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线粒体相关内质网膜:与自噬过程密不可分。

Mitochondria-Associated Endoplasmic Reticulum Membranes: Inextricably Linked with Autophagy Process.

机构信息

Department of Implantology, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University, Jinan, China.

Shandong Key Laboratory of Oral Tissue Regeneration, Jinan, China.

出版信息

Oxid Med Cell Longev. 2022 Aug 23;2022:7086807. doi: 10.1155/2022/7086807. eCollection 2022.

DOI:10.1155/2022/7086807
PMID:36052160
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9427242/
Abstract

Mitochondria-associated membranes (MAMs), physical connection sites between the endoplasmic reticulum (ER) and the outer mitochondrial membrane (OMM), are involved in numerous cellular processes, such as calcium ion transport, lipid metabolism, autophagy, ER stress, mitochondria morphology, and apoptosis. Autophagy is a highly conserved intracellular process in which cellular contents are delivered by double-membrane vesicles, called autophagosomes, to the lysosomes for destruction and recycling. Autophagy, typically triggered by stress, eliminates damaged or redundant protein molecules and organelles to maintain regular cellular activity. Dysfunction of MAMs or autophagy is intimately associated with various diseases, including aging, cardiovascular, infections, cancer, multiple toxic agents, and some genetic disorders. Increasing evidence has shown that MAMs play a significant role in autophagy development and maturation. In our study, we concentrated on two opposing functions of MAMs in autophagy: facilitating the formation of autophagosomes and inhibiting autophagy. We recognized the link between MAMs and autophagy in the occurrence and progression of the diseases and therefore collated and summarized the existing intrinsic molecular mechanisms. Furthermore, we draw attention to several crucial data and open issues in the area that may be helpful for further study.

摘要

线粒体相关膜(MAMs),内质网(ER)和外线粒体膜(OMM)之间的物理连接位点,参与许多细胞过程,如钙离子运输、脂质代谢、自噬、ER 应激、线粒体形态和细胞凋亡。自噬是一种高度保守的细胞内过程,其中细胞内容物通过双层膜囊泡(称为自噬体)递送至溶酶体进行破坏和再循环。自噬通常由应激引发,消除受损或多余的蛋白质分子和细胞器,以维持正常的细胞活动。MAMs 或自噬的功能障碍与各种疾病密切相关,包括衰老、心血管疾病、感染、癌症、多种毒性物质和一些遗传疾病。越来越多的证据表明,MAMs 在自噬的发展和成熟中起着重要作用。在我们的研究中,我们集中研究了 MAMs 在自噬中的两个相反的功能:促进自噬体的形成和抑制自噬。我们认识到 MAMs 和自噬在疾病发生和发展中的联系,并因此整理和总结了现有的内在分子机制。此外,我们还提请注意该领域的几个关键数据和悬而未决的问题,这可能有助于进一步的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f8/9427242/4bc5659699c0/OMCL2022-7086807.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f8/9427242/6fa9d515738a/OMCL2022-7086807.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f8/9427242/f45d9e41fbf3/OMCL2022-7086807.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f8/9427242/17332db68623/OMCL2022-7086807.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f8/9427242/4bc5659699c0/OMCL2022-7086807.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f8/9427242/6fa9d515738a/OMCL2022-7086807.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f8/9427242/f45d9e41fbf3/OMCL2022-7086807.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f8/9427242/17332db68623/OMCL2022-7086807.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f8/9427242/4bc5659699c0/OMCL2022-7086807.004.jpg

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