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首页> 外文期刊>The FEBS journal >Cytokine-induced macropinocytosis in macrophages is regulated by 14-3-3 zeta through its interaction with serine-phosphorylated coronin 1
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Cytokine-induced macropinocytosis in macrophages is regulated by 14-3-3 zeta through its interaction with serine-phosphorylated coronin 1

机译:细胞因子诱导的巨噬细胞在巨噬细胞中的作用是通过14-3-3 zeta与丝氨酸磷酸化冠心蛋白1的相互作用来调节的

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The induction of macropinocytosis in macrophages during an inflammatory response is important for clearance of pathogenic microbes as well as the generation of appropriate immune responses. Recent data suggest that cytokine stimulation of macrophages induces macropinocytosis through phosphorylation of the protein coronin 1, thereby redistributing coronin 1 from the cell cortex to the cytoplasm followed by the activation of phosphoinositol-3 (PI-3) kinase. However, how coronin 1 phosphorylation regulates these processes remains unclear. We here define an essential role for 14-3-3 in cytokine-induced and coronin-1-dependent macropinocytosis in macrophages. We found that, upon stimulation, phosphorylated coronin 1 transiently associated with 14-3-3 and receptor of activated C kinase 1 (RACK1). Importantly, downregulation of 14-3-3, but not RACK1, prevented relocation of coronin 1, as well as the induction of PI-3 kinase activity and thereby macropinocytosis upon cytokine stimulation. Together these data define an essential role for 14-3-3 in the regulation of macropinocytosis in macrophages upon cytokine stimulation through modulation of the localization of coronin 1.
机译:在炎症反应过程中巨噬细胞巨噬细胞的诱导对于清除病原微生物以及产生适当的免疫反应非常重要。最近的数据表明巨噬细胞的细胞因子刺激通过冠状蛋白1的磷酸化诱导巨噬细胞增多,从而将冠状蛋白1从细胞皮层重新分配到细胞质,然后激活磷酸肌醇3(PI-3)激酶。然而,冠状蛋白1的磷酸化如何调节这些过程仍不清楚。我们在这里定义14-3-3在巨噬细胞中的细胞因子诱导和冠状蛋白1依赖性巨胞饮作用中的重要作用。我们发现,经刺激后,磷酸化的冠状蛋白1与14-3-3和活化的C激酶1(RACK1)的受体短暂相关。重要的是,下调14-3-3而不是RACK1可以阻止冠状蛋白1的重新定位,并防止PI-3激酶活性的诱导,从而阻止细胞因子刺激后的巨胞饮作用。这些数据共同定义了14-3-3在通过调节冠蛋白1的位置来刺激细胞因子刺激巨噬细胞中巨噬细胞的调控中的重要作用。

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