New regulatory mechanisms of TGF-β receptor function

被引:314
作者
Kang, Jong Seok
Liu, Cheng
Derynck, Rik [1 ]
机构
[1] Univ Calif San Francisco, Dept Cell & Tissue Biol, Cell Biol Program, San Francisco, CA 94143 USA
关键词
GROWTH-FACTOR-BETA; PROTEIN PHOSPHATASE 2A; FYVE DOMAIN PROTEIN; I RECEPTOR; UBIQUITIN LIGASE; SMAD1/5; PHOSPHORYLATION; PML FUNCTION; KINASE; ACTIVATION; INTERNALIZATION;
D O I
10.1016/j.tcb.2009.05.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Transforming growth factor-beta (TGF-beta) regulates cell proliferation, differentiation and apoptosis, and TGF-beta-related proteins have key roles in development, tissue homeostasis and disease. Upon binding to their cell surface receptors, TGF-beta family proteins signal through Smads to induce changes in gene expression. TGF-beta-induced Smad signaling and additional non-Smad pathways have been studied extensively in an effort to understand the complex and versatile responses to TGF-beta family proteins. Recently, it has become increasingly apparent that the signaling responses are also extensively defined by regulatory mechanisms at the level of the receptors themselves. Here, we discuss recent insights into the effects of post-translational modifications, protein associations and mode of internalization on the functions of the TGF-beta receptors and their signaling responses.
引用
收藏
页码:385 / 394
页数:10
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