4.6 Article

Sperm degradation after vasectomy follows a sperm chromatin fragmentation-dependent mechanism causing DNA breaks in the toroid linker regions

期刊

MOLECULAR HUMAN REPRODUCTION
卷 29, 期 9, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/molehr/gaac029

关键词

vasectomy; sperm degradation; sperm chromatin fragmentation; DNA damage; vas deferens; epididymis

资金

  1. European Union's Horizon 2020 Research and Innovation Scheme under the Marie Sklodowska-Curie grant [801342, TECSPR-191-0003]
  2. NIH [GM123048]
  3. Catalan Agency for Management of University and Research Grants, Regional Government of Catalonia, Spain [2017-SGR-1229]
  4. Catalan Institution for Research and Advanced Studies (ICREA)
  5. La Maratode TV3 Foundation [214/857-202039]

向作者/读者索取更多资源

Vasectomy can activate sperm chromatin fragmentation (SCF) as a mechanism to degrade sperm DNA that cannot be ejaculated, preventing their function. The study found that double-strand breaks were increased in vas deferens sperm after vasectomy, mainly occurring in the toroid linker regions (TLRs).
Vasectomy is a widely used surgical technique creating an obstructive azoospermia. Although sperm cannot be ejaculated, the testis maintains sperm production in vasectomized males. The continuous accumulation of sperm deposited in the epididymis and the vas deferens fraction necessarily need to be degraded and eliminated. While the elimination process is carried out by granulomas that form after vasectomy, the detailed mechanisms of sperm degradation are still not known. The aim was to assess whether sperm chromatin fragmentation (SCF), a mechanism that degrades the entire sperm genome at the toroid linker regions (TLRs), is activated after vasectomy in sperm cells. We vasectomized mice and evaluated the presence of TLR-specific double-strand breaks through pulsed-field gel electrophoresis and the Comet assay at 1, 2 and 3 weeks after surgery. Results for DNA damage (Olive tail moment) at single-cell level showed an increase of double-strand breaks after vasectomy for vas deferens sperm after 1, 2 and 3 weeks postvasectomy (21.78 +/- 2.29; 19.71 +/- 1.79 and 32.59 +/- 1.81, respectively), compared to mock surgery (7.04 +/- 1.03; 10.10 +/- 1.29 and 8.64 +/- 0.85, respectively; P < 0.001). Similar findings were obtained for cauda epididymis sperm (P < 0.001), but not for caput epididymis (P > 0.05). Pulsed-field gel electrophoresis showed the presence of double-stranded breaks between 15 and 145 kb, indicating that DNA breaks were produced mainly in the sperm TLRs. Results presented here suggest that SCF is a mechanism activated in vas deferens after vasectomy to degrade sperm DNA when they cannot be ejaculated, preventing their function.

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