Attisano Liliana, Wrana Jeffrey L
Department of Anatomy and Cell Biology, University of Toronto, Toronto M5S 1A8, Canada.
Science. 2002 May 31;296(5573):1646-7. doi: 10.1126/science.1071809.
Transforming growth factor-beta (TGF-beta) superfamily members regulate a plethora of developmental processes, and disruption of their activity has been implicated in a variety of human diseases ranging from cancer to chondrodysplasias and pulmonary hypertension. Intense investigations have revealed that SMAD proteins constitute the basic components of the core intracellular signaling cascade and that SMADs function by carrying signals from the cell surface directly to the nucleus. Recent insights have revealed how SMAD proteins themselves are regulated and how appropriate subcellular localization of SMADs and TGF-beta transmembrane receptors is controlled. Current research efforts investigating the contribution of SMAD-independent pathways promise to reveal advances to enhance our understanding of the signaling cascade.
转化生长因子-β(TGF-β)超家族成员调节众多发育过程,其活性的破坏与从癌症到软骨发育不全和肺动脉高压等多种人类疾病有关。深入研究表明,SMAD蛋白构成核心细胞内信号级联反应的基本成分,且SMAD蛋白通过将信号从细胞表面直接传递到细胞核发挥作用。最近的研究揭示了SMAD蛋白自身是如何被调节的,以及SMAD蛋白和TGF-β跨膜受体的适当亚细胞定位是如何被控制的。目前对不依赖SMAD途径作用的研究工作有望取得进展,以增进我们对信号级联反应的理解。