C-type natriuretic peptide improves maternally aged oocytes quality by inhibiting excessive PINK1/Parkin-mediated mitophagy

Elife. 2023 Oct 20:12:RP88523. doi: 10.7554/eLife.88523.

Abstract

The overall oocyte quality declines with aging, and this effect is strongly associated with a higher reactive oxygen species (ROS) level and the resultant oxidative damage. C-type natriuretic peptide (CNP) is a well-characterized physiological meiotic inhibitor that has been successfully used to improve immature oocyte quality during in vitro maturation. However, the underlying roles of CNP in maternally aged oocytes have not been reported. Here, we found that the age-related reduction in the serum CNP concentration was highly correlated with decreased oocyte quality. Treatment with exogenous CNP promoted follicle growth and ovulation in aged mice and enhanced meiotic competency and fertilization ability. Interestingly, the cytoplasmic maturation of aged oocytes was thoroughly improved by CNP treatment, as assessed by spindle/chromosome morphology and redistribution of organelles (mitochondria, the endoplasmic reticulum, cortical granules, and the Golgi apparatus). CNP treatment also ameliorated DNA damage and apoptosis caused by ROS accumulation in aged oocytes. Importantly, oocyte RNA-seq revealed that the beneficial effect of CNP on aged oocytes was mediated by restoration of mitochondrial oxidative phosphorylation, eliminating excessive mitophagy. CNP reversed the defective phenotypes in aged oocytes by alleviating oxidative damage and suppressing excessive PINK1/Parkin-mediated mitophagy. Mechanistically, CNP functioned as a cAMP/PKA pathway modulator to decrease PINK1 stability and inhibit Parkin recruitment. In summary, our results demonstrated that CNP supplementation constitutes an alternative therapeutic approach for advanced maternal age-related oocyte deterioration and may improve the overall success rates of clinically assisted reproduction in older women.

Keywords: C-natriuretic peptide; developmental biology; embryonic development; mitophagy; mouse; oocyte; reactive oxygen species; reproductive aging.

MeSH terms

  • Animals
  • Cumulus Cells / metabolism
  • Female
  • In Vitro Oocyte Maturation Techniques* / methods
  • Meiosis
  • Mice
  • Mitophagy
  • Natriuretic Peptide, C-Type* / genetics
  • Natriuretic Peptide, C-Type* / metabolism
  • Natriuretic Peptide, C-Type* / pharmacology
  • Oocytes / metabolism
  • Protein Kinases / metabolism
  • Reactive Oxygen Species / metabolism

Substances

  • Natriuretic Peptide, C-Type
  • Protein Kinases
  • Reactive Oxygen Species
  • NPPC protein, human
  • parkin protein
  • PTEN-induced putative kinase

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.