FLUID SHEAR-STRESS STIMULATES PLATELET-DERIVED GROWTH-FACTOR EXPRESSION IN ENDOTHELIAL-CELLS

被引:109
作者
MITSUMATA, M
FISHEL, RS
NEREM, RM
ALEXANDER, RW
BERK, BC
机构
[1] EMORY UNIV, DEPT MED, DIV CARDIOL, PO DRAWER LL, ATLANTA, GA 30322 USA
[2] GEORGIA INST TECHNOL, SCH MECH ENGN, ATLANTA, GA 30332 USA
[3] GEORGIA INST TECHNOL, HAUT LAB, ATLANTA, GA 30332 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1993年 / 265卷 / 01期
关键词
FLOW; PLATELET-DERIVED GROWTH FACTOR; PROTEIN KINASE-C;
D O I
10.1152/ajpheart.1993.265.1.H3
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Fluid flow and the associated shear stress play a critical role in vascular growth and remodeling. Recent data suggest that increased endothelial cell expression of platelet-derived growth factor (PDGF) A- and B-chain by flow may participate in these events. In the present study, we examined the mechanism for flow-induced PDGF expression, focusing on protein kinase C (PKC). Bovine aortic endothelial cells were exposed to flow (shear stress = 30 dyn/cm2) in a parallel-plate flow chamber. Increases in PDGF B-chain, but not PDGF A-chain, were observed within 3 h, maximal within 6 h (13-fold increase), and sustained for 24 h. PKC appeared to be involved because phorbol 12-myristate 13-acetate induced PDGF B-chain mRNA. Activation of PKC alone, however, was insufficient to induce PDGF mRNA because the selective PKC activator, 1-oleoyl-2-acetyl-sn-glycerol, did not induce PDGF expression. A PKC-independent pathway was suggested by the fact that inhibition of PKC (downregulation with phorbol 12,13-dibutyrate or exposure to staurosporine) failed to block PMA or flow-induced PDGF B-chain expression. These results demonstrate flow-induced PDGF B-chain expression in endothelial cells that appears to be mediated, in part, by a PKC-independent pathway.
引用
收藏
页码:H3 / H8
页数:6
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