Seasonal spermatogenesis, epididymal storage, and creatine kinase expression in Pelodiscus sinensis

Anim Reprod Sci. 2023 Feb:249:107198. doi: 10.1016/j.anireprosci.2023.107198. Epub 2023 Feb 10.

Abstract

The soft-shelled turtle, Pelodiscus sinensis, is an important economic aquaculture species. Its reproduction exhibits seasonality; however, there is a lack of systematic studies focused on sperm maturation and epididymal storage. The testes and epididymides of P. sinensis were sampled from March to December. The seasonal reproduction and maturation of the spermatozoa were examined by anatomy, hematoxylin and eosin staining, AB-PAS staining, and immunohistochemistry. Spermatogenesis exhibited obvious seasonality in P. sinensis. It was found that the spermatogenic epithelium was most active during June to September, whereas the diameter of the epididymal tubules was smallest during June to October. As key enzymes of ATP metabolism, creatine kinases were highly expressed in the epididymal tubule epithelium during the breeding season, which may be important for the regulation of sperm maturation. In addition, the epididymal tubule epithelium changed with the season in June to September, the epididymal tubule epithelium proliferated to form villous structures, and secreted a large number of glycoproteins, which may be related to the rapid maturation of sperm during the breeding season. In conclusion, this study provided insights into the spermatogenesis of P. sinensis through histological analysis and enriched our understanding of reproduction in reptiles.

Keywords: Pelodiscus sinensis; Seasonal reproduction; Sperm maturation; Spermatogenesis.

MeSH terms

  • Animals
  • Creatine Kinase* / genetics
  • Creatine Kinase* / metabolism
  • Epididymis* / cytology
  • Epididymis* / growth & development
  • Epididymis* / metabolism
  • Epithelium / anatomy & histology
  • Epithelium / growth & development
  • Gene Expression / physiology
  • Male
  • Seasons
  • Spermatogenesis*
  • Turtles*

Substances

  • Creatine Kinase