Male SIRT1 insufficiency leads to sperm with decreased ability to hyperactivate and fertilize
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
the Ministry of Education, Youth and Sports
Charles University
PubMed
35668641
DOI
10.1111/rda.14172
Knihovny.cz E-zdroje
- Klíčová slova
- SIRT1, hyperactivated motility, infertility, sperm capacitation,
- MeSH
- adenosintrifosfát metabolismus MeSH
- fertilizace fyziologie MeSH
- kapacitace spermií MeSH
- motilita spermií MeSH
- mužská infertilita * genetika metabolismus veterinární MeSH
- myši MeSH
- sirtuin 1 genetika metabolismus MeSH
- sperma MeSH
- spermie fyziologie MeSH
- superoxidy MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- adenosintrifosfát MeSH
- Sirt1 protein, mouse MeSH Prohlížeč
- sirtuin 1 MeSH
- superoxidy MeSH
Deficient sperm motility is a frequent cause of the age-related male sub-/infertility. Since the protein sirtuin 1 (SIRT1) develops anti-aging action and participates in sperm motility and ATP synthesis in mitochondria, we investigated its role in the acquisition of hyperactivated motility during capacitation. For this, the dynamics of sperm subpopulations were studied, using males of Sirt1+/- heterozygous mutant mice. After 2 hr of capacitation, we observed reduced percentage of hyperactivated spermatozoa in Sirt1+/- males. Interestingly, prior to capacitation, Sirt1+/- spermatozoa showed higher mitochondrial superoxide levels, which could render mitochondrial injury and thereby motility defects. Accordingly, the fertilization rate of Sirt1+/- males after mating was decreased. We elucidated that SIRT1 male insufficiency underlies posterior sperm defects to hyperactivate during capacitation and propose Sirt1+/- males as a model for the study of the age-related infertility.
Biomedical Centre Faculty of Medicine in Pilsen Charles University Pilsen Czech Republic
Zobrazit více v PubMed
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