Hook1, microtubules, and Rab22: mediators of selective sorting of clathrin-independent endocytic cargo proteins on endosomes.

Bioarchitecture Pub Date : 2013-09-01 DOI:10.4161/bioa.26638
Lymarie Maldonado-Báez, Julie G Donaldson
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引用次数: 38

Abstract

Clathrin-independent endocytosis (CIE) mediates the internalization of many plasma membrane (PM) proteins involved in homeostasis, immune response, and signaling. CIE cargo molecules are internalized independent of clathrin, and dynamin, and modulated by the small G protein Arf6. After internalization the CIE cargo proteins either follow a default pathway of trafficking to lysosomes for degradation or follow a pathway where they are routed directly to the recycling endosomes for return to the PM. The selective endosomal sorting of molecules like CD44, CD98, and CD147, which are involved in cell-cell and cell-extracellular interactions, indicates that sorting mechanisms dictate the post-endocytic fate of CIE cargo proteins. In a recent study, we identified sorting signals that specify the endosomal trafficking of CIE cargo proteins and uncover a role for Hook1 as an endosomal cargo adaptor that routes CIE cargo to the recycling endosomes. Furthermore, we found that Hook1, microtubules, and Rab22a work in coordination to directly recycle the cargo and facilitate cell spreading. Here, we discuss our current view on the endosomal sorting of CIE cargo proteins and their molecular regulators.

Hook1、微管和Rab22:核内体上不依赖网格蛋白的内吞转运蛋白选择性分选的介质。
网格蛋白独立内吞作用(CIE)介导许多参与体内平衡、免疫反应和信号传导的质膜(PM)蛋白的内化。CIE货物分子的内化不依赖于网格蛋白和动力蛋白,由小G蛋白Arf6调节。内化后,CIE货物蛋白要么遵循运输到溶酶体降解的默认途径,要么遵循直接到达回收内体返回PM的途径。CD44、CD98和CD147等参与细胞间和细胞外相互作用的分子的选择性内体分选表明,分选机制决定了CIE货物蛋白的内吞后命运。在最近的一项研究中,我们确定了指定CIE货物蛋白内体运输的分类信号,并揭示了Hook1作为内体货物适配器的作用,该适配器将CIE货物运送到回收内体。此外,我们发现Hook1、微管和Rab22a协同工作,直接回收货物并促进细胞扩散。在这里,我们讨论了目前对CIE货物蛋白及其分子调节因子的内体分选的看法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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