5-aza-2'-deoxycytidine impairs mouse spermatogenesis at multiple stages through different usage of DNA

Ning Song1, Daisuke Endo2, Bin Song3

  • 1Department of Histology and Cell Biology, Nagasaki University Graduate School of Biomedical Sciences, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan; Department of Anatomy, Histology and Embryology, Shanghai Jiaotong University School of Medicine, 280 South Chongqing Rd., Shanghai 200025, PR China.

Toxicology
|July 12, 2016
PubMed

Insights

DNA methylation impacts mammalian spermatogenesis. 5-azadC treatment caused DNA hypomethylation in spermatogonia and S-phase prolongation in spermatocytes, leading to apoptosis and germ cell loss.

Area of Science:

  • Reproductive Biology
  • Epigenetics
  • Developmental Biology

Background:

  • Mammalian spermatogenesis involves complex epigenetic regulation.
  • DNA methylation is a key epigenetic parameter influencing germ cell development.
  • Understanding DNA methylation's role in early spermatogenesis is crucial.

Purpose of the Study:

  • To investigate the effects of DNA hypomethylation on early spermatogenesis using 5-azadC.
  • To analyze the impact of 5-azadC on spermatogonial and spermatocyte kinetics and apoptosis.
  • To explore the correlation between DNA methylation changes and histone modifications.

Main Methods:

  • Adult male ICR mice were treated with 5-azadC (0.25mg/kg/day for 10 days).
  • Histological analysis, apoptosis assessment, and DNA methylation quantification (CCGG sites and whole DNA) were performed.
  • Immunohistochemistry was used to detect DNA methyltransferases (DNMTs) and PCNA.

Main Results:

  • 5-azadC induced spermatogonial hypomethylation, increased apoptosis, and loss of spermatids.
  • Spermatocytes showed prolonged S-phase and increased apoptosis without changes in DNA methylation levels.
  • Hypomethylated spermatogonia exhibited trimethylated histone H3 at K4; DNMT1, DNMT3a, and DNMT3b expression patterns varied.

Conclusions:

  • 5-azadC disrupts spermatogenesis by inducing DNA hypomethylation in spermatogonia and S-phase prolongation in spermatocytes.
  • These disruptions lead to apoptosis and germ cell loss at distinct differentiation stages.
  • The findings highlight the differential mechanisms by which DNA methylation affects various stages of spermatogenesis.