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自噬在细胞膜运输系统中的作用:Atg9 囊泡之谜。

Autophagy in the context of the cellular membrane-trafficking system: the enigma of Atg9 vesicles.

机构信息

Center for Frontier Oral Science, Graduate School of Dentistry, Osaka University, Osaka 565-0871, Japan

出版信息

Biochem Soc Trans. 2017 Dec 15;45(6):1323-1331. doi: 10.1042/BST20170128. Epub 2017 Nov 17.

DOI:10.1042/BST20170128
PMID:29150528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5730941/
Abstract

Macroautophagy is an intracellular degradation system that involves the formation of membrane structures called autophagosomes, although the detailed process by which membrane lipids are supplied during autophagosome formation is yet to be elucidated. Macroautophagy is thought to be associated with canonical membrane trafficking, but several mechanistic details are still missing. In this review, the current understanding and potential mechanisms by which membrane trafficking participates in macroautophagy are described, with a focus on the enigma of the membrane protein Atg9, for which the proximal mechanisms determining its movement are disputable, despite its key role in autophagosome formation.

摘要

自噬是一种细胞内降解系统,涉及膜结构的形成,称为自噬体,尽管自噬体形成过程中膜脂质的供应的详细过程尚未阐明。自噬被认为与经典的膜运输有关,但仍有几个机制细节缺失。在这篇综述中,描述了膜运输参与自噬的当前理解和潜在机制,重点介绍了膜蛋白 Atg9 的谜团,尽管其在自噬体形成中起着关键作用,但决定其运动的近端机制仍存在争议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94dc/5730941/8a6f4c77ad93/BST-45-1323-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94dc/5730941/6ef8f517369b/BST-45-1323-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94dc/5730941/8a92062e6462/BST-45-1323-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94dc/5730941/fc616f67d9fb/BST-45-1323-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94dc/5730941/8a6f4c77ad93/BST-45-1323-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94dc/5730941/6ef8f517369b/BST-45-1323-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94dc/5730941/8a92062e6462/BST-45-1323-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94dc/5730941/fc616f67d9fb/BST-45-1323-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94dc/5730941/8a6f4c77ad93/BST-45-1323-g0004.jpg

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Regulation of Autophagy through TORC1 and mTORC1.通过TORC1和mTORC1对自噬的调控
Biomolecules. 2017 Jul 7;7(3):52. doi: 10.3390/biom7030052.
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The Arl3 and Arl1 GTPases co-operate with Cog8 to regulate selective autophagy via Atg9 trafficking.Arl3 和 Arl1 GTPases 与 Cog8 合作,通过 Atg9 运输来调节选择性自噬。
ATG9/ATG9A 在自噬中的新兴作用:对细胞和神经生物学的影响。
Autophagy. 2024 Nov;20(11):2373-2387. doi: 10.1080/15548627.2024.2384349. Epub 2024 Aug 4.
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Drug discovery by targeting the protein-protein interactions involved in autophagy.通过靶向自噬过程中涉及的蛋白质-蛋白质相互作用来进行药物发现。
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Autophagy in hepatic ischemia-reperfusion injury.肝脏缺血再灌注损伤中的自噬
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