Orthopedic Hospital Research Center, Department of Orthopedic Surgery, University of California-Los Angeles, Los Angeles, CA 90095, United States.
Cytokine Growth Factor Rev. 2009 Oct-Dec;20(5-6):379-88. doi: 10.1016/j.cytogfr.2009.10.010.
Smad proteins are intracellular molecules that mediate the canonical signaling cascade of TGFbeta superfamily growth factors. The TGFbeta superfamily comprises two groups of growth factors, BMPs and TGFbetas. Both groups can be further divided into several sub-groups based on sequence homologies and functional similarities. Ligands of the TGFbeta superfamily bind to cell surface receptors to activate Smad proteins in the cytoplasm; then the activated Smad proteins translocate into the nucleus to activate or repress specific target gene transcription. Both groups of growth factors play important roles in skeletal development and regeneration. However, whether these effects reflect signaling through canonical Smad pathways, or other non-canonical signaling pathways in vivo remains a mystery. Moreover, the mechanisms utilized by Smad proteins to initiate nuclear events and their interactions with cytoplasmic proteins are still under intensive investigation. This review will discuss the most recent progress understanding Smad signaling in the context of skeletal development and regeneration.
Smad 蛋白是细胞内分子,可介导 TGFβ 超家族生长因子的经典信号级联反应。TGFβ 超家族由两组生长因子组成,即 BMPs 和 TGFβs。这两组生长因子都可以根据序列同源性和功能相似性进一步分为几个亚组。TGFβ 超家族的配体与细胞表面受体结合,在细胞质中激活 Smad 蛋白;然后,激活的 Smad 蛋白易位到细胞核中,激活或抑制特定的靶基因转录。这两组生长因子在骨骼发育和再生中都发挥着重要作用。然而,这些作用是否反映了体内通过经典 Smad 途径的信号传递,还是其他非经典信号途径,目前仍是一个谜。此外,Smad 蛋白用于启动核事件的机制及其与细胞质蛋白的相互作用仍在深入研究中。本文将讨论关于 Smad 信号在骨骼发育和再生方面的最新研究进展。