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由ARF6和Rab11调控的整合素β1的刺激依赖性再循环

Stimulation-dependent recycling of integrin beta1 regulated by ARF6 and Rab11.

作者信息

Powelka Aimee M, Sun Jianlan, Li Jian, Gao Minggeng, Shaw Leslie M, Sonnenberg Arnoud, Hsu Victor W

机构信息

Brigham and Women's Hospital, and Department of Medicine, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Traffic. 2004 Jan;5(1):20-36. doi: 10.1111/j.1600-0854.2004.00150.x.

Abstract

In comparison to the internalization pathways of endocytosis, the recycling pathways are less understood. Even less defined is the process of regulated recycling, as few examples exist and their underlying mechanisms remain to be clarified. In this study, we examine the endocytic recycling of integrin beta1, a process that has been suggested to play an important role during cell motility by mediating the redistribution of integrins to the migrating front. External stimulation regulates the endocytic itinerary of beta1, mainly at an internal compartment that is likely to be a subset of the recycling endosomes. This stimulation-dependent recycling is regulated by ARF6 and Rab11, and also requires the actin cytoskeleton in an ARF6-dependent manner. Consistent with these observations being relevant for cell motility, mutant forms of ARF6 that affect either actin rearrangement or recycling inhibit the motility of a breast cancer cell line.

摘要

与内吞作用的内化途径相比,回收途径的了解较少。调节性回收过程的定义甚至更少,因为实例很少,其潜在机制仍有待阐明。在本研究中,我们研究了整合素β1的内吞回收过程,该过程被认为通过介导整合素重新分布到迁移前沿在细胞运动中发挥重要作用。外部刺激主要在一个可能是回收内体子集的内部区室调节β1的内吞行程。这种依赖刺激的回收由ARF6和Rab11调节,并且还以ARF6依赖的方式需要肌动蛋白细胞骨架。与这些观察结果与细胞运动相关一致,影响肌动蛋白重排或回收的ARF6突变形式会抑制乳腺癌细胞系的运动。

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