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Scribble regulates an EMT polarity pathway through modulation of MAPK-ERK signaling to mediate junction formation

机译:随意涂抹通过调节MAPK-ERK信号来调节EMT极性途径以介导结形成

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The crucial role the Crumbs and Par polarity complexes play in tight junction integrity has long been established, however very few studies have investigated the role of the Scribble polarity module. Here, we use MCF10A cells, which fail to form tight junctions and express very little endogenous Crumbs3, to show that inducing expression of the polarity protein Scribble is sufficient to promote tight junction formation. We show this occurs through an epithelial-to-mesenchymal (EMT) pathway that involves Scribble suppressing ERK phosphorylation, leading to downregulation of the EMT inducer ZEB. Inhibition of ZEB relieves the repression on Crumbs3, resulting in increased expression of this crucial tight junction regulator. The combined effect of this Scribble-mediated pathway is the upregulation of a number of junctional proteins and the formation of functional tight junctions. These data suggests a novel role for Scribble in positively regulating tight junction assembly through transcriptional regulation of an EMT signaling program.
机译:面包屑和Par极性复合物在紧密连接完整性中起着至关重要的作用,但是很少有研究研究杂乱极性模块的作用。在这里,我们使用MCF10A细胞,它们不能形成紧密的连接并且仅表达很少的内源性Crumbs3,以表明诱导表达极性蛋白Scribble足以促进紧密连接的形成。我们显示这是通过涉及涂鸦抑制ERK磷酸化,导致EMT诱导物ZEB的下调的上皮间质(EMT)途径发生的。 ZEB的抑制可减轻对Crumbs3的抑制,从而导致该关键紧密连接调节因子的表达增加。该自由曲线介导的途径的综合作用是上调许多连接蛋白并形成功能性紧密连接。这些数据表明Scribble在通过EMT信号传导程序的转录调控积极调控紧密连接装配中的新作用。

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