TGFβ, cardiac fibroblasts, and the fibrotic response

被引:224
作者
Leask, Andrew [1 ]
机构
[1] Univ Western Ontario, CIHR Grp Skeletal Dev & Remodeling, Div Oral Biol, London, ON N6A 5C1, Canada
[2] Univ Western Ontario, Dept Physiol & Pharmacol, Schulich Sch Med & Dent, London, ON N6A 5C1, Canada
基金
加拿大健康研究院; 加拿大创新基金会;
关键词
TGFbeta; fibrosis; endothelin; CTGF;
D O I
10.1016/j.cardiores.2006.07.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The cytokine transforming growth factor beta (TGF beta) is a major contributor to fibrogenic responses both in vitro and in vivo. TGF beta possesses many functions; thus, broadly targeting TGF beta signaling as an anti-fibrotic approach is anticipated to be problematic. Recent experiments, however, have begun to elucidate the signaling pathways through which TGF beta activates a fibrotic program. This review critically evaluates the evidence supporting TGF beta as a pro-fibrotic cytokine, with special attention to cardiac fibrosis, and suggests several possible points for selective drug intervention to combat chronic fibrotic disease. (c) 2006 European Society of Cardiology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:207 / 212
页数:6
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