首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Involvement of 14-3-3 Proteins in the Second Epidermal Growth Factor-induced Wave of Rac1 Activation in the Process of Cell Migration
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Involvement of 14-3-3 Proteins in the Second Epidermal Growth Factor-induced Wave of Rac1 Activation in the Process of Cell Migration

机译:14-3-3蛋白参与细胞迁移过程中的第二个表皮生长因子诱导的Rac1激活波。

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摘要

Immense previous efforts have elucidated the core machinery in cell migration, actin remodeling regulated by Rho family small GTPases including RhoA, Cdc42, and Rac1; however, the spatiotemporal regulation of these molecules remains largely unknown. Here, we report that EGF induces biphasic Rac1 activation in the process of cell migration, and UTKO1, a cell migration inhibitor, inhibits the second EGF-induced wave of Rac1 activation but not the first wave. To address the regulation mechanism and role of the second wave of Rac1 activation, we identified 14-3-3ζ as a target protein of UTKO1 and also showed that UTKO1 abrogated the binding of 14-3-3ζ to Tiam1 that was responsible for the second wave of Rac1 activation, suggesting that the interaction of 14-3-3ζ with Tiam1 is involved in this event. To our knowledge, this is the first report to use a chemical genetic approach to demonstrate the mechanism of temporal activation of Rac1.
机译:先前的巨大努力阐明了细胞迁移的核心机制,即由Rho家族小型GTP酶(包括RhoA,Cdc42和Rac1)调控的肌动蛋白重塑。然而,这些分子的时空调控仍然是未知的。在这里,我们报道EGF在细胞迁移过程中诱导双相Rac1激活,而UTKO1,一种细胞迁移抑制剂,抑制第二个EGF诱导的Rac1激活波,但不抑制第一波。为了解决第二次Rac1激活的调控机制和作用,我们确定14-3-3ζ为UTKO1的目标蛋白,并且还表明UTKO1消除了14-3-3ζ与Tiam1的结合,后者是第二次激活的原因。 Rac1激活的高潮,表明14-3-3ζ与Tiam1的相互作用参与了此事件。据我们所知,这是第一个使用化学遗传方法证明Rac1暂时激活机制的报告。

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