Peculiarities of cell composition and cell proliferation in different type atherosclerotic lesions in carotid and coronary arteries

Atherosclerosis

Volumn 212, Issue 2, 2010, Pages 436-443

  Orekhov, A N ^a,b,c   Andreeva, E R ^c   Andrianova, I V ^c   Bobryshev, Y V ^d  

^a Institute of Chemical Problems of Ecology   (Russian Federation)

^b INSTITUTE OF GENERAL PATHOLOGY AND PATHOPHYSIOLOGY   (Russian Federation)

^c INSTITUTE OF EXPERIMENTAL CARDIOLOGY   (Russian Federation)

^d UNIVERSITY OF NEW SOUTH WALES   (Australia)

Author keywords

Aorta; Carotid artery; Coronary artery; Hematogenous cells; Inflammation; Proliferation

Indexed keywords

ADULT; AGED; AORTA; ARTERIAL WALL THICKNESS; ARTICLE; ATHEROGENESIS; ATHEROSCLEROTIC PLAQUE; CAROTID ARTERY; CELL ACTIVITY; CELL COMPOSITION; CELL COUNT; CELL PROLIFERATION; CELLULAR DISTRIBUTION; CONTROLLED STUDY; CORONARY ARTERY; FEMALE; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; INFLAMMATORY CELL; MALE; OUTCOME ASSESSMENT; PRIORITY JOURNAL;

ADULT; AGED; AORTA; ARTERIES; ATHEROSCLEROSIS; CAROTID ARTERIES; CELL PROLIFERATION; CORONARY VESSELS; DISEASE PROGRESSION; FEMALE; HUMANS; INFLAMMATION; MALE; MIDDLE AGED; TUNICA INTIMA;

EID: 77957691565     PISSN: 00219150     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.atherosclerosis.2010.07.009     Document Type: Article

References (38)

1. Ross R. Atherosclerosis-an inflammatory disease. N Engl J Med 1999, 340:115-126.
2. Hansson G.K. Atherosclerosis-an immune disease: the Anitschkov lecture 2007. Atherosclerosis 2009, 202:2-10.
3. Orekhov A.N., Andreeva E.R., Krushinsky A.V., et al. Intimal cells and atherosclerosis. Relationship between the number of intimal cells and major manifestations of atherosclerosis in the human aorta. Am J Pathol 1986, 125:402-415.
4. Gordon D., Schwartz S.M., Benditt E.P., Wilcox J.N. Growth factors and cell proliferation in human atherosclerosis. Transplant Proc 1989, 21:3692-3694.
5. Gordon D., Reidy M.A., Benditt E.P., Schwartz S.M. Cell proliferation in human coronary arteries. Proc Natl Acad Sci USA 1990, 87:4600-4604.
6. Rekhter M.D., Gordon D. Cell proliferation and collagen synthesis are two independent events in human atherosclerotic plaques. J Vasc Res 1994, 31:280-286.
7. Rekhter M.D., Gordon D. Active proliferation of different cell types, including lymphocytes, in human atherosclerotic plaques. Am J Pathol 1995, 147:668-677.
8. Orekhov A.N., Andreeva E.R., Mikhailova I.A., Gordon D. Cell proliferation in normal and atherosclerotic human aorta: proliferative splash in lipid-rich lesions. Atherosclerosis 1998, 139:41-48.
9. Góis J., Higuchi M., Reis M., et al. Infectious agents, inflammation, and growth factors: how do they interact in the progression or stabilization of mild human atherosclerotic lesions?. Ann Vasc Surg 2006, 20:638-645.
10. Hanke H., Lenz C., Finking G. The discovery of the pathophysiological aspects of atherosclerosis-a review. Acta Chir Belg 2001, 101:162-169.
11. Andreeva E.R., Pugach I.M., Orekhov A.N. Collagen-synthesizing cells in initial and advanced atherosclerotic lesions of human aorta. Atherosclerosis 1997, 130:133-142.
12. Manolakou P., Angelopoulou R., Bakoyiannis C., et al. Cellular proliferation in complicated versus uncomplicated atherosclerotic lesions: total cell population, foam cells and newly formed microvessels. Tissue Cell 2009, 41:408-413.
13. Fuster J.J., Fernández P., González-Navarro H., Silvestre C., Nabah Y.N., Andrés V. Control of cell proliferation in atherosclerosis: insights from animal models and human studies. Cardiovasc Res 2010, 86:254-264.
14. Stary H.C., Chandler A.B., Glagov S., et al. A definition of initial, fatty streak, and intermediate lesions of atherosclerosis. A report from the Committee on Vascular Lesions of the Council on Arteriosclerosis, American Heart Association. Circulation 1994, 89:2462-2478.
15. Stary H.C., Chandler A.B., Dinsmore R.E., et al. A definition of advanced types of atherosclerotic lesions and a histological classification of atherosclerosis. A report from the Committee on Vascular Lesions of the Council on Arteriosclerosis, American Heart Association. Circulation 1995, 92:1355-1374.
16. Babaev V.R., Bobryshev Y.V., Stenina O.V., Tararak E.M., Gabbiani G. Heterogeneity of smooth muscle cells in atheromatous plaque of human aorta. Am J Pathol 1990, 136:1031-1042.
17. Babaev V.R., Bobryshev Y.V., Sukhova G.K., Kasantseva I.A. Monocyte/macrophage accumulation and smooth muscle cell phenotypes in early atherosclerotic lesions of human aorta. Atherosclerosis 1993, 100:237-248.
18. Bobryshev Y.V., Lord R.S. Langhans cells of human arterial intima: uniform by stellate appearance but different by nature. Tissue Cell 1996, 28:177-194.
19. Poston R.N., Hussain I.F. The immunohistochemical heterogeneity of atheroma macrophages: comparison with lymphoid tissues suggests that recently blood-derived macrophages can be distinguished from longer-resident cells. J Histochem Cytochem 1993, 41:1503-1512.
20. Vanderlaan P.A., Reardon C.A. The unusual suspects: an overview of the minor leukocyte populations in atherosclerosis. J Lipid Res 2005, 46:829-838.
21. Galkina E., Ley K. Leukocyte influx in atherosclerosis. Curr Drug Targets 2007, 8:1239-1248.
22. Weber C., Zernecke A., Libby P. The multifaceted contributions of leukocyte subsets to atherosclerosis: lessons from mouse models. Nat Rev Immunol 2008, 8:802-815.
23. Pepine C.J., Nichols W.W. Estrogen and different aspects of vascular disease in women and men. Circ Res 2006, 99:459-461.
24. Hansson G.K. Inflammation, atherosclerosis, and coronary artery disease. N Engl J Med 2005, 352:1685-1695.
25. Bobryshev Y.V. Monocyte recruitment and foam cell formation in atherosclerosis. Micron 2006, 37:208-222.
26. Galkina E., Ley K. Immune and inflammatory mechanisms of atherosclerosis. Annu Rev Immunol 2009, 27:165-197.
27. Shimada K. Immune system and atherosclerotic disease. Heterogeneity of leukocyte subsets participating in the pathogenesis of atherosclerosis. Circ J 2009, 73:994-1001.
28. Tertov V.V., Orekhov A.N., Hwa Ryong L., Smirnov V.N. Intracellular cholesterol accumulation is accompanied by enhanced proliferative activity of human aortic intimal cells. Tissue Cell 1988, 20:849-854.
29. Orekhov A.N., Tertov V.V., Kudryashov S.A., Smirnov V.N. Triggerlike stimulation of cholesterol accumulation and DNA and extracellular matrix synthesis induced by atherogenic serum or low density lipoprotein in cultured cells. Circ Res 1990, 66:311-320.
30. Hartvigsen K., Chou M.Y., Hansen L.F., Shaw P.X., Tsimikas S., Binder C.J., et al. The role of innate immunity in atherogenesis. J Lipid Res 2009, 50(Suppl.):S388-S393.
31. Orekhov A.N., Tertov V.V., Kabakov A.E., Adamova I.Yu., Pokrovsky S.N., Smirnov V.N. Autoantibodies against modified low density lipoprotein. Nonlipid factor of blood plasma that stimulates foam cell formation. Arterioscler Thromb 1991, 11:316-326.
32. Freigang S., Hörkkö S., Miller E., Witztum J.L., Palinski W. Immunization of LDL receptor-deficient mice with homologous malondialdehyde-modified and native LDL reduces progression of atherosclerosis by mechanisms other than induction of high titers of antibodies to oxidative neoepitopes. Arterioscler Thromb Vasc Biol 1998, 18:1972-1982.
33. Orekhov A.N., Kosykh V.A., Repin V.S., Smirnov V.N. Cell proliferation in normal and atherosclerotic human aorta. II. Autoradiographic observation on deoxyribonucleic acid synthesis in primary cell culture. Lab Invest 1983, 48:749-754.
34. Zhao G.F., Seng J.J., Zhang H., She M.P. Effects of oxidized low density lipoprotein on the growth of human artery smooth muscle cells. Chin Med J (Engl) 2005, 118:1973-1978.
35. Ulrich-Merzenich G., Metzner C., Bhonde R.R., Malsch G., Schiermeyer B., Vetter H. Simultaneous isolation of endothelial and smooth muscle cells from human umbilical artery or vein and their growth response to low-density lipoproteins. In Vitro Cell Dev Biol Anim 2002, 38:265-272.
36. Watanabe T., Pakala R., Katagiri T., Benedict C.R. Mildly oxidized low-density lipoprotein acts synergistically with angiotensin II in inducing vascular smooth muscle cell proliferation. J Hypertens 2001, 19:1065-1073.
37. Bobryshev Y.V., Babaev V.R., Lord R.S., Watanabe T. Cell death in atheromatous plaque of the carotid artery occurs through necrosis rather than apoptosis. In Vivo 1997, 11:441-452.
38. Zhu S.N., Chen M., Jongstra-Bilen J., Cybulsky M.I. GM-CSF regulates intimal cell proliferation in nascent atherosclerotic lesions. J Exp Med 2009, 206:2141-2149.