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动力相关蛋白1、裂变与凋亡

DRP1, fission and apoptosis.

作者信息

Wang Nan, Wang Xinwai, Lan Beiwu, Gao Yufei, Cai Yuanyuan

机构信息

The Department of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun, China.

The First Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun, China.

出版信息

Cell Death Discov. 2025 Apr 7;11(1):150. doi: 10.1038/s41420-025-02458-0.

DOI:10.1038/s41420-025-02458-0
PMID:40195359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11977278/
Abstract

Mitochondrial fission is a critical physiological process in eukaryotic cells, participating in various vital activities such as mitosis, mitochondria quality control, and mitophagy. Recent studies have revealed a tight connection between mitochondrial fission and the mitochondrial metabolism, as well as apoptosis, which involves multiple cellular events and interactions between organelles. As a pivotal molecule in the process of mitochondrial fission, the function of DRP1 is regulated at multiple levels, including transcription, post-translational modifications. This review follows the guidelines for Human Gene Nomenclature and will focus on DRP1, discussing its activity regulation, its role in mitochondrial fission, and the relationship between mitochondrial fission and apoptosis.

摘要

线粒体分裂是真核细胞中的一个关键生理过程,参与有丝分裂、线粒体质量控制和线粒体自噬等各种重要活动。最近的研究揭示了线粒体分裂与线粒体代谢以及细胞凋亡之间的紧密联系,细胞凋亡涉及多个细胞事件和细胞器之间的相互作用。作为线粒体分裂过程中的一个关键分子,动力相关蛋白1(DRP1)的功能在多个水平受到调控,包括转录、翻译后修饰。本综述遵循人类基因命名法指南,将聚焦于DRP1,讨论其活性调节、在 mitochondrial fission 中的作用以及线粒体分裂与细胞凋亡之间的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dca3/11977278/06d2982f3a8f/41420_2025_2458_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dca3/11977278/e803d3cb7d7e/41420_2025_2458_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dca3/11977278/06d2982f3a8f/41420_2025_2458_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dca3/11977278/e803d3cb7d7e/41420_2025_2458_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dca3/11977278/06d2982f3a8f/41420_2025_2458_Fig2_HTML.jpg

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Cerebellum. 2024 Oct;23(5):2042-2049. doi: 10.1007/s12311-024-01701-1. Epub 2024 May 13.
2
Cdk8/CDK19 promotes mitochondrial fission through Drp1 phosphorylation and can phenotypically suppress pink1 deficiency in Drosophila.Cdk8/CDK19 通过磷酸化 Drp1 促进线粒体裂变,并在果蝇中表型上抑制 pink1 缺失。
Nat Commun. 2024 Apr 18;15(1):3326. doi: 10.1038/s41467-024-47623-8.
3
Mitochondria act as a key regulatory factor in cancer progression: Current concepts on mutations, mitochondrial dynamics, and therapeutic approach.
线粒体在癌症进展中充当关键调节因子:突变、线粒体动力学和治疗方法的当前概念。
Mutat Res Rev Mutat Res. 2024 Jan-Jun;793:108490. doi: 10.1016/j.mrrev.2024.108490. Epub 2024 Mar 8.
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Targeting mitochondrial dynamics and redox regulation in cardiovascular diseases.靶向心血管疾病中线粒体动态和氧化还原调节。
Trends Pharmacol Sci. 2024 Apr;45(4):290-303. doi: 10.1016/j.tips.2024.02.001. Epub 2024 Mar 7.
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Drp1: Focus on Diseases Triggered by the Mitochondrial Pathway.DRP1:关注由线粒体途径引发的疾病。
Cell Biochem Biophys. 2024 Jun;82(2):435-455. doi: 10.1007/s12013-024-01245-5. Epub 2024 Mar 4.
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The interplay between mitochondrial dynamics and autophagy: From a key homeostatic mechanism to a driver of pathology.线粒体动力学与自噬的相互作用:从关键的动态平衡机制到病理的驱动因素。
Semin Cell Dev Biol. 2024 Sep-Oct;161-162:1-19. doi: 10.1016/j.semcdb.2024.02.001. Epub 2024 Mar 1.
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Mitochondria in disease: changes in shapes and dynamics.线粒体在疾病中的作用:形态和动力学的变化。
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