Curcumin suppresses TGF-β signaling by inhibition of TGIF degradation in scleroderma fibroblasts

被引:39
|
作者
Song, Kemin [1 ]
Peng, Shaowen [1 ]
Sun, Zheng [2 ]
Li, Haitao [1 ]
Yang, Rongya [1 ]
机构
[1] Beijing Mil Command Gen Hosp PLA, Dept Dermatol & Venerol, Beijing 100125, Peoples R China
[2] Capital Med Univ, Luhe Teaching Hosp, Dept Dermatol & Venerol, Beijing 101149, Peoples R China
关键词
Scleroderma fibroblasts; Curcumin; TGF-beta; TGIF; FIBROSIS; EXPRESSION; THERAPY; CHEMOPREVENTION; RECEPTORS; SMAD2; CELLS; RATS;
D O I
10.1016/j.bbrc.2011.07.044
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
The transforming transforming growth factor-beta (TGF-beta) signaling pathway plays a key role in the fibrotic process in systemic scleroderma (SSc). Curcumin, a Turmeric root extract, has been demonstrated to exert antifibrotic activity. In the present study, we carefully investigated the effect of curcumin on TGF-beta signaling and its potential mechanism in SSc fibroblasts. We demonstrated a potent inhibitory effect of curcumin on TGF-beta signaling. Curcumin counteracted TGF-beta-induced phosphorylation of Smad2 but not Smad3. Further study revealed curcumin induced upregulation of TGF-beta-induced factor (TGIF), a negative regulator of TGF-beta signaling. The TGIF silencing results evidenced the essential role of TGIF in curcumin-mediated TGF-beta/Smad2 suppression. Moreover, our data indicated that the upregulation of TGIF by curcumin might result from decreased ubiquitination of TGIF, which blocks its proteasome-mediated degradation. Collectively, our data provide a novel mechanism of curcumin-mediated suppression of fibrotic process in scleroderma. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:821 / 825
页数:5
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