Skip to main content
Log in

Human smooth muscle cells cultured from atherosclerotic plaques and uninvolved vessel wall

  • Published:
In Vitro Aims and scope Submit manuscript

Summary

Smooth muscle cells (SMC) were cultured from atherosclerotic plaques and uninvolved arteries to determine if differences exist between growth characteristics or ultrastructure of the cultured cells. Eighteen aortic punch biopsies provided the uninvolved tissue, and 58 carotid plaques provided the atherosclerotic tissue. Eighty percent of the sample yielded viable cultured cells, which reached a maximum population doubling time during log phase growth of 72 h (seeding density=1.0×104 cells/cm2, 2nd passage). Growth characteristics of both normal and plaque-derived cells were the same in vitro. Growth rate declined with time in culture, and cell division ceased by the 5th or 6th passage. In culture, spindle shaped cells formed the “hill and valley” configuration typical of SMC. Plaquederived SMC were ultrastructurally similar to SMC from uninvolved vessel wall. Proliferative potential did not vary with age of sex, with method of culture, or with whether the cells were plaque derived or not.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Ross, R.; Glomset, J. A. The pathogenesis of atherosclerosis, parts 1 and 2. New Engl. J. Med. 295: 369–380, 420–425; 1976.

    Article  PubMed  CAS  Google Scholar 

  2. Benditt, E. P.; Benditt, J. M.: Evidence for a monoclonal origin of human atherosclerotic plaques. Proc. Natl. Acad. Sci. USA 70: 1753–1756; 1973.

    Article  PubMed  CAS  Google Scholar 

  3. Chamley, J. H.; Campbell, G. R.; McConnell, J. D. Comparison of vascular smooth muscle cells from adult human, monkey and rabbit in primary culture and in subculture. Cell Tissue Res. 177: 503–522; 1977.

    PubMed  CAS  Google Scholar 

  4. Ralston, A.; Wilff, H. S. Mathematical methods for digital computers. New York: Wiley & Sons; 1960: Chapt. 17.

    Google Scholar 

  5. Roscoe, J. T. Fundamental research statistics for the behavioral sciences. 2nd ed. New York: Holt, Rinehart, and Winston, Inc.; 1975: 438.

    Google Scholar 

  6. Barrett, L. A.; Mergner, W. J.; Trump, B. G. Long-term culture of human aortas: development of atherosclerotic-like plaques in serum-supplemented medium. In Vitro 15: 957–966; 1979.

    Article  PubMed  CAS  Google Scholar 

  7. Fowler, S.; Shio, H.; Wolinsky, H. Subcellular fractionation and morphology of calf aortic smooth muscle cells. J. Cell Biol. 75: 166–184; 1977.

    Article  PubMed  CAS  Google Scholar 

  8. Bierman, E. L. The effect of donor age on the in vitro life span of cultured human arterial smooth muscle cells. In Vitro 14: 951–955; 1978.

    Article  PubMed  CAS  Google Scholar 

  9. Moss, N. S., Benditt, E. P. Human atherosclerotic plaque cells and leiomyoma cells. Comparison ofin vitro growth characteristics. Am. J. Pathol. 78: 175–185; 1975.

    PubMed  CAS  Google Scholar 

  10. Schneider, E. L.; Mitusui, Y. The relationship betweenin vitro cellular aging andin vivo human age. Proc. Natl. Acad. Sci. USA. 73: 3584–3588; 1976.

    Article  PubMed  CAS  Google Scholar 

  11. Martin, G. M.; Sprague, C. A. Symposium onin vitro studies related to atherogenesis, life histories of hyperplastoid cell lines from aorta and skin. Exp. Mol. Pathol. 18: 125–141; 1973.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This study was supported in part by National Institutes of Health Grant HL-17269

Rights and permissions

Reprints and permissions

About this article

Cite this article

Eskin, S.G., Sybers, H.D., Lester, J.W. et al. Human smooth muscle cells cultured from atherosclerotic plaques and uninvolved vessel wall. In Vitro 17, 713–718 (1981). https://doi.org/10.1007/BF02628408

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02628408

Key words

Navigation