Roles of the zona pellucida and functional exposure of the sperm-egg fusion factor 'IZUMO' during in vitro fertilization in pigs

Anim Sci J. 2014 Apr;85(4):395-404. doi: 10.1111/asj.12164. Epub 2014 Jan 23.

Abstract

The zona pellucida (ZP) is considered to play important roles in the prevention of polyspermy in mammalian oocytes. However, in pigs we have shown that the presence of the ZP accelerates sperm penetration into the ooplasm during in vitro fertilization (IVF). In the present study, we investigated the effects of the ZP on sperm binding, acrosomal status, and functional exposure of IZUMO, a critical factor involved in sperm-egg fusion, during IVF in pigs. We evaluated the numbers and acrosomal statuses of sperm binding to the ZP and oolemma, and being present in the ZP and perivitelline space (PVS) using ZP-intact and ZP-free oocytes. More sperm bound to the ZP than to the oolemma. The average number of sperm present in the PVS was 0.44-0.51 per oocyte, and all sperm had lost their acrosomes. The proportion of sperm that were immunopositive for anti-IZUMO antibody was significantly higher after they were passing or had passed through the ZP. Furthermore, addition of anti-IZUMO antibody to the fertilization medium significantly inhibited the penetration of sperm into ZP-free oocytes. These results suggest that, in pigs, the ZP induces the acrosome reaction, which is associated with the functional exposure of IZUMO, resulting in completion of fertilization.

Keywords: IZUMO; fertilization; oocyte; pig; zona pellucida.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrosome Reaction / drug effects
  • Animals
  • Female
  • Fertilization / drug effects*
  • Fertilization in Vitro*
  • Immunoglobulins / pharmacology*
  • In Vitro Techniques
  • Male
  • Membrane Proteins / pharmacology*
  • Oocytes / physiology*
  • Sperm-Ovum Interactions / drug effects*
  • Spermatozoa / physiology*
  • Swine
  • Zona Pellucida / physiology*

Substances

  • IZUMO1 protein, human
  • Immunoglobulins
  • Membrane Proteins