Ca2+ Entry through Store-operated Channels in Mouse Sperm Is Initiated by Egg ZP3 and Drives the Acrosome Reaction

Author:

O'Toole Christine M.B.1,Arnoult Christophe2,Darszon Alberto3,Steinhardt Richard A.4,Florman Harvey M.1

Affiliation:

1. Department of Cell Biology, University of Massachusetts Medical School, Worcester, Massachusetts 01655;

2. Centre d'Etudes de Grenoble, Departement de Biologie Moleculaire et Structurale, 38054 Grenoble, France;

3. Department Genètica y Fisiologı̀a Molecular, Instituto d Biotecnologia, Cuernavaca, Morelos 62210, Mèxico; and

4. Department of Molecular and Cell Biology, University of California, Berkeley, California 94720

Abstract

Fertilization occurs after the completion of the sperm acrosome reaction, a secretory event that is triggered during gamete adhesion. ZP3, an egg zona pellucida glycoprotein, produces a sustained increase of the internal Ca2+ concentration in mouse sperm, leading to acrosome reactions. Here we show that the sustained Ca2+concentration increase is due to the persistent activation of a Ca2+ influx mechanism during the late stages of ZP3 signal transduction. These cells also possess a Ca2+ store depletion–activated Ca2+ entry pathway that is open after treatment with thapsigargin. Thapsigargin and ZP3 activate the same Ca2+ permeation mechanism, as demonstrated by fluorescence quenching experiments and by channel antagonists. These studies show that ZP3 generates a sustained Ca2+ influx through a store depletion–operated pathway and that this drives the exocytotic acrosome reaction.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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