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ESCRT 介导线粒体自噬中噬体的封闭。

ESCRT-mediated phagophore sealing during mitophagy.

机构信息

Centre for Cancer Cell Reprogramming, Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Montebello, Norway.

Department of Molecular Cell Biology, Institute for Cancer Research, Oslo University Hospital, Montebello, Norway.

出版信息

Autophagy. 2020 May;16(5):826-841. doi: 10.1080/15548627.2019.1639301. Epub 2019 Aug 1.

Abstract

Inactivation of the endosomal sorting complex required for transport (ESCRT) machinery has been reported to cause autophagic defects, but the exact functions of ESCRT proteins in macroautophagy/autophagy remain incompletely understood. Using live-cell fluorescence microscopy we found that the filament-forming ESCRT-III subunit CHMP4B was recruited transiently to nascent autophagosomes during starvation-induced autophagy and mitophagy, with residence times of about 1 and 2 min, respectively. Correlative light microscopy and electron tomography revealed CHMP4B recruitment at a late step in mitophagosome formation. The autophagosomal dwell time of CHMP4B was strongly increased by depletion of the regulatory ESCRT-III subunit CHMP2A. Using a novel optogenetic closure assay we observed that depletion of CHMP2A inhibited phagophore sealing during mitophagy. Consistent with this, depletion of CHMP2A and other ESCRT-III subunits inhibited both PRKN/PARKIN-dependent and -independent mitophagy. We conclude that the ESCRT machinery mediates phagophore closure, and that this is essential for mitophagic flux. BSA: bovine serum albumin; CHMP: chromatin-modifying protein; CLEM: correlative light and electron microscopy; EGFP: enhanced green fluorescent protein; ESCRT: endosomal sorting complex required for transport; HEPES: 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid; HRP: horseradish peroxidase; ILV: intralumenal vesicle; MAP1LC3/LC3: microtubule-associated protein 1 light chain 3; LOV2: light oxygen voltage 2; MLS: mitochondrial localization sequence; MT-CO2: mitochondrially encoded cytochrome c oxidase II; O+A: oligomycin and antimycin A; PBS: phosphate-buffered saline; PIPES: piperazine-N,N-bis(2-ethanesulfonic acid); PRKN/PARKIN: parkin RBR E3 ubiquitin protein ligase; RAB: RAS-related in brain; SD: standard deviation; SEM: standard error of the mean; TOMM20: TOMM20: translocase of outer mitochondrial membrane 20; VCL: vinculin; VPS4: vacuolar protein sorting protein 4; Zdk1: Zdark 1; TUBG: Tubulin gamma chain.

摘要

已报道,对内体分选复合物必需的运输(ESCRT)机器的失活会导致自噬缺陷,但 ESCRT 蛋白在巨自噬/自噬中的确切功能仍不完全清楚。我们使用活细胞荧光显微镜发现,丝状 ESCRT-III 亚基 CHMP4B 在饥饿诱导的自噬和线粒体自噬过程中被短暂募集到新生自噬体上,停留时间分别约为 1 分钟和 2 分钟。相关的光显微镜和电子断层扫描显示 CHMP4B 在噬线粒体体形成的晚期被募集。CHMP2A 耗尽后,CHMP4B 在自噬体中的停留时间大大增加。使用新型光遗传学封闭测定法,我们观察到 CHMP2A 的耗竭抑制了线粒体自噬过程中的噬菌泡封闭。与此一致的是,CHMP2A 和其他 ESCRT-III 亚基的耗竭抑制了 PRKN/PARKIN 依赖性和非依赖性线粒体自噬。我们得出结论,ESCRT 机制介导噬菌泡闭合,这对于噬菌泡通量是必不可少的。BSA:牛血清白蛋白;CHMP:染色质修饰蛋白;CEM:光与电子显微镜相关;EGFp:增强型绿色荧光蛋白;ESCRT:内体分选复合物必需的运输;HEPES:2-[4-(2-羟乙基)哌嗪-1-基]乙磺酸;HRP:辣根过氧化物酶;ILV:腔内囊泡;MAP1LC3/LC3:微管相关蛋白 1 轻链 3;LOV2:光氧电压 2;MLS:线粒体定位序列;MT-CO2:线粒体编码细胞色素 c 氧化酶 II;O+A:寡霉素和抗霉素 A;PBS:磷酸盐缓冲盐水;PIPES:哌嗪-N,N-双(2-乙磺酸);PRKN/PARKIN:parkin RBR E3 泛素蛋白连接酶;RAB:脑中的 RAS 相关;SD:标准偏差;SEM:平均值的标准误差;TOMM20:TOMM20:外线粒体膜 20 转位酶;VCL: vinculin;VPS4:液泡蛋白分选蛋白 4;Zdk1:Zdark 1;TUBG:Tubulin gamma 链。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e210/7158923/d5885340497e/kaup-16-05-1639301-g001.jpg

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