A sea urchin egg jelly peptide induces a cGMP-mediated decrease in sperm intracellular Ca(2+) before its increase |
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Authors: | Nishigaki Takuya Wood Christopher D Tatsu Yoshiro Yumoto Noboru Furuta Toshiaki Elias David Shiba Kogiku Baba Shoji A Darszon Alberto |
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Institution: | a Department of Developmental Genetics and Molecular Physiology, Institute of Biotechnology, UNAM, Cuernavaca, Morelos 62210, Mexico b National Institute of Advanced Industrial Science and Technology (AIST), Midorigaoka, Ikeda 563-8577, Japan c PRESTO, JST and Department of Biomolecular Science, Toho University, Funabashi 274-8510, Japan d Bioelectronics Section, Department Electrical Engineering, Cinvestav-IPN, Mexico City, Mexico e Department of Biology, Ochanomizu University, Tokyo 112-8610, Japan |
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Abstract: | Speract, a sperm-activating peptide (SAP) from sea urchin eggs, increases the intracellular concentration of Ca2+ (Ca2+]i) and modulates sperm motility. We measured the initial sperm response to speract using its caged analog and observed, for the first time, a small but significant decrease in sperm Ca2+]i before the increase. Both directions of the Ca2+]i change were completely blocked in high K+ seawater. Using membrane-permeant caged cyclic nucleotides (cNMP), only cGMP induced the decrease in Ca2+]i although both cGMP and cAMP increased the Ca2+]i. The decrease in the Ca2+]i induced by cGMP was more notable following a second photolytic event, once Ca2+]i had been elevated by an initial flash. This pattern of Ca2+]i change was confirmed in individual sperm. These results together with pharmacological evidence suggest that the initial Ca2+]i decrease is due to a Na+/Ca2+ exchanger activity, stimulated by hyperpolarization mediated by K+ efflux through cGMP-regulated K+ channels. |
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Keywords: | Speract Sperm activation Caged peptide Caged cyclic nucleotides Time-resolved Ca2+ measurement Ca2+ imaging Sperm chemotaxis Na+/Ca2+ exchanger Membrane potential Ion channel |
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