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线粒体衍生小泡:最新见解。

Mitochondrial-derived vesicles: Recent insights.

机构信息

"Nicolae Simionescu" Institute of Cellular Biology and Pathology of the Romanian Academy, Bucharest, Romania.

出版信息

J Cell Mol Med. 2022 Jun;26(12):3323-3328. doi: 10.1111/jcmm.17391. Epub 2022 May 18.

DOI:10.1111/jcmm.17391
PMID:35582908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9189329/
Abstract

The generation of vesicles is a constitutive attribute of mitochondria inherited from bacterial ancestors. The physiological conditions and mild oxidative stress promote oxidation and dysfunction of certain proteins and lipids within the mitochondrial membranes; these constituents are subsequently packed as small mitochondrial-derived vesicles (MDVs) (70-150 nm in diameter) and are transported intracellularly to lysosomes and peroxisomes to be degraded. In this way, MDVs remove the damaged mitochondrial components, preserve mitochondrial structural and functional integrity and restore homeostasis. An outline of the current knowledge on MDVs seems to be necessary for understanding the potential impact of this research area in cellular (patho)physiology. The present synopsis is an attempt towards the accomplishment of this demand, highlighting also the still unclear issues related to MDVs. Here, we discuss (i) MDVs budding and generation (molecules and mechanisms), (ii) the distinct cargoes packed and transported by MDVs, (iii) the MDVs trafficking pathways and (iv) the biological role of MDVs, from quality controllers to the involvement in organellar crosstalk, mitochondrial antigen presentation and peroxisome de novo biogenesis. These complex roles uncover also mitochondria integration into the cellular environment. As the therapeutic exploitation of MDVs is currently limited, future insights into MDVs cell biology are expected to direct to novel diagnostic tools and treatments.

摘要

小泡的产生是线粒体的一个固有属性,它源自细菌祖先。生理条件和轻度氧化应激会促进线粒体膜内某些蛋白质和脂质的氧化和功能障碍;这些成分随后被包装成小的线粒体衍生小泡(MDV)(直径 70-150nm),并在细胞内被运输到溶酶体和过氧化物酶体中进行降解。通过这种方式,MDV 去除受损的线粒体成分,保持线粒体结构和功能的完整性,并恢复体内平衡。概述 MDV 的现有知识似乎对于理解该研究领域在细胞(病理)生理学中的潜在影响是必要的。本综述试图满足这一需求,同时还强调了与 MDV 相关的仍不清楚的问题。在这里,我们讨论了(i)MDV 的出芽和产生(分子和机制),(ii)MDV 包装和运输的不同货物,(iii)MDV 的运输途径以及(iv)MDV 的生物学作用,从质量控制器到参与细胞器串扰、线粒体抗原呈递和过氧化物酶体从头生物发生。这些复杂的作用也揭示了线粒体与细胞环境的整合。由于目前对 MDV 的治疗利用有限,对 MDV 细胞生物学的未来研究有望为新的诊断工具和治疗方法提供指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce4c/9189329/c4c03bf5b11f/JCMM-26-3323-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce4c/9189329/c4c03bf5b11f/JCMM-26-3323-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce4c/9189329/c4c03bf5b11f/JCMM-26-3323-g001.jpg

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Parkin beyond Parkinson's Disease-A Functional Meaning of Parkin Downregulation in TDP-43 Proteinopathies.
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