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MITOL/MARCHF5 通过泛素介导的线粒体调节一目了然。

Ubiquitin-mediated mitochondrial regulation by MITOL/MARCHF5 at a glance.

机构信息

Laboratory of Regenerative Medicine, School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo 192-0392, Japan.

Laboratory of Molecular Biochemistry, Department of Life Science, Faculty of Science, Gakushuin University, Toshima, Tokyo 171-8588, Japan.

出版信息

J Biochem. 2022 Dec 27;173(1):1-11. doi: 10.1093/jb/mvac092.

Abstract

Mitochondria are involved in various cellular processes, such as energy production, inflammatory responses and cell death. Mitochondrial dysfunction is associated with many age-related diseases, including neurological disorders and heart failure. Mitochondrial quality is strictly maintained by mitochondrial dynamics linked to an adequate supply of phospholipids and other substances from the endoplasmic reticulum (ER). The outer mitochondrial membrane-localized E3 ubiquitin ligase MITOL/MARCHF5 is responsible for mitochondrial quality control through the regulation of mitochondrial dynamics, formation of mitochondria-ER contacts and mitophagy. MITOL deficiency has been shown to impair mitochondrial function, cause an excessive inflammatory response and increase vulnerability to stress, resulting in the exacerbation of the disease. In this study, we overview the ubiquitin-mediated regulation of mitochondrial function by MITOL and the relationship between MITOL and diseases.

摘要

线粒体参与多种细胞过程,如能量产生、炎症反应和细胞死亡。线粒体功能障碍与许多与年龄相关的疾病有关,包括神经紊乱和心力衰竭。线粒体的质量通过与内质网(ER)充足供应磷脂和其他物质相关的线粒体动力学来严格维持。定位于线粒体外膜的 E3 泛素连接酶 MITOL/MARCHF5 通过调节线粒体动力学、形成线粒体-内质网接触和线粒体自噬来负责线粒体质量控制。MITOL 缺乏已被证明会损害线粒体功能,引起过度的炎症反应,并增加对压力的脆弱性,从而导致疾病恶化。在这项研究中,我们概述了 MITOL 介导的线粒体功能的泛素调节以及 MITOL 与疾病之间的关系。

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