A comprehensive insight into the contribution of epigenetics in male infertility; focusing on immunological modifications

J Reprod Immunol. 2024 Aug:164:104274. doi: 10.1016/j.jri.2024.104274. Epub 2024 Jun 4.

Abstract

Numerous recent studies have examined the impact epigenetics-including DNA methylation-has on spermatogenesis and male infertility. Differential methylation of several genes has been linked to compromised spermatogenesis and/or reproductive failure. Specifically, male infertility has been frequently associated with DNA methylation abnormalities of MEST and H19 inside imprinted genes and MTHFR within non-imprinted genes. Microbial infections mainly result in male infertility because of the immune response triggered by the bacteria' accumulation of immune cells, proinflammatory cytokines, and chemokines. Thus, bacterially produced epigenetic dysregulations may impact host cell function, supporting host defense or enabling pathogen persistence. So, it is possible to think of pathogenic bacteria as potential epimutagens that can alter the epigenome. It has been demonstrated that dysregulated levels of LncRNA correlate with motility and sperm count in ejaculated spermatozoa from infertile males. Therefore, a thorough understanding of the relationship between decreased reproductive capacity and sperm DNA methylation status should aid in creating new diagnostic instruments for this condition. To fully understand the mechanisms influencing sperm methylation and how they relate to male infertility, more research is required.

Keywords: Bacterial infection; Epigenetic; Immune system; Male infertility; Modifications.

Publication types

  • Review

MeSH terms

  • Animals
  • Bacterial Infections / genetics
  • Bacterial Infections / immunology
  • DNA Methylation* / immunology
  • Epigenesis, Genetic* / immunology
  • Humans
  • Infertility, Male* / genetics
  • Infertility, Male* / immunology
  • Infertility, Male* / microbiology
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics
  • RNA, Long Noncoding / genetics
  • RNA, Long Noncoding / immunology
  • Spermatogenesis* / genetics
  • Spermatogenesis* / immunology
  • Spermatozoa* / immunology

Substances

  • RNA, Long Noncoding
  • H19 long non-coding RNA
  • Methylenetetrahydrofolate Reductase (NADPH2)