Heterogeneity of smooth muscle cell populations cultured from pig coronary artery

被引:114
作者
Hao, H
Ropraz, P
Verin, V
Camenzind, E
Geinoz, A
Pepper, MS
Gabbiani, G
Bochaton-Piallat, ML
机构
[1] Univ Geneva, Dept Pathol, CMU, CH-1211 Geneva 4, Switzerland
[2] Univ Geneva, Dept Morphol, CMU, CH-1211 Geneva, Switzerland
[3] Univ Hosp Geneva, Div Cardiol, Geneva, Switzerland
关键词
intimal thickening; restenosis; endothelial cells; myosin; smoothelin;
D O I
10.1161/01.ATV.0000022407.91111.E4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-Heterogeneous smooth muscle cell (SMC) populations have been described in the arteries of several species. We have investigated whether SMC heterogeneity is present in the porcine coronary artery, which is widely used as a model of restenosis. Methods and Results-By using 2 isolation methods, distinct medial populations were identified: spindle-shaped SMCs (S-SMCs) after enzymatic digestion, with a "hill-and-valley" growth pattern, and rhomboid SMCs (R-SMCs) after explantation, which grow as a monolayer. Moreover, the intimal thickening that was induced after stent implantation yielded a large proportion of R-SMCs. R-SMCs exhibited high proliferative and migratory activities and high urokinase activity and were poorly differentiated compared with S-SMCs. Heparin and transforming growth factor-beta2 inhibited proliferation and increased differentiation in both populations, whereas fibroblast growth factor-2 and platelet-derived growth factor-BB had the opposite effect. In addition, S-SMCs treated with fibroblast growth factor-2 or platelet-derived growth factor-BB or placed in coculture with coronary artery endothelial cells acquired a rhomboid phenotype. This change was reversible and was also observed with S-SMC clones, suggesting that it depends on phenotypic modulation rather than on selection. Conclusions-Our results show that 2 distinct SMC subpopulations can be recovered from the pig coronary artery media. The study of these subpopulations will be useful for understanding the mechanisms of restenosis.
引用
收藏
页码:1093 / 1099
页数:7
相关论文
共 34 条
[1]  
Angelini G D, 1991, Eur J Vasc Surg, V5, P5, DOI 10.1016/S0950-821X(05)80919-3
[2]  
AU YPT, 1993, HAEMOSTASIS, V23, P177
[3]   SMOOTH-MUSCLE MYOSIN REGULATION BY SERUM AND CELL-DENSITY IN CULTURED RAT LUNG CONNECTIVE-TISSUE CELLS [J].
BABIJ, P ;
ZHAO, J ;
WHITE, S ;
WOODCOCKMITCHELL, J ;
MITCHELL, J ;
ABSHER, M ;
BALDOR, L ;
PERIASAMY, M ;
LOW, RB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (02) :L127-L132
[4]  
Benzakour O, 1996, THROMB HAEMOSTASIS, V75, P854
[5]   CORRELATION BETWEEN THE DISTRIBUTION OF SMOOTH-MUSCLE OR NON MUSCLE MYOSINS AND ALPHA-SMOOTH MUSCLE ACTIN IN NORMAL AND PATHOLOGICAL SOFT-TISSUES [J].
BENZONANA, G ;
SKALLI, O ;
GABBIANI, G .
CELL MOTILITY AND THE CYTOSKELETON, 1988, 11 (04) :260-274
[6]   Plasminogen activator expression in rat arterial smooth muscle cells depends on their phenotype and is modulated by cytokines [J].
Bochaton-Piallat, ML ;
Gabbiani, G ;
Pepper, MS .
CIRCULATION RESEARCH, 1998, 82 (10) :1086-1093
[7]   Phenotypic heterogeneity of rat arterial smooth muscle cell clones - Implications for the development of experimental intimal thickening [J].
BochatonPiallat, ML ;
Ropraz, P ;
Gabbiani, F ;
Gabbiani, G .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1996, 16 (06) :815-820
[8]   THE PHENOTYPES OF SMOOTH-MUSCLE EXPRESSED IN HUMAN ATHEROMA [J].
CAMPBELL, GR ;
CAMPBELL, JH .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1990, 598 :143-158
[9]  
Carmeliet P, 1997, CIRC RES, V81, P829
[10]   Mechanisms of neointima formation and remodeling in the porcine coronary artery [J].
Christen, T ;
Verin, V ;
Bochaton-Piallat, ML ;
Popowski, Y ;
Ramaekers, F ;
Debruyne, P ;
Camenzind, E ;
van Eys, G ;
Gabbiani, G .
CIRCULATION, 2001, 103 (06) :882-888