Dynamics of TGF-β/Smad signaling

被引:160
作者
Zi, Zhike [2 ]
Chapnick, Douglas A. [1 ]
Liu, Xuedong [1 ]
机构
[1] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
[2] Univ Freiburg, BIOSS Ctr Biol Signalling Studies, D-79104 Freiburg, Germany
基金
美国国家卫生研究院;
关键词
TGF-beta; Smad; Mathematical model; Dose-response; Switch-like response; GROWTH-FACTOR-BETA; RECEPTOR INTERNALIZATION; PARAMETER-ESTIMATION; ENDOCYTIC REGULATION; KINETIC-ANALYSIS; FEEDBACK LOOPS; SMAD; SNON; ACTIVATION; TRANSCRIPTION;
D O I
10.1016/j.febslet.2012.03.063
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 physiological responses to TGF-beta stimulation are diverse and vary amongst different cell types and environmental conditions. Even though the principal molecular components of the canonical and the non-canonical TGF-beta signaling pathways have been largely identified, the mechanism that underlies the well-established context dependent physiological responses remains a mystery. Understanding how the components of TGF-beta signaling function as a system and how this system functions in the context of the global cellular regulatory network requires a more quantitative and systematic approach. Here, we review the recent progress in understanding TGF-beta biology using integration of mathematical modeling and quantitative experimental analysis. These studies reveal many interesting dynamics of TGF-beta signaling and how cells quantitatively decode variable doses of TGF-beta stimulation. (C) 2012 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1921 / 1928
页数:8
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