Osteopontin expression in platelet-derived growth factor-stimulated vascular smooth muscle cells and carotid artery after balloon angioplasty

被引:64
作者
Wang, XK [1 ]
Louden, C [1 ]
Ohlstein, EH [1 ]
Stadel, JM [1 ]
Gu, JL [1 ]
Yue, TL [1 ]
机构
[1] SMITHKLINE BEECHAM PHARMACEUT,DEPT EXPT PATHOL,KING OF PRUSSIA,PA 19406
关键词
osteopontin; platelet-derived growth factor; smooth muscle cell; balloon angioplasty;
D O I
10.1161/01.ATV.16.11.1365
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Osteopontin (OPN), an arginine-glycine-aspartate (RGD)-containing adhesive glycoprotein, is constitutively expressed in rat aorta and carotid arteries and is markedly elevated in response to vascular injury. OPN is chemotactic for vascular smooth muscle cells (SMCs), suggesting a role in vascular remodeling. However, the mechanism for the regulation of OPN expression is poorly understood. In the present study, the effect of platelet-derived growth factor (PDGF) on OPN mRNA expression was investigated in cultured rat aortic SMCs (RASMCs). When RASMCs were stimulated with 1 nmol/L PDGF, a 2.4-fold increase in OPN mRNA expression was observed at 3 hours (P<.05) that peaked at 14 hours with a 6.7-fold increase (P<.001). This induction was blocked by a monoclonal anti-PDGF antibody. Further studies revealed that OPN mRNA expression was induced by PDGF-AB or PDGF-BB but not by PDGF-AA, indicating that only the beta-type PDGF receptor mediates this response. Compared with basic fibroblast growth factor, epidermal growth factor, transforming growth factor-beta, and interleukin-1 beta, PDGF was the most potent factor studied to induce OPN mRNA expression in RASMCs. Immunohistochemical studies demonstrated the elevation of OPN protein in PDGF-stimulated RASMCs. The temporal expression of OPN mRNA after rat carotid artery balloon angioplasty as assessed by both reverse transcription-polymerase chain reaction and Northern blot analysis revealed a 1.5-fold increase at 6 hours (P<.01) that peaked at 1 and 3 days with a 3.1-fold increase (P<.001). Immunohistochemical studies of carotid artery after angioplasty localized OPN expression in the medial SMCs at 1 day, ie, at a rime of significant platelet adherence to the injured vessel, and thereafter to the intimal lesion during neointimal formation. These data suggest that OPN expression in vascular SMCs is regulated by PDGF through the beta-type PDGF receptor in vitro, and possibly in vivo, in situations that involve PDGF released from platelets or other cellular sources, such as blood vessels after angioplasty injury.
引用
收藏
页码:1365 / 1372
页数:8
相关论文
共 26 条
[21]   DEMONSTRATION OF INCREASED ENDOTHELIAL-LEUKOCYTE ADHESION MOLECULE-1 MESSENGER-RNA EXPRESSION IN RAT ISCHEMIC CORTEX [J].
WANG, XK ;
YUE, TL ;
BARONE, FC ;
FEUERSTEIN, GZ .
STROKE, 1995, 26 (09) :1665-1668
[22]   ENHANCED LEUKOCYTE ADHESION TO INTERLEUKIN-1-BETA STIMULATED VASCULAR SMOOTH-MUSCLE CELLS IS MAINLY THROUGH INTERCELLULAR-ADHESION MOLECULE-1 [J].
WANG, XK ;
FEUERSTEIN, GZ ;
CLARK, RK ;
YUE, TL .
CARDIOVASCULAR RESEARCH, 1994, 28 (12) :1808-1814
[23]   Expression of endothelin-1, endothelin-3, endothelin-converting enzyme-1, and endothelin-A and endothelin-B receptor mRNA after angioplasty-induced neointimal formation in the rat [J].
Wang, XK ;
Douglas, SA ;
Louden, C ;
VickeryClark, LM ;
Feuerstein, GZ ;
Ohlstein, EH .
CIRCULATION RESEARCH, 1996, 78 (02) :322-328
[24]  
WANG XK, 1992, J BIOL CHEM, V267, P9176
[25]   OSTEOPONTIN-STIMULATED VASCULAR SMOOTH-MUSCLE CELL-MIGRATION IS MEDIATED BY BETA(3) INTEGRIN [J].
YUE, TL ;
MCKENNA, PJ ;
OHLSTEIN, EH ;
FARACHCARSON, MC ;
BUTLER, WT ;
JOHANSON, K ;
MCDEVITT, P ;
FEUERSTEIN, GZ ;
STADEL, JM .
EXPERIMENTAL CELL RESEARCH, 1994, 214 (02) :459-464
[26]   TISSUE ENDOTHELIN-1 IMMUNOREACTIVITY IN THE ACTIVE CORONARY ATHEROSCLEROTIC PLAQUE - A CLUE TO THE MECHANISM OF INCREASED VASOREACTIVITY OF THE CULPRIT LESION IN UNSTABLE ANGINA [J].
ZEIHER, AM ;
GOEBEL, H ;
SCHACHINGER, V ;
IHLING, C .
CIRCULATION, 1995, 91 (04) :941-947