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Impaired mitochondrial-endoplasmic reticulum interaction and mitophagy in Miro1-mutant neurons in Parkinson's disease.帕金森病中 Miro1 突变神经元中线粒体-内质网相互作用和线粒体自噬受损。
Hum Mol Genet. 2020 May 28;29(8):1353-1364. doi: 10.1093/hmg/ddaa066.
2
Posttranslational Modifications Mediate the Structural Diversity of Tauopathy Strains.翻译后修饰介导了tau蛋白病毒株的结构多样性。
Cell. 2020 Feb 20;180(4):633-644.e12. doi: 10.1016/j.cell.2020.01.027. Epub 2020 Feb 6.
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Variants in Miro1 Cause Alterations of ER-Mitochondria Contact Sites in Fibroblasts from Parkinson's Disease Patients.Miro1基因变异导致帕金森病患者成纤维细胞内质网-线粒体接触位点改变。
J Clin Med. 2019 Dec 16;8(12):2226. doi: 10.3390/jcm8122226.
4
LRRK2 regulates endoplasmic reticulum-mitochondrial tethering through the PERK-mediated ubiquitination pathway.LRRK2 通过 PERK 介导的泛素化途径调节内质网-线粒体连接。
EMBO J. 2020 Jan 15;39(2):e100875. doi: 10.15252/embj.2018100875. Epub 2019 Dec 10.
5
MERLIN: a novel BRET-based proximity biosensor for studying mitochondria-ER contact sites.MERLIN:一种新型基于 BRET 的临近生物传感器,用于研究线粒体-内质网接触位点。
Life Sci Alliance. 2019 Dec 9;3(1). doi: 10.26508/lsa.201900600. Print 2020 Jan.
6
DJ-1 regulates the integrity and function of ER-mitochondria association through interaction with IP3R3-Grp75-VDAC1.DJ-1 通过与 IP3R3-Grp75-VDAC1 的相互作用调节 ER-线粒体的完整性和功能。
Proc Natl Acad Sci U S A. 2019 Dec 10;116(50):25322-25328. doi: 10.1073/pnas.1906565116. Epub 2019 Nov 25.
7
Miro clusters regulate ER-mitochondria contact sites and link cristae organization to the mitochondrial transport machinery.Miro 簇调节内质网-线粒体接触位点,并将嵴的组织与线粒体运输机制联系起来。
Nat Commun. 2019 Sep 27;10(1):4399. doi: 10.1038/s41467-019-12382-4.
8
MITOL deletion in the brain impairs mitochondrial structure and ER tethering leading to oxidative stress.脑中线粒体缺失会损害线粒体结构和内质网的连接,导致氧化应激。
Life Sci Alliance. 2019 Aug 15;2(4). doi: 10.26508/lsa.201900308. Print 2019 Aug.
9
TOM40 Targets Atg2 to Mitochondria-Associated ER Membranes for Phagophore Expansion.TOM40 将 Atg2 靶向到与线粒体相关的内质网膜以促进吞噬体扩张。
Cell Rep. 2019 Aug 13;28(7):1744-1757.e5. doi: 10.1016/j.celrep.2019.07.036.
10
Mul1 restrains Parkin-mediated mitophagy in mature neurons by maintaining ER-mitochondrial contacts.Mul1 通过维持内质网-线粒体接触来抑制成熟神经元中 Parkin 介导的线粒体自噬。
Nat Commun. 2019 Aug 13;10(1):3645. doi: 10.1038/s41467-019-11636-5.

线粒体-内质网在神经退行性疾病中的连接

Mitochondria-ER Tethering in Neurodegenerative Diseases.

机构信息

Departamento de Genetica e Biologia Evolutiva, Instituto de Biociencias, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.

出版信息

Cell Mol Neurobiol. 2022 May;42(4):917-930. doi: 10.1007/s10571-020-01008-9. Epub 2020 Nov 16.

DOI:10.1007/s10571-020-01008-9
PMID:33196974
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11441217/
Abstract

Organelles juxtaposition has been detected for decades, although only recently gained importance due to a pivotal role in the regulation of cellular processes dependent on membrane contact sites. Endoplasmic reticulum (ER) and mitochondria interaction is a prime example of organelles contact sites. Mitochondria-associated membranes (MAM) are proposed to harbor ER-mitochondria tether complexes, mainly when these organelles are less than 30 nm apart. Dysfunctions of proteins located at the MAM are associated with neurodegenerative diseases such as Parkinson's, Alzheimer's and amyotrophic lateral sclerosis, as well as neurodevelopmental disorders; hence any malfunction in MAM can potentially trigger cell death. This review will focus on the role of ER-mitochondria contact sites, regarding calcium homeostasis, lipid metabolism, autophagy, morphology and dynamics of mitochondria, mainly in the context of neurodegenerative diseases. Approaches that have been employed so far to study organelles contact sites, as well as methods that were not used in neurosciences yet, but are promising and accurate ways to unveil the functions of MAM during neurodegeneration, is also discussed in the present review.

摘要

几十年来,人们一直检测到细胞器的并列排列,尽管直到最近,由于它们在依赖膜接触位点的细胞过程调节中起着关键作用,才引起了人们的重视。内质网 (ER) 和线粒体的相互作用就是细胞器接触位点的一个主要例子。有人提出,线粒体相关膜 (MAM) 含有 ER-线粒体系绳复合物,主要是当这些细胞器之间的距离小于 30nm 时。位于 MAM 的蛋白质的功能障碍与神经退行性疾病如帕金森病、阿尔茨海默病和肌萎缩侧索硬化症以及神经发育障碍有关;因此,MAM 的任何功能障碍都可能引发细胞死亡。本综述将重点关注 ER-线粒体接触位点在钙动态平衡、脂质代谢、自噬、线粒体形态和动力学方面的作用,主要是在神经退行性疾病的背景下。本文还讨论了迄今为止用于研究细胞器接触位点的方法,以及尚未在神经科学中使用但具有很大应用前景的方法,这些方法是揭示神经退行性变过程中 MAM 功能的准确方法。