Mammalian transforming growth factor-βs:: Smad signaling and physio-pathological roles

被引:145
|
作者
Javelaud, D [1 ]
Mauviel, A [1 ]
机构
[1] Univ Paris 07, Hop St Louis, INSERM, U532,Inst Rech Peau, Pavillon Bazin 1,Ave Claude Vellefaux, F-75010 Paris, France
来源
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY | 2004年 / 36卷 / 07期
关键词
transforming growth factor-beta; smad signaling; bone morphogenic proteins;
D O I
10.1016/S1357-2725(03)00255-3
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
Since its discovery in the early 1980s, transforming growth factor-beta (TGF-beta) has emerged as a family of growth factors involved in essential physiological processes, including embryonic development, differentiation, tissue repair and cell growth control. Knockout experiments for the three mammalian isoforms of TGF-betas in mice have demonstrated their importance in regulating inflammation and tissue repair. Also, TGF-beta has been implicated in the pathogenesis of human diseases, including tissue fibrosis and carcinogenesis where, in the latter case, it may exert both tumor suppressor and pro-oncogenic activities depending on the stage of the tumor. Cellular signaling by TGF-beta family members is initiated by the assembly of specific cell surface serine/threonine kinase type receptors that activate transcription factors of the Smad family. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1161 / 1165
页数:5
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