Cell-free mitochondrial DNA increases granulosa cell apoptosis and reduces aged oocyte blastocyst development in the mouse

Reprod Toxicol. 2020 Dec:98:278-285. doi: 10.1016/j.reprotox.2020.10.012. Epub 2020 Nov 2.

Abstract

Cell-free mitochondrial DNA (cf-mtDNA) released into the extracellular environment can cause cellular inflammatory responses and damage. Here, we investigated the effects of cf-mtDNA on mouse ovarian granulosa cell function and on the developmental competence of oocytes matured in vitro. Granulosa cells in the cf-mtDNA treatment group had a lower ATP content (P < 0.05), a higher apoptotic cell percentage (P < 0.01), and higher mRNA and protein levels of apoptosis-related factors than the control group (P < 0.01). TLR9, NF-кB p65 and MAPK p38 expression levels in granulosa cells were significantly increased in the cf-mtDNA treatment group (P < 0.05). The blastocyst formation rate of aged mice oocytes matured in vitro decreased significantly (P < 0.05) when cf-mtDNA was added to the media, compared with the control. However, the oocytes from young mice were not affected. Our results suggest that cf-mtDNA may impair granulosa cell function and induce granulosa cell apoptosis, subsequently decreasing blastocyst development in aged oocytes. This role of cf-mtDNA may be associated with the binding to TLR9 and the activation of NF-кB p65 and MAPK p38 signaling pathways.

Keywords: apoptosis; blastulation; cell free mitochondrial DNA; granulosa cells; oocyte.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Apoptosis
  • Apoptosis Regulatory Proteins / genetics
  • Apoptosis Regulatory Proteins / metabolism
  • Blastocyst / physiology*
  • Cell-Free Nucleic Acids*
  • DNA, Mitochondrial*
  • Embryonic Development
  • Female
  • Granulosa Cells / physiology*
  • Male
  • Membrane Potential, Mitochondrial
  • Mice, Inbred C57BL
  • Oocytes / physiology*
  • Oogenesis
  • Spermatozoa / physiology
  • Toll-Like Receptor 9 / metabolism
  • Transcription Factor RelA / metabolism
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Apoptosis Regulatory Proteins
  • Cell-Free Nucleic Acids
  • DNA, Mitochondrial
  • Tlr9 protein, mouse
  • Toll-Like Receptor 9
  • Transcription Factor RelA
  • Adenosine Triphosphate
  • p38 Mitogen-Activated Protein Kinases