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ATP increases head volume in capacitated human sperm via a purinergic channel.

Authors :
López-González I
Sánchez-Cárdenas C
De la Vega-Beltrán JL
Alvarado-Quevedo B
Ocelotl-Oviedo JP
González-Cota AL
Aldana A
Orta G
Darszon A
Source :
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2023 Sep 03; Vol. 671, pp. 318-326. Date of Electronic Publication: 2023 Jun 03.
Publication Year :
2023

Abstract

Scanning ion-conductance microscopy allowed us to document an external Ca <superscript>2+</superscript> dependent ATP driven volume increase (ATPVI) in capacitated human sperm heads. We examined the involvement of purinergic receptors (PRs) P2X2R and P2X4R in ATPVI using their co-agonists progesterone and Ivermectin (Iver), and Cu <superscript>2+</superscript> , which co-activates P2X2Rs and inhibits P2X4Rs. Iver enhanced ATPVI and Cu <superscript>2+</superscript> and 5BDBD inhibited it, indicating P2X4Rs contributed to this response. Moreover, Cu <superscript>2+</superscript> and 5BDBD inhibited the ATP-induced acrosome reaction (AR) which was enhanced by Iver. ATP increased the concentration of intracellular Ca <superscript>2+</superscript> ([Ca <superscript>2+</superscript> ] <subscript>i</subscript> ) in >45% of individual sperm, most of which underwent AR monitored using FM4-64. Our findings suggest that human sperm P2X4R activation by ATP increases [Ca <superscript>2+</superscript> ] <subscript>i</subscript> mainly due to Ca <superscript>2+</superscript> influx which leads to a sperm head volume increase, likely involving acrosomal swelling, and resulting in AR.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2023 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1090-2104
Volume :
671
Database :
MEDLINE
Journal :
Biochemical and biophysical research communications
Publication Type :
Academic Journal
Accession number :
37327703
Full Text :
https://doi.org/10.1016/j.bbrc.2023.06.008