Mitochondrial‐derived vesicles retain membrane potential and contain a functional ATP synthase

Author:

Hazan (Ben‐Menachem) Reut1,Lintzer Dvora1,Ziv Tamar2ORCID,Das Koyeli1ORCID,Rosenhek‐Goldian Irit3ORCID,Porat Ziv4,Ben Ami Pilo Hila5,Karniely Sharon6ORCID,Saada Ann7ORCID,Regev‐Rudzki Neta5ORCID,Pines Ophry1ORCID

Affiliation:

1. Department of Molecular Genetics and Microbiology, IMRIC, Faculty of Medicine Hebrew University Jerusalem Israel

2. Smoler Proteomics Center, Technion Haifa Israel

3. Departments of Chemical Research Support Weizmann Institute of Science Rehovot Israel

4. Flow Cytometry Unit, Department of Life Sciences Core Facilities Weizmann Institute of Science Rehovot Israel

5. Department of Biomolecular Sciences Weizmann Institute of Science Rehovot Israel

6. Division of Virology Kimron Veterinary Institute Bet Dagan Israel

7. Department of Genetics, Hadassah Medical Center and Faculty of Medicine Hebrew University Jerusalem Israel

Abstract

AbstractVesicular transport is a means of communication. While cells can communicate with each other via secretion of extracellular vesicles, less is known regarding organelle‐to organelle communication, particularly in the case of mitochondria. Mitochondria are responsible for the production of energy and for essential metabolic pathways in the cell, as well as fundamental processes such as apoptosis and aging. Here, we show that functional mitochondria isolated from Saccharomyces cerevisiae release vesicles, independent of the fission machinery. We isolate these mitochondrial‐derived vesicles (MDVs) and find that they are relatively uniform in size, of about 100 nm, and carry selective protein cargo enriched for ATP synthase subunits. Remarkably, we further find that these MDVs harbor a functional ATP synthase complex. We demonstrate that these vesicles have a membrane potential, produce ATP, and seem to fuse with naive mitochondria. Our findings reveal a possible delivery mechanism of ATP‐producing vesicles, which can potentially regenerate ATP‐deficient mitochondria and may participate in organelle‐to‐organelle communication.

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Biochemistry

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3