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1
Defects of mitochondria-lysosomes communication induce secretion of mitochondria-derived vesicles and drive chemoresistance in ovarian cancer cells.线粒体-溶酶体通讯缺陷诱导线粒体衍生小泡的分泌并驱动卵巢癌细胞的化疗耐药性。
Cell Commun Signal. 2024 Mar 6;22(1):165. doi: 10.1186/s12964-024-01507-y.
2
Mitochondrial-derived vesicles in metabolism, disease, and aging.线粒体衍生小泡在代谢、疾病和衰老中的作用。
Cell Metab. 2024 Jan 2;36(1):21-35. doi: 10.1016/j.cmet.2023.11.014.
3
ALS-linked SOD1 mutations impair mitochondrial-derived vesicle formation and accelerate aging.与肌萎缩侧索硬化症相关的 SOD1 突变会损害线粒体衍生小泡的形成并加速衰老。
Redox Biol. 2024 Feb;69:102972. doi: 10.1016/j.redox.2023.102972. Epub 2023 Nov 24.
4
Mitochondrial-Derived Vesicles: The Good, the Bad, and the Ugly.线粒体衍生小泡:好、坏与丑。
Int J Mol Sci. 2023 Sep 8;24(18):13835. doi: 10.3390/ijms241813835.
5
Pleiotropic effects of mitochondria in aging.线粒体在衰老过程中的多效性作用。
Nat Aging. 2022 Mar;2(3):199-213. doi: 10.1038/s43587-022-00191-2. Epub 2022 Mar 17.
6
Mitochondrial-derived vesicles retain membrane potential and contain a functional ATP synthase.线粒体衍生小泡保留膜电位,并含有功能完整的 ATP 合酶。
EMBO Rep. 2023 May 4;24(5):e56114. doi: 10.15252/embr.202256114. Epub 2023 Mar 17.
7
Mitochondrial-Derived Vesicles-Link to Extracellular Vesicles and Implications in Cardiovascular Disease.线粒体衍生囊泡-连接细胞外囊泡及其在心血管疾病中的意义。
Int J Mol Sci. 2023 Jan 30;24(3):2637. doi: 10.3390/ijms24032637.
8
Mitochondrial-derived vesicles: Gatekeepers of mitochondrial response to oxidative stress.线粒体衍生小泡:线粒体应对氧化应激反应的守门员。
Free Radic Biol Med. 2022 Aug 1;188:185-193. doi: 10.1016/j.freeradbiomed.2022.06.233. Epub 2022 Jun 21.
9
Mitochondrial-derived vesicles: Recent insights.线粒体衍生小泡:最新见解。
J Cell Mol Med. 2022 Jun;26(12):3323-3328. doi: 10.1111/jcmm.17391. Epub 2022 May 18.
10
Cannabidiol activates PINK1-Parkin-dependent mitophagy and mitochondrial-derived vesicles.大麻二酚激活 PINK1-Parkin 依赖性线粒体自噬和线粒体衍生小泡。
Eur J Cell Biol. 2022 Jan;101(1):151185. doi: 10.1016/j.ejcb.2021.151185. Epub 2021 Nov 14.

线粒体衍生囊泡:为细胞动力源充电的潜在纳米电池。

Mitochondria-derived vesicles: potential nano-batteries to recharge the cellular powerhouse.

作者信息

Mishra Shalini, Deep Gagan

机构信息

Department of Internal Medicine-Gerontology and Geriatric Medicine, Wake Forest University School of Medicine, Winston-Salem, NC 27101, USA.

Sticht Center for Healthy Aging and Alzheimer's Prevention, Wake Forest University School of Medicine, Winston-Salem, NC 27101, USA.

出版信息

Extracell Vesicles Circ Nucl Acids. 2024 Jun;5(2):271-275. doi: 10.20517/evcna.2023.71. Epub 2024 Jun 10.

DOI:10.20517/evcna.2023.71
PMID:39092319
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11293460/
Abstract

Mitochondria dysfunction is increasingly recognized as a critical factor in various pathogenic processes. The mechanism governing mitochondrial quality control serves as an adaptive response, ensuring the preservation of mitochondrial morphology, quantity, and overall function, crucial for cell survival. The generation of mitochondria-derived vesicles (MDVs) is one of the processes of mitochondrial quality control. Recent literature has suggested MDV heterogeneity; however, the detailed characteristics of various MDV subtypes still need to be studied better. Recent studies have shown that MDVs also play a role in inter-organelle communication for mitochondria besides quality control. For instance, Hazan demonstrated that functional mitochondria from release vesicles independent of the fission machinery. These vesicles, falling within the typical size range of MDVs, were selectively loaded with mitochondrial proteins, especially with functional ATP synthase subunits. Intriguingly, these MDVs maintained membrane potential and could generate ATP. Moreover, MDVs could fuse with naïve mitochondria, transferring their ATP generation machinery. Lastly, this study revealed a potential delivery mechanism of ATP-producing vesicles, presenting a promising avenue to rejuvenate ATP-deficient mitochondria. Overall, this study unveils a novel mechanism for inter-organelle communication by vesicles, which is crucial for maintaining cellular homeostasis and could also be important in pathological conditions.

摘要

线粒体功能障碍日益被认为是各种致病过程中的关键因素。线粒体质量控制机制作为一种适应性反应,确保线粒体形态、数量和整体功能的维持,这对细胞存活至关重要。线粒体衍生囊泡(MDV)的产生是线粒体质量控制的过程之一。最近的文献表明MDV具有异质性;然而,各种MDV亚型的详细特征仍有待更深入研究。最近的研究表明,MDV除了在质量控制方面发挥作用外,还在线粒体的细胞器间通讯中发挥作用。例如,哈赞证明来自……的功能性线粒体释放独立于分裂机制的囊泡。这些囊泡在MDV的典型大小范围内,选择性地装载线粒体蛋白,特别是功能性ATP合酶亚基。有趣的是,这些MDV维持膜电位并能产生ATP。此外,MDV可以与未成熟的线粒体融合,转移其ATP生成机制。最后,这项研究揭示了产生ATP的囊泡的潜在传递机制,为使ATP缺乏的线粒体恢复活力提供了一条有前景的途径。总体而言,这项研究揭示了一种通过囊泡进行细胞器间通讯的新机制,这对维持细胞稳态至关重要,在病理条件下也可能很重要。