Regulation of PDGF and its receptors in fibrotic diseases

被引:633
作者
Bonner, JC [1 ]
机构
[1] NIEHS, Res Triangle Pk, NC 27709 USA
关键词
PDGF; fibrosis; lung; liver; kidney;
D O I
10.1016/j.cytogfr.2004.03.006
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
Plate] et-derived growth factor (PDGF) isoforms play a major role in stimulating the replication, survival, and migration of myofibroblasts during the pathogenesis of fibrotic diseases. During fibrogenesis, PDGF is secreted by a variety of cell types as a response to injury, and many pro-inflammatory cytokines mediate their mitogenic effects via the autocrine release of PDGF. PDGF action is determined by the relative expression of PDGF alpha-receptors (PDGFRalpha) and beta-receptors (PDGFRbeta) on the surface of myofibroblasts. These receptors are induced during fibrogenesis, thereby amplifying biological responses to PDGF isoforms. PDGF action is also modulated by extracellular binding proteins and matrix molecules. This review summarizes the literature on the role of PDGF and its receptors in the development of fibrosis in a variety of organ systems, including lung, liver, kidney, and skin. (C) 2004 Published by Elsevier Ltd.
引用
收藏
页码:255 / 273
页数:19
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