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Mitochondrial dynamics involves molecular and mechanical events in motility, fusion and fission.

作者信息

Green Adam, Hossain Tanvir, Eckmann David M

机构信息

Department of Anesthesiology, The Ohio State University, Columbus, OH, United States.

Center for Medical and Engineering Innovation, The Ohio State University, Columbus, OH, United States.

出版信息

Front Cell Dev Biol. 2022 Oct 19;10:1010232. doi: 10.3389/fcell.2022.1010232. eCollection 2022.


DOI:10.3389/fcell.2022.1010232
PMID:36340034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9626967/
Abstract

Mitochondria are cell organelles that play pivotal roles in maintaining cell survival, cellular metabolic homeostasis, and cell death. Mitochondria are highly dynamic entities which undergo fusion and fission, and have been shown to be very motile in neurons and in multiple cell lines. Fusion and fission are essential for maintaining mitochondrial homeostasis through control of morphology, content exchange, inheritance of mitochondria, maintenance of mitochondrial DNA, and removal of damaged mitochondria by autophagy. Mitochondrial motility occurs through mechanical and molecular mechanisms which translocate mitochondria to sites of high energy demand. Motility also plays an important role in intracellular signaling. Here, we review key features that mediate mitochondrial dynamics and explore methods to advance the study of mitochondrial motility as well as mitochondrial dynamics-related diseases and mitochondrial-targeted therapeutics.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfad/9626967/c664fe518e84/fcell-10-1010232-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfad/9626967/5cbd1f932b71/fcell-10-1010232-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfad/9626967/98a3872e2d96/fcell-10-1010232-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfad/9626967/c664fe518e84/fcell-10-1010232-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfad/9626967/5cbd1f932b71/fcell-10-1010232-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfad/9626967/98a3872e2d96/fcell-10-1010232-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfad/9626967/c664fe518e84/fcell-10-1010232-g003.jpg

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本文引用的文献

[1]
DRP1 interacts directly with BAX to induce its activation and apoptosis.

EMBO J. 2022-4-19

[2]
Mitochondrial dynamics and its impact on human health and diseases: inside the DRP1 blackbox.

J Mol Med (Berl). 2022-1

[3]
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J Cell Biol. 2021-11-1

[4]
Mitochondrial adaptor TRAK2 activates and functionally links opposing kinesin and dynein motors.

Nat Commun. 2021-7-28

[5]
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Br J Haematol. 2021-6

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Hyperbaric oxygen alters intracellular bioenergetics distribution in human dermal fibroblasts.

Life Sci. 2021-8-1

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Front Endocrinol (Lausanne). 2021

[8]
Inhibition of mitochondrial carrier homolog 2 (MTCH2) suppresses tumor invasion and enhances sensitivity to temozolomide in malignant glioma.

Mol Med. 2021-1-28

[9]
Intricate role of mitochondrial calcium signalling in mitochondrial quality control for regulation of cancer cell fate.

Mitochondrion. 2021-3

[10]
Increased O-GlcNAcylation of Drp1 by amyloid-beta promotes mitochondrial fission and dysfunction in neuronal cells.

Mol Brain. 2021-1-9

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