1. Academic Validation
  2. A delayed sperm penetration of cumulus layers by disruption of acrosin gene in rats

A delayed sperm penetration of cumulus layers by disruption of acrosin gene in rats

  • Biol Reprod. 2017 Jul 1;97(1):61-68. doi: 10.1093/biolre/iox066.
Ayako Isotani 1 2 3 Takafumi Matsumura 2 4 Masaki Ogawa 2 4 Takahiro Tanaka 2 5 Kazuo Yamagata 2 6 Masahito Ikawa 1 2 4 5 Masaru Okabe 2
Affiliations

Affiliations

  • 1 Immunology Frontier Research Center, Osaka University, Suita, Osaka, Japan.
  • 2 Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
  • 3 Graduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5 Takayama-cho, Ikoma, Nara, Japan.
  • 4 Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka, Japan.
  • 5 Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
  • 6 Department of Genetic Engineering, Faculty of Biology-Oriented Science and Technology, KINDAI University, 930 Nishimitani, Kinokawa, Wakayama, Japan.
Abstract

Acrosin, the trypsin-like serine protease in the sperm acrosome, was long viewed as a key Enzyme required for zona pellucida penetration to fertilize eggs. However, gene disruption experiments in mice surprisingly showed that acrosin-disrupted males were fertile. Thus, the acrosin was considered to be not an essential Enzyme for fertilization in mice. However, the involvement of acrosin in fertilization has been suggested in various species such as rat, bull, and pig. Moreover, it has been reported that serine protease (including acrosin) activity in mice is significantly weaker compared to Other species, including rats. We analyzed the role of acrosin by disrupting the rat acrosin gene. It was found that, unlike in mice, acrosin was almost the sole source of serine protease in rat spermatozoa. Nevertheless, the acrosin-disrupted males were not infertile. However, the litter size from acrosin-disrupted males was decreased compared to heterozygous mutant rats. Further investigation using an in vitro fertilization system revealed that the acrosin-disrupted spermatozoa possessed an equal ability to penetrate the zona pellucida with wild-type spermatozoa, but the cumulus cell dispersal was slower compared to wild-type and heterozygous spermatozoa. This delay was presumed to be the cause of the small litter size of acrosin-disrupted male rats.

Keywords

acrosin; fertilization; knock-out rat.

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