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本文引用的文献

1
Lysosomes drive the piecemeal removal of mitochondrial inner membrane.溶酶体驱动线粒体内膜的逐步去除。
Nature. 2024 Aug;632(8027):1110-1117. doi: 10.1038/s41586-024-07835-w. Epub 2024 Aug 21.
2
Perspectives of mitochondria-lysosome-related organelle in hepatocyte dedifferentiation and implications in chronic liver disease.线粒体-溶酶体相关细胞器在肝细胞去分化中的作用及对慢性肝病的影响
eGastroenterology. 2024 Jan;2(1). doi: 10.1136/egastro-2023-100046.
3
Mitochondria-lysosome-related organelles mediate mitochondrial clearance during cellular dedifferentiation.线粒体-溶酶体相关细胞器在细胞去分化过程中介导线粒体清除。
Cell Rep. 2023 Oct 31;42(10):113291. doi: 10.1016/j.celrep.2023.113291. Epub 2023 Oct 19.
4
A degradative to secretory autophagy switch mediates mitochondria clearance in the absence of the mATG8-conjugation machinery.一种降解到分泌自噬的转换在没有 mATG8 缀合机制的情况下介导线粒体清除。
Nat Commun. 2022 Jun 28;13(1):3720. doi: 10.1038/s41467-022-31213-7.
5
Mitocytosis, a migrasome-mediated mitochondrial quality-control process.有丝分裂,一种由迁移体介导的线粒体质量控制过程。
Cell. 2021 May 27;184(11):2896-2910.e13. doi: 10.1016/j.cell.2021.04.027.
6
Electron microscopic analysis of a spherical mitochondrial structure.电子显微镜分析球形线粒体结构。
J Biol Chem. 2012 Dec 7;287(50):42373-8. doi: 10.1074/jbc.M112.413674. Epub 2012 Oct 23.
7
Mitophagy: mechanisms, pathophysiological roles, and analysis.自噬:机制、病理生理作用及分析。
Biol Chem. 2012 Jul;393(7):547-64. doi: 10.1515/hsz-2012-0119.
8
A vesicular transport pathway shuttles cargo from mitochondria to lysosomes.囊泡运输途径将货物从线粒体运输到溶酶体。
Curr Biol. 2012 Jan 24;22(2):135-41. doi: 10.1016/j.cub.2011.11.057. Epub 2012 Jan 5.
9
Regulating mitochondrial outer membrane proteins by ubiquitination and proteasomal degradation.通过泛素化和蛋白酶体降解调节线粒体外膜蛋白。
Curr Opin Cell Biol. 2011 Aug;23(4):476-82. doi: 10.1016/j.ceb.2011.05.007. Epub 2011 Jun 24.
10
Membrane protein degradation by AAA proteases in mitochondria: extraction of substrates from either membrane surface.线粒体中AAA蛋白酶介导的膜蛋白降解:从任一膜表面提取底物
Mol Cell. 2000 Apr;5(4):629-38. doi: 10.1016/s1097-2765(00)80242-7.

线粒体的质量控制涉及溶酶体的多种明确方式。

Quality control of mitochondria involves lysosomes in multiple definitive ways.

机构信息

Faculty of Medical Sciences, Translational and Clinical Research Institute, Newcastle University, Newcastle Upon Tyne, UK.

Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, KS, USA.

出版信息

Autophagy. 2024 Dec;20(12):2599-2601. doi: 10.1080/15548627.2024.2408712. Epub 2024 Oct 6.

DOI:10.1080/15548627.2024.2408712
PMID:39324497
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11587833/
Abstract

Mitochondria are crucial organelles in maintaining cellular homeostasis. They are involved in processes such as energy production, metabolism of lipids and glucose, and cell death regulation. Mitochondrial dysfunction can lead to various health issues such as aging, cancer, neurodegenerative diseases, and chronic liver diseases. While mitophagy is the main process for getting rid of excess or damaged mitochondria, there are additional mechanisms for preserving mitochondrial quality. One such alternative mechanism we have discovered is a hybrid organelle called mitochondrial-lysosome-related-organelle (MLRO), which functions independently of the typical autophagy process. More recently, another type of vesicle called vesicle derived from the inner mitochondrial membrane (VDIM) has been identified to break down the inner mitochondrial membrane without involving the standard autophagy pathway. In this article, we will delve into the similarities and differences between MLRO and VDIM, including their structure, regulation, and relevance to human diseases.

摘要

线粒体是维持细胞内稳态的关键细胞器。它们参与能量产生、脂质和葡萄糖代谢以及细胞死亡调节等过程。线粒体功能障碍可导致各种健康问题,如衰老、癌症、神经退行性疾病和慢性肝病。虽然自噬是清除多余或受损线粒体的主要过程,但还有其他维持线粒体质量的机制。我们发现的一种这样的替代机制是一种称为线粒体-溶酶体相关细胞器(MLRO)的混合细胞器,它独立于典型的自噬过程发挥作用。最近,另一种称为源自线粒体内膜的囊泡(VDIM)的囊泡也被鉴定出来,它可以在不涉及标准自噬途径的情况下分解线粒体内膜。在本文中,我们将深入探讨 MLRO 和 VDIM 之间的相似之处和不同之处,包括它们的结构、调节以及与人类疾病的关系。