Heterogeneous smooth muscle cell population derived from small and larger arteries

被引:27
作者
Nakamura, A [1 ]
Isoyama, S
Watanabe, T
Katoh, M
Sawai, T
机构
[1] Tohoku Univ, Sch Med, Dept Internal Med 1, Sendai, Miyagi 98077, Japan
[2] Tohoku Univ, Sch Med, Dept Pathol 1, Sendai, Miyagi 98077, Japan
[3] Tohoku Univ Hosp, Dept Pathol, Sendai, Miyagi 98077, Japan
关键词
heterogeneity; rat; smooth muscle cells; stretch; platelet-derived growth factor;
D O I
10.1006/mvre.1997.2050
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Vascular lesion formations in such disease states as hypertension and atherosclerosis occur in a district-specific manner. Large conduit and small resistance arteries play district-specific roles in the regulation of organ perfusion. Using a culture method, we studied the morphology and growth of smooth muscle cells derived from small arteries (S-SMCs, less than 90 mu m in internal diameter) and from larger arteries (L-SMCs, ranging from 800 to 900 mu m) of the rat mesenteric arterial bed. S-SMCs showed a hill-and-valley pattern, whereas L-SMCs showed sheet or whorl formation. The majority of S-SMCs were smaller, bipolar-shaped; in contrast, the majority of L-SMCs were larger, polygonal-shaped. Actin fibers within S-SMCs were oriented in a bipolar manner from the nuclei, whereas those within L-SMCs had a radial appearance. [H-3]Thymidine incorporation induced by serum, platelet-derived growth factor-AB (PDGF), or mechanical stretch was greater in S- vs L-SMCs. The population doubling time measured after the addition of serum or PDGF was shorter in S- vs L-SMCs. Thus, distinct morphological and growth phenotypes of SMCs exist in small and larger arteries of the same vascular bed. (C) 1998 Academic Press.
引用
收藏
页码:14 / 28
页数:15
相关论文
共 33 条
[1]   NA+-K+-ATPASE IN RAT VASCULAR SMOOTH-MUSCLE CELL GROWN-INVITRO [J].
AVIV, A ;
HIGASHINO, H ;
HENSTEN, D ;
BAUMAN, JW ;
LUBIT, BW ;
SEARLE, BM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1983, 244 (03) :C227-C233
[2]   MIGRATORY ACTIVITY OF HUMAN SMOOTH-MUSCLE CELLS CULTIVATED FROM CORONARY AND PERIPHERAL PRIMARY AND RESTENOTIC LESIONS REMOVED BY PERCUTANEOUS ATHERECTOMY [J].
BAURIEDEL, G ;
WINDSTETTER, U ;
DEMAIO, SJ ;
KANDOLF, R ;
HOFLING, B .
CIRCULATION, 1992, 85 (02) :554-564
[3]   ANGIOTENSIN-II-STIMULATED PROTEIN-SYNTHESIS IN CULTURED VASCULAR SMOOTH-MUSCLE CELLS [J].
BERK, BC ;
VEKSHTEIN, V ;
GORDON, HM ;
TSUDA, T .
HYPERTENSION, 1989, 13 (04) :305-314
[4]  
BLAES N, 1991, IN VITRO CELL DEV B, V27, P725
[5]   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
[6]   INFLUENCE OF HYPERTENSION ON AORTIC ATHEROSCLEROSIS IN THE WATANABE RABBIT [J].
CHOBANIAN, AV ;
LICHTENSTEIN, AH ;
NILAKHE, V ;
HAUDENSCHILD, CC ;
DRAGO, R ;
NICKERSON, C .
HYPERTENSION, 1989, 14 (02) :203-209
[7]   MONOCLONAL-ANTIBODIES TO DESMIN, THE MUSCLE-SPECIFIC INTERMEDIATE FILAMENT PROTEIN [J].
DEBUS, E ;
WEBER, K ;
OSBORN, M .
EMBO JOURNAL, 1983, 2 (12) :2305-2312
[8]  
DREHER KL, 1991, EUR J CELL BIOL, V54, P1
[9]   CULTURE OF RENAL ARTERIOLAR SMOOTH-MUSCLE CELLS - MITOGENIC RESPONSES TO ANGIOTENSIN-II [J].
DUBEY, RK ;
ROY, A ;
OVERBECK, HW .
CIRCULATION RESEARCH, 1992, 71 (05) :1143-1152
[10]   VASCULAR BIOLOGY AND MEDICINE IN THE 1990S-SCOPE, CONCEPTS, POTENTIALS, AND PERSPECTIVES [J].
DZAU, VJ ;
GIBBONS, GH ;
COOKE, JP ;
OMOIGUI, N .
CIRCULATION, 1993, 87 (03) :705-719