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Updated: Mar 18, 2026

Immunohistochemical Detection of 5-Methylcytosine and 5-Hydroxymethylcytosine in Developing and Postmitotic Mouse Retina
Published on: August 29, 2018
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.
Abstract:
Mammalian spermatogenesis is a progressive process comprising spermatogonial proliferation, spermatocytic meiosis, and later spermiogenesis, which is considered to be under the regulation of epigenetic parameters. To gain insights into the significance of DNA methylation in early spermatogenesis, 5-azadC was used as a molecular biological tool to mimic the level of DNA methylation in vivo. Since the drug is incorporated into DNA during the S-phase, spermatogonia and spermatocytes would be affected primarily in mouse spermatogenesis. Adult male ICR mice were intraperitoneally injected with 5-azadC at a dose of 0.25mg/kg/day for 10 consecutive days, allowing us to examine its maximum effect on the kinetics of spermatogonia and spermatocytes. In this short-term protocol, 5-azadC induced significant histological abnormalities, such as a marked increase in apoptosis of spermatogonia and spermatocytes, followed by severe loss of spermatids, while after termination of 5-azadC treatment, normal histology was restored in the testis within 35days. Quantification of the methylation level of CCGG sites as well as whole DNA showed spermatogonial hypomethylation, which correlated with increased apoptosis of spermatogonia. Interestingly, the hypomethylated cells were simultaneously positive for tri-methylated histone H3 at K4. On the other hand, no changes in methylation level were found in spermatocytes, but PCNA staining clearly showed disordered accumulation of S-phase spermatocytes, which increased their apoptosis in stage XII. In addition, different immunohistochemical staining pattern was found for DNA methyltransferases (DNMTs); DNMT1was expressed in the majority of all germ cells, but DNMT3a and b were only expressed in spermatogonia. Our results indicate that 5-azadC caused DNA hypomethylation in spermatogonia, but induced prolongation of S-phase in spermatocytes, resulting in the induction of apoptosis in both cases. Thus, 5-azadC affects spermatogenesis at more than one differentiation stage with different mechanisms, probably due to the specific usage of DNMTs.
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.
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