TGF-β Signaling from Receptors to Smads

  1. Ye-Guang Chen2
  1. 1Cardiovascular Research Institute, University of California, San Francisco, San Francisco, California 94143
  2. 2The State Key Laboratory of Membrane Biology, Tsinghua-Peking Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China
  1. Correspondence: akiko.hata{at}ucsf.edu; ygchen{at}tsinghua.edu.cn

Abstract

Transforming growth factor β (TGF-β) and related growth factors are secreted pleiotropic factors that play critical roles in embryogenesis and adult tissue homeostasis by regulating cell proliferation, differentiation, death, and migration. The TGF-β family members signal via heteromeric complexes of type I and type II receptors, which activate members of the Smad family of signal transducers. The main attribute of the TGF-β signaling pathway is context-dependence. Depending on the concentration and type of ligand, target tissue, and developmental stage, TGF-β family members transmit distinct signals. Deregulation of TGF-β signaling contributes to developmental defects and human diseases. More than a decade of studies have revealed the framework by which TGF-βs encode a context-dependent signal, which includes various positive and negative modifiers of the principal elements of the signaling pathway, the receptors, and the Smad proteins. In this review, we first introduce some basic components of the TGF-β signaling pathways and their actions, and then discuss posttranslational modifications and modulatory partners that modify the outcome of the signaling and contribute to its context-dependence, including small noncoding RNAs.



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      1. Cold Spring Harb. Perspect. Biol. 8: a022061 Copyright © 2016 Cold Spring Harbor Laboratory Press; all rights reserved

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