Coly Pierre-Michaël, Gandolfo Pierrick, Castel Hélène, Morin Fabrice
Normandie Univ, UNIROUEN, Institut National de la Santé et de la Recherche Médicale (INSERM), DC2NRouen, France; Institute for Research and Innovation in BiomedicineRouen, France.
Front Neurosci. 2017 Feb 16;11:78. doi: 10.3389/fnins.2017.00078. eCollection 2017.
Autophagy is a highly conserved self-degradative process that plays a key role in diverse cellular processes such as stress response or differentiation. A growing body of work highlights the direct involvement of autophagy in cell migration and cancer metastasis. Specifically, autophagy has been shown to be involved in modulating cell adhesion dynamics as well as epithelial-to-mesenchymal transition. After providing a general overview of the mechanisms controlling autophagosome biogenesis and cell migration, we discuss how chemotactic G protein-coupled receptors, through the repression of autophagy, may orchestrate membrane trafficking and compartmentation of specific proteins at the cell front in order to support the critical steps of directional migration.
自噬是一种高度保守的自我降解过程,在应激反应或分化等多种细胞过程中起关键作用。越来越多的研究工作强调了自噬直接参与细胞迁移和癌症转移。具体而言,自噬已被证明参与调节细胞黏附动力学以及上皮-间质转化。在对控制自噬体生物发生和细胞迁移的机制进行总体概述后,我们将讨论趋化性G蛋白偶联受体如何通过抑制自噬来协调膜运输以及特定蛋白质在细胞前端的区室化,以支持定向迁移的关键步骤。