proliferation and expression of platelet-derived growth factor-A chain gene in human vascular smooth muscle cells. FEBS Lett 1992; 314: 143-148
  • 15 Chamley-Campbell J, Campbell GR, Groschel-Stewart U, Bumstock G. FITC-labelled antibody staining of tropomyosin-containing fibrils in smooth, cardiac and skeletal muscle cells, perfusion myoblasts, fibroblasts, endothelial cells and 3T3 cells in culture. Cell and Tissue Research 1977; 183: 153-166
  • 16 Benzakour O, Merzak A, Dooghe Y, Pironin M, Lawrence D, Vigier P. Transforming growth factor beta stimulates mitogenically mouse NIH3T3 fibroblasts and those cells transformed by the EJ-H-ras oncogene. Growth Factors 1992; 6: 265-275
  • 17 Bouck N, Di Mayorca G. Evaluation of chemical carcinogenicity by in vitro neoplastic transformation. In: Cell Culture Jakoby WB, Pastan IH. eds Academic Press Inc; San Diego California: 1979. pp 296-318
  • 18 Leof EB, Proper JA, Goustin AS, Shipley PE, Dicorletto EL, Moses HL. Induction of c-sis mRNA and activity similar to platelet-derived growth factor by transforming growth factor beta. A proposed model for indirect mitogenesis involving autocrine activity. Proc Natl Acad Sci USA 1986; 83: 2453-2457
  • 19 Battegay EJ, Raines EW, Seifert RA, Bowen-Pope DF, Ross R. TGF-beta induces bimodal proliferation of connective tissue cells via complex control of an autocrine PDGF-loop. Cell 1990; 63: 515-524
  • 20 Grainger DJ, Kemp PR, Liu AC, Lawn RM, Metcalf JC. Activation of transforming growth factor-β is inhibited in transgenic apolipoprotein(a) mice. Nature 1994; 370: 460-462
  • 21 MacLeod DC, Strauss BH, de Jong M, Escaned J, Umans VA, van Suylen R-J, Verkerk A, de Feyter PS, Serruys PW. Proliferation and extracellular matrix synthesis of smooth muscle cells cultured from human coronary atherosclerotic and restenotic lesions. J Am Coll Cardiol 1994; 23: 59-65
  • 22 Kanse SM, Wijelath E, Kanthou C, Newman P, Kakkar VV. The proliferative responsiveness of human vascular smooth muscle cells to endothelin correlates with endothelin receptor density. Lab Invest 1995; 72: 376-382
  • 23 San-Antonio JD, Kamovsky MJ, Ottlinger ME, Schilling R, Pukac LA. Isolation of heparin-insensitive aortic smooth muscle cells: Growth and differentiation. Arterioscl Thromb 1993; 13: 748-757