Nalluri Sandeep M, O'Connor Joseph W, Gomez Esther W
Department of Chemical Engineering, The Pennsylvania State University, University Park, Pennsylvania, 16802.
Department of Biomedical Engineering, The Pennsylvania State University, University Park, Pennsylvania, 16802.
Cytoskeleton (Hoboken). 2015 Nov;72(11):557-69. doi: 10.1002/cm.21263. Epub 2015 Dec 9.
Epithelial-mesenchymal transition (EMT) is a physiological process that plays an important role in embryonic development and wound healing and is appropriated during pathological conditions including fibrosis and cancer metastasis. EMT can be initiated by a variety of factors, including transforming growth factor (TGF)-β, and is characterized by loss of epithelial features including cell-cell contacts and apicobasal polarity and acquisition of a motile, mesenchymal phenotype. A key feature of EMT is reorganization of the cytoskeleton and recent studies have elucidated regulation mechanisms governing this process. This review describes changes in gene expression patterns of cytoskeletal associated proteins during TGFβ-induced EMT. It further reports TGFβ-induced intracellular signaling cascades that regulate cytoskeletal reorganization during EMT. Finally, it highlights how changes in cytoskeletal architecture during EMT can regulate gene expression, thus further promoting EMT progression.
上皮-间质转化(EMT)是一个生理过程,在胚胎发育和伤口愈合中发挥重要作用,并且在包括纤维化和癌症转移在内的病理状况下会被激活。EMT可由多种因素引发,包括转化生长因子(TGF)-β,其特征是上皮特征丧失,包括细胞间接触和顶-基极性丧失,并获得迁移性的间质表型。EMT的一个关键特征是细胞骨架的重组,最近的研究已经阐明了控制这一过程的调控机制。本综述描述了TGFβ诱导的EMT过程中细胞骨架相关蛋白基因表达模式的变化。它还报道了TGFβ诱导的细胞内信号级联反应,这些反应在EMT过程中调节细胞骨架重组。最后,它强调了EMT过程中细胞骨架结构的变化如何调节基因表达,从而进一步促进EMT进程。