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DGAT1-Dependent Lipid Droplet Biogenesis Protects Mitochondrial Function during Starvation-Induced Autophagy.依赖二酰甘油酰基转移酶1的脂滴生物合成在饥饿诱导的自噬过程中保护线粒体功能。
Dev Cell. 2017 Jul 10;42(1):9-21.e5. doi: 10.1016/j.devcel.2017.06.003.
2
Phosphorylation of the mitochondrial autophagy receptor Nix enhances its interaction with LC3 proteins.线粒体自噬受体 Nix 的磷酸化增强了它与 LC3 蛋白的相互作用。
Sci Rep. 2017 Apr 25;7(1):1131. doi: 10.1038/s41598-017-01258-6.
3
Drp1-dependent mitophagy protects against cisplatin-induced apoptosis of renal tubular epithelial cells by improving mitochondrial function.依赖动力相关蛋白1(Drp1)的线粒体自噬通过改善线粒体功能来保护肾小管上皮细胞免受顺铂诱导的细胞凋亡。
Oncotarget. 2017 Mar 28;8(13):20988-21000. doi: 10.18632/oncotarget.15470.
4
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Autophagy. 2017 Jun 3;13(6):1080-1081. doi: 10.1080/15548627.2017.1300224. Epub 2017 Mar 21.
5
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Mitochondrial E3 ligase MARCH5 regulates FUNDC1 to fine-tune hypoxic mitophagy.线粒体E3连接酶MARCH5调节FUNDC1以微调低氧线粒体自噬。
EMBO Rep. 2017 Mar;18(3):495-509. doi: 10.15252/embr.201643309. Epub 2017 Jan 19.
7
The pharmacological regulation of cellular mitophagy.细胞线粒体自噬的药理学调控。
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New methods for monitoring mitochondrial biogenesis and mitophagy in vitro and in vivo.体外和体内监测线粒体生物发生和线粒体自噬的新方法。
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The mitochondria-targeted antioxidant MitoQ ameliorated tubular injury mediated by mitophagy in diabetic kidney disease via Nrf2/PINK1.线粒体靶向抗氧化剂MitoQ通过Nrf2/PINK1改善糖尿病肾病中由线粒体自噬介导的肾小管损伤。
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线粒体自噬的机制、病理生理作用及分析方法——最新见解

Mechanisms, pathophysiological roles and methods for analyzing mitophagy - recent insights.

作者信息

Williams Jessica A, Ding Wen-Xing

机构信息

Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, 3901 Rainbow Blvd., Kansas City, KS 66160, USA.

Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, KS 66160, USA.

出版信息

Biol Chem. 2018 Jan 26;399(2):147-178. doi: 10.1515/hsz-2017-0228.

DOI:10.1515/hsz-2017-0228
PMID:28976892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5835338/
Abstract

In 2012, we briefly summarized the mechanisms, pathophysiological roles and methods for analyzing mitophagy. As then, the mitophagy field has continued to grow rapidly, and many new molecular mechanisms regulating mitophagy and molecular tools for monitoring mitophagy have been discovered and developed. Therefore, the purpose of this review is to update information regarding these advances in mitophagy while focusing on basic molecular mechanisms of mitophagy in different organisms and its pathophysiological roles. We also discuss the advantage and limitations of current methods to monitor and quantify mitophagy in cultured cells and in vivo mouse tissues.

摘要

2012年,我们简要总结了线粒体自噬的机制、病理生理作用及分析方法。自那时起,线粒体自噬领域持续快速发展,发现并开发了许多调控线粒体自噬的新分子机制以及监测线粒体自噬的分子工具。因此,本综述的目的是更新线粒体自噬方面的这些进展,同时聚焦于不同生物体中线粒体自噬的基本分子机制及其病理生理作用。我们还讨论了当前用于监测和量化培养细胞及体内小鼠组织中线粒体自噬的方法的优缺点。