The role of endothelin-1 signaling in the fibrosis observed in systemic sclerosis

被引:29
|
作者
Leask, Andrew [1 ]
机构
[1] Univ Western Ontario, Dept Dent, London, ON N6A 5C1, Canada
关键词
Endothelin; Scleroderma; PULMONARY ARTERIAL-HYPERTENSION; CONTROLLED-TRIAL; SKIN FIBROSIS; BOSENTAN; SCLERODERMA; FIBROBLASTS; SILDENAFIL; ET-1; BETA;
D O I
10.1016/j.phrs.2011.01.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Scleroderma (systemic sclerosis, SSc) is an autoimmune disease of unknown etiology characterized by organ fibrosis. There is no therapy for SSc. However, a recent body of evidence strongly implicates endothelin-1 (ET-1) in the pathogenesis of SSc. ET-1 is found in abundance in SSc patients. ET-1 directly induces fibrogenic effects in vitro, and is required for the ability of TGF beta to induce fibrogenic effects both in vitro and in vivo. Moreover, endothelin receptor antagonism reverses key features of the persistent fibrotic phenotype of fibroblasts isolated from lesions of SSc patients. However, clinically, endothelin receptor antagonism alone has had mixed results. This minireview summarizes these observations. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:502 / 503
页数:2
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