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内体运输和表皮生长因子受体的降解需要磷脂酰肌醇4激酶。

Phosphatidylinositol 4-kinase is required for endosomal trafficking and degradation of the EGF receptor.

作者信息

Minogue Shane, Waugh Mark G, De Matteis Maria Antonietta, Stephens David J, Berditchevski Fedor, Hsuan J Justin

机构信息

Centre for Molecular Cell Biology, Department of Medicine, Royal Free and University College Medical School, University College London, Rowland Hill Street, London, NW3 2PF, UK.

出版信息

J Cell Sci. 2006 Feb 1;119(Pt 3):571-81. doi: 10.1242/jcs.02752.

Abstract

The type II alpha isoform of phosphatidylinositol 4-kinase has recently been shown to function in the recruitment of adaptor protein-1 complexes to the trans-Golgi network. Here we show that phosphatidylinositol 4-kinase IIalpha is also a component of highly dynamic membranes of the endosomal system where it colocalises with protein markers of the late endosome and with endocytosed epidermal growth factor. When phosphatidylinositol 4-kinase IIalpha activity was inhibited in vivo using the monoclonal antibody 4C5G or by depression of endogenous phosphatidylinositol 4-kinase IIalpha protein levels using RNA interference, ligand-bound epidermal growth factor receptor failed to traffic to late endosomes and instead accumulated in vesicles in a sub-plasma membrane compartment. Furthermore, lysosomal degradation of activated epidermal growth factor receptor was dramatically impaired in small inhibitory RNA-treated cells. We demonstrate that phosphatidylinositol 4-kinase IIalpha is necessary for the correct endocytic traffic and downregulation of activated epidermal growth factor receptor.

摘要

最近研究表明,磷脂酰肌醇4激酶IIα亚型在衔接蛋白-1复合物募集至反式高尔基体网络过程中发挥作用。在此,我们发现磷脂酰肌醇4激酶IIα也是内体系统高度动态膜的组成成分,它与晚期内体的蛋白质标记物以及内吞的表皮生长因子共定位。当使用单克隆抗体4C5G在体内抑制磷脂酰肌醇4激酶IIα活性,或通过RNA干扰降低内源性磷脂酰肌醇4激酶IIα蛋白水平时,与配体结合的表皮生长因子受体无法转运至晚期内体,而是在质膜下区室的囊泡中积累。此外,在经小干扰RNA处理的细胞中,活化的表皮生长因子受体的溶酶体降解显著受损。我们证明,磷脂酰肌醇4激酶IIα对于活化的表皮生长因子受体的正确内吞运输和下调是必需的。

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