Literature DB >> 29257951

Atg5 Disassociates the V1V0-ATPase to Promote Exosome Production and Tumor Metastasis Independent of Canonical Macroautophagy.

Huishan Guo1, Maneka Chitiprolu1, Luc Roncevic1, Charlotte Javalet2, Fiona J Hemming2, My Tran Trung1, Lingrui Meng1, Elyse Latreille1, Christiano Tanese de Souza3, Danielle McCulloch1, R Mitchell Baldwin1, Rebecca Auer3, Jocelyn Côté1, Ryan Charles Russell1, Rémy Sadoul2, Derrick Gibbings4.   

Abstract

Autophagy and autophagy-related genes (Atg) have been attributed prominent roles in tumorigenesis, tumor growth, and metastasis. Extracellular vesicles called exosomes are also implicated in cancer metastasis. Here, we demonstrate that exosome production is strongly reduced in cells lacking Atg5 and Atg16L1, but this is independent of Atg7 and canonical autophagy. Atg5 specifically decreases acidification of late endosomes where exosomes are produced, disrupting the acidifying V1V0-ATPase by removing a regulatory component, ATP6V1E1, into exosomes. The effect of Atg5 on exosome production promotes the migration and in vivo metastasis of orthotopic breast cancer cells. These findings uncover mechanisms controlling exosome release and identify means by which autophagy-related genes can contribute to metastasis in autophagy-independent pathways.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  LC3; V(1)V(0)-ATPase; acidification; autophagy; cancer; endosome; exosomes; extracellular vesicles; multivesicular body; tumor

Mesh:

Substances:

Year:  2017        PMID: 29257951     DOI: 10.1016/j.devcel.2017.11.018

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


  76 in total

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