Transforming growth factor beta is a modulator of platelet-derived growth factor action in vascular smooth muscle cells: A possible role for catalase activity and glutathione peroxidase activity

被引:19
|
作者
Nishio, E
Watanabe, Y
机构
[1] Department of Pharmacology, National Defense Medical College, Tokorozawa, Saitama, 359, 3-2, Namiki
关键词
D O I
10.1006/bbrc.1997.6213
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transforming growth factor-beta (TGF-beta) has been implicated in mediating the growth of vascular smooth muscle cells (VSMCs) after vascular injury. In this study, we examined the mechanism underlying the growth-modulating effects of TGF-beta in confluent VSMCs. Stimulation of rat VSMC by TGF-beta decreased both their catalase activity and glutathione peroxidase activity in a dose-dependent manner. In mitogenesis assays using the confluent cells, TGF-beta was not a direct mitogen for VSMC, but potentiated the stimulatory effect of platelet-derived growth factor (PDGF)-BB. This enhancement of mitogenesis was blunted by the addition of the scavenging enzyme catalase or the chemical antioxidant N-acetyl-L-cysteine. In summary, TGF-beta enhances the mitogenic effect response of PDGF-BB, largely depending on the dysregulation of catalase activity and glutathione peroxidase activity by TGF-beta. (C) 1997 Academic Press.
引用
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页码:1 / 4
页数:4
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