The TGFβ superfamily in stern cell biology and early mammalian embryonic development

被引:72
作者
Beyer, Tobias A. [1 ]
Narimatsu, Masahiro [1 ]
Weiss, Alexander [1 ]
David, Laurent [1 ]
Wrana, Jeffrey L. [1 ,2 ]
机构
[1] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Ctr Syst Biol, Toronto, ON M5G 1X5, Canada
[2] Univ Toronto, Dept Mol Genet, Toronto, ON, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2013年 / 1830卷 / 02期
基金
瑞士国家科学基金会;
关键词
TGFbeta family; SMAD; Cell fate; Pluripotency; Stem cell; PRIMORDIAL GERM-CELLS; SELF-RENEWAL; UBIQUITIN LIGASE; MOUSE EMBRYOS; GROWTH-FACTOR; HUMAN ES; TRANSCRIPTIONAL ACTIVATION; NEURAL DIFFERENTIATION; SIGNAL-TRANSDUCTION; NODAL EXPRESSION;
D O I
10.1016/j.bbagen.2012.08.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Background: Members of the Transforming Growth Factor-beta (TGF beta) superfamily of cytokines are essential for early embryonic development and play crucial roles in pluripotency and differentiation of embryonic stem cells in vitro. Scope of review: In this review, we discuss how TGF beta. family signals are read by cells and how they are modulated by the cellular context Furthermore, we review recent advances in our understanding of TGF beta function in embryonic stem cells and point out hot topics at the intersection of TGF beta signaling and stem cell biology fields. Major conclusion: TGF beta family signals are essential for early mammalian development and the importance of this pathway is reflected in pluripotent stem cells derived from the mammalian embryo. General significance: Understanding signaling pathways underlying pluripotency and cell fate specification holds promises for the advent of personalized regenerative medicine. This article is part of a Special Issue entitled Biochemistry of Stem Cells. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:2268 / 2279
页数:12
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