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Mitofusins: from mitochondria to fertility

Authors
  • Zhao, Shanjiang
  • Heng, Nuo
  • Wang, Huan
  • Wang, Haoyu
  • Zhang, Haobo
  • Gong, Jianfei
  • Hu, Zhihui
  • Zhu, Huabin
Type
Published Article
Journal
Cellular and Molecular Life Sciences
Publisher
Springer-Verlag
Publication Date
Jun 20, 2022
Volume
79
Issue
7
Identifiers
DOI: 10.1007/s00018-022-04386-z
PMID: 35725948
PMCID: PMC9209398
Source
PubMed Central
Keywords
Disciplines
  • Review
License
Unknown

Abstract

Germ cell formation and embryonic development require ATP synthesized by mitochondria. The dynamic system of the mitochondria, and in particular, the fusion of mitochondria, are essential for the generation of energy. Mitofusin1 and mitofusin2, the homologues of Fuzzy onions in yeast and Drosophila, are critical regulators of mitochondrial fusion in mammalian cells. Since their discovery mitofusins (Mfns) have been the source of significant interest as key influencers of mitochondrial dynamics, including membrane fusion, mitochondrial distribution, and the interaction with other organelles. Emerging evidence has revealed significant insight into the role of Mfns in germ cell formation and embryonic development, as well as the high incidence of reproductive diseases such as asthenospermia, polycystic ovary syndrome, and gestational diabetes mellitus. Here, we describe the key mechanisms of Mfns in mitochondrial dynamics, focusing particularly on the role of Mfns in the regulation of mammalian fertility, including spermatogenesis, oocyte maturation, and embryonic development. We also highlight the role of Mfns in certain diseases associated with the reproductive system and their potential as therapeutic targets.

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