Maturation‐associated changes in the rat zona pellucida

Onit Rufas, Ruth Shalgi*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Rat follicular oocytes, arrested at prophase I, cannot be fertilized in vitro. This capacity is acquired following resumption of meiosis and a series of changes involving both the oocyte and the cumulus cells surrounding it. Oocytes exposed to sperm at different hours before ovulation show a gradual increase in the permeability of their zona pellucida (ZP). Our study examined whether the ZP, in response to the physiological stimulus for maturation and concomitant with the other oocyte—cumulus components, undergoes maturational changes. Two ZP characteristics were assessed, sensitivity to proteolysis and sperm binding. ZP surrounding oocytes and eggs were collected from five sources: 1) germinal vesicle (GV)‐intact oocytes, 2) preovulatory eggs, 3) ovulated eggs isolated from oviducts of immature females, 4) fertilized eggs, 5) ovulated eggs isolated from oviducts of mature females. All ZP surrounding oocytes/eggs from groups 1–5 were dissolved by trypsin. When solubility by pronase and α‐chymotrypsin was examined, a large variation between groups was found. All ZP from group 2 were dissolved by 0.001% pronase, compared to 0% solubility in group 4. Only 10% of the ZP surrounding GV‐intact oocytes (group 1) were dissolved by this enzyme, compared to 82% in group 3. Solubility in 0.01% α‐chymotrypsin showed a similar pattern. Capacitated sperm were incubated with eggs from groups 1 and 3. The number of sperm binding to ZP in group 3 was repeatedly higher than that in group 1. In both tests it was found that the ZP surrounding the mature eggs differ in their characteristics from ZP of GV‐intact oocytes. These variations may reflect a series of events in the ZP initiated by the GV breakdown and completed with the production of a mature fertilizable egg.

Original languageEnglish
Pages (from-to)324-330
Number of pages7
JournalMolecular Reproduction and Development
Volume26
Issue number4
DOIs
StatePublished - Aug 1990

Keywords

  • Pronase
  • Proteolysis
  • Sperm binding
  • α‐Chymotrypsin

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