Abstract
From observations on 454 coronary arteries from subjects ranging in age from prematurely newborn to 90 years, six structural patterns of medial smooth muscle are interpreted as representing, or related to, the proliferation and/or migration of medial smooth muscle into intima. By measuring the extent of inner medial circumference occupied by four of the six patterns, it was possible to calculate a numerical value designated the medial proliferatice and / or migratory activity (MP-MA) of each artery. During the first three decades, nonatherosclerotic diffuse intimal thickening was the characteristic intimal process, and during this phase of the arterial maturation span, the MP-MA of the arteries was significantly related to the degree of intimal thickening. Following a peak MP-MA level by the end of the third decade, there was a progressive decrease in the MP-MA level as the incidence and severity of atherosclerotic intimal thickening increased. At advanced stages of atherosclerotic intimal thickening, which were associated with thinning of adjacent media, intimal-medial structural patterns indicating a relationship between medial smooth muscle proliferative activity and the expanding atherosclerotic plaque were also apparent. The observations support the concept that the movement of medial smooth muscle into intima is a critical step preceding and during the evolution of the atherosclerotic plaque.
Full text
PDF





















Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Benditt E. P., Benditt J. M. Evidence for a monoclonal origin of human atherosclerotic plaques. Proc Natl Acad Sci U S A. 1973 Jun;70(6):1753–1756. doi: 10.1073/pnas.70.6.1753. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fisher-Dzoga K., Jones R. M., Vesselinovitch D., Wissler R. W. Ultrastructural and immunohistochemical studies of primary cultures of aortic medial cells. Exp Mol Pathol. 1973 Apr;18(2):162–176. doi: 10.1016/0014-4800(73)90014-2. [DOI] [PubMed] [Google Scholar]
- Florentin R. A., Nam S. C., Daoud A. S., Jones R., Scott R. F., Morrison E. S., Kim D. N., Lee K. T., Thomas W. A., Dodds W. J. Dietary-induced atherosclerosis in miniature swine. Exp Mol Pathol. 1968 Jun;8(3):263–301. doi: 10.1016/s0014-4800(68)80001-2. [DOI] [PubMed] [Google Scholar]
- HAUST M. D., MORE R. H., MOVAT H. Z. The role of smooth muscle cells in the fibrogenesis of arteriosclerosis. Am J Pathol. 1960 Oct;37:377–389. [PMC free article] [PubMed] [Google Scholar]
- MOON H. D. Coronary arteries in fetuses, infants, and juveniles. Circulation. 1957 Aug;16(2):263–267. doi: 10.1161/01.cir.16.2.263. [DOI] [PubMed] [Google Scholar]
- Martin G. M., Sprague C. A. Symposium on in vitro studies related to atherogenesis. Life histories of hyperplastoid cell lines from aorta and skin. Exp Mol Pathol. 1973 Apr;18(2):125–141. doi: 10.1016/0014-4800(73)90012-9. [DOI] [PubMed] [Google Scholar]
- Massmann J., Oestreich S. Comparative histological and morphometrical studies into the relevance of intimal thickening to coronary sclerosis. Atherosclerosis. 1976 Sep;24(3):451–456. doi: 10.1016/0021-9150(76)90137-4. [DOI] [PubMed] [Google Scholar]
- PARKER F. An electron microscope study of coronary arteries. Am J Anat. 1958 Sep;103(2):247–273. doi: 10.1002/aja.1001030206. [DOI] [PubMed] [Google Scholar]
- Ross R., Glomset J. A. The pathogenesis of atherosclerosis (second of two parts). N Engl J Med. 1976 Aug 19;295(8):420–425. doi: 10.1056/NEJM197608192950805. [DOI] [PubMed] [Google Scholar]
- Scott R. F., Florentin R. A., Daoud A. S., Morrison E. S., Jones R. M., Hutt M. S. Coronary arteries of children and young adults. A comparison of lipids and anatomic features in New Yorkers and East Africans. Exp Mol Pathol. 1966 Feb;5(1):12–42. doi: 10.1016/0014-4800(66)90003-7. [DOI] [PubMed] [Google Scholar]














