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Mitocytosis, a migrasome-mediated mitochondrial quality-control process
Abstract
Damaged mitochondria need to be cleared to maintain the quality of the mitochondrial pool. Here, we report mitocytosis, a migrasome-mediated mitochondrial quality-control process. We found that, upon exposure to mild mitochondrial stresses, damaged mitochondria are transported into migrasomes and subsequently disposed of from migrating cells. Mechanistically, mitocytosis requires positioning of damaged mitochondria at the cell periphery, which occurs because damaged mitochondria avoid binding to inward motor proteins. Functionally, mitocytosis plays an important role in maintaining mitochondrial quality. Enhanced mitocytosis protects cells from mitochondrial stressor-induced loss of mitochondrial membrane potential (MMP) and mitochondrial respiration; conversely, blocking mitocytosis causes loss of MMP and mitochondrial respiration under normal conditions. Physiologically, we demonstrate that mitocytosis is required for maintaining MMP and viability in neutrophils in vivo. We propose that mitocytosis is an important mitochondrial quality-control process in migrating cells, which couples mitochondrial homeostasis with cell migration.
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“For example, a recent study demonstrated that Myo19 binds and tethers damaged mitochondria to actin for removal through a process termed mitocytosis [67].”
From Nascent RHOH acts as a molecular brake on actomyosin-mediated effector functions of inflammatory neutrophils (2022) · cites this paper as [67]
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Mitochondrial degradation: Mitophagy and beyond
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Transmembrane proteins tetraspanin 4 and CD9 sense membrane curvature
Dharan, R., Goren, S., Cheppali, S. K., Shendrik, P., Brand, G., Vaknin, A., Yu, L., Kozlov, M. M., & Sorkin, R. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2208993119 · Cited by 70
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Molecular Regulation and Oncogenic Functions of TSPAN8
Yang, J., Zhang, Z., Lam, J. S. W., Fan, H., & Fu, N. Y. (2024) · Cells · doi:10.3390/cells13020193 · Cited by 11
Metadata
- Authors
- Jiao, H., Jiang, D., Hu, X., Du, W., Ji, L., Yang, Y., Li, X., Sho, T., Wang, X., Li, Y., Wu, Y.-T., Wei, Y.-H., Hu, X., & Yu, L.
- ORCID
- Yang, Yuzhuo
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2021-05
- Volume
- 184
- Issue
- 11
- Pages
- 2896-2910.e13
- ISSN
- 0092-8674
- Cited by
- 570
- References
- 8
- Language
- en
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 391 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Funders
- Ministry of Science and Technology of the People's Republic of China
- National Natural Science Foundation of China
- Beijing Municipal Science and Technology Commission
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