Mitophagy and spermatogenesis: Role and mechanisms.

Autophagy Male infertility Reproductive health Spermatogenesis

Journal

Biochemistry and biophysics reports
ISSN: 2405-5808
Titre abrégé: Biochem Biophys Rep
Pays: Netherlands
ID NLM: 101660999

Informations de publication

Date de publication:
Jul 2024
Historique:
received: 08 03 2024
revised: 25 03 2024
accepted: 26 03 2024
medline: 5 4 2024
pubmed: 5 4 2024
entrez: 5 4 2024
Statut: epublish

Résumé

The mitophagy process, a type of macroautophagy, is the targeted removal of mitochondria. It is a type of autophagy exclusive to mitochondria, as the process removes defective mitochondria one by one. Mitophagy serves as an additional level of quality control by using autophagy to remove superfluous mitochondria or mitochondria that are irreparably damaged. During spermatogenesis, mitophagy can influence cell homeostasis and participates in a variety of membrane trafficking activities. Crucially, it has been demonstrated that defective mitophagy can impede spermatogenesis. Despite an increasing amount of evidence suggesting that mitophagy and mitochondrial dynamics preserve the fundamental level of cellular homeostasis, little is known about their role in developmentally controlled metabolic transitions and differentiation. It has been observed that male infertility is a result of mitophagy's impact on sperm motility. Furthermore, certain proteins related to autophagy have been shown to be present in mammalian spermatozoa. The mitochondria are the only organelle in sperm that can produce reactive oxygen species and finally provide energy for sperm movement. Furthermore, studies have shown that inhibited autophagy-infected spermatozoa had reduced motility and increased amounts of phosphorylated PINK1, TOM20, caspase 3/7, and AMPK. Therefore, in terms of reproductive physiology, mitophagy is the removal of mitochondria derived from sperm and the following preservation of mitochondria that are exclusively maternal.

Identifiants

pubmed: 38577271
doi: 10.1016/j.bbrep.2024.101698
pii: S2405-5808(24)00062-1
pmc: PMC10990862
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

101698

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

None.The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. The authors declare that they no known financial interests that could have appeared to influence the work reported in this paper.

Auteurs

Damilare Emmanuel Rotimi (DE)

Department of Biochemistry, Landmark University, Omu-Aran 251101, Kwara State, Nigeria.
SDG 3, Good Health & Well-being, Landmark University, Nigeria.

Matthew Iyobhebhe (M)

Department of Biochemistry, Landmark University, Omu-Aran 251101, Kwara State, Nigeria.
SDG 3, Good Health & Well-being, Landmark University, Nigeria.

Elizabeth Temidayo Oluwayemi (ET)

Department of Biochemistry, Landmark University, Omu-Aran 251101, Kwara State, Nigeria.
SDG 3, Good Health & Well-being, Landmark University, Nigeria.

Ikponmwosa Owen Evbuomwan (IO)

Department of Microbiology, Landmark University, PMB 1001, Omu-Aran-251101, Nigeria.

Rotdelmwa Maimako Asaleye (RM)

Department of Biochemistry, Landmark University, Omu-Aran 251101, Kwara State, Nigeria.
SDG 3, Good Health & Well-being, Landmark University, Nigeria.

Oluwafemi Adeleke Ojo (OA)

Department of Biochemistry, Bowen University, Iwo, Osun State, Nigeria.

Oluyomi Stephen Adeyemi (OS)

Department of Biochemistry, Bowen University, Iwo, Osun State, Nigeria.

Classifications MeSH