2-APB-potentiated channels amplify CatSper-induced Ca2+ signals in human sperm

Author:

Lefièvre Linda12,Nash Katherine3,Mansell Steven4,Costello Sarah3,Punt Emma3,Correia Joao23,Morris Jennifer3,Kirkman-Brown Jackson12,Wilson Stuart M.4,Barratt Christopher L. R.4,Publicover Stephen3

Affiliation:

1. Medical School, University of Birmingham, Birmingham B15 2TT, U.K.

2. Birmingham Women's Hospital, Birmingham B15 2TG, U.K.

3. School of Biosciences, University of Birmingham, Birmingham B15 2TT, U.K.

4. Division of Cardiovascular Medicine, Medical Research Institute, Ninewells Hospital University of Dundee, Dundee DD1 9SY, Scotland, U.K.

Abstract

Ca2+i signalling is pivotal to sperm function. Progesterone, the best-characterized agonist of human sperm Ca2+i signalling, stimulates a biphasic [Ca2+]i rise, comprising a transient and subsequent sustained phase. In accordance with recent reports that progesterone directly activates CatSper, the [Ca2+]i transient was detectable in the anterior flagellum (where CatSper is expressed) 1–2 s before responses in the head and neck. Pre-treatment with 5 μM 2-APB (2-aminoethoxydiphenyl borate), which enhances activity of store-operated channel proteins (Orai) by facilitating interaction with their activator [STIM (stromal interaction molecule)] ‘amplified’ progesterone-induced [Ca2+]i transients at the sperm neck/midpiece without modifying kinetics. The flagellar [Ca2+]i response was unchanged. 2-APB (5 μM) also enhanced the sustained response in the midpiece, possibly reflecting mitochondrial Ca2+ accumulation downstream of the potentiated [Ca2+]i transient. Pre-treatment with 50–100 μM 2-APB failed to potentiate the transient and suppressed sustained [Ca2+]i elevation. When applied during the [Ca2+]i plateau, 50–100 μM 2-APB caused a transient fall in [Ca2+]i, which then recovered despite the continued presence of 2-APB. Loperamide (a chemically different store-operated channel agonist) enhanced the progesterone-induced [Ca2+]i signal and potentiated progesterone-induced hyperactivated motility. Neither 2-APB nor loperamide raised pHi (which would activate CatSper) and both compounds inhibited CatSper currents. STIM and Orai were detected and localized primarily to the neck/midpiece and acrosome where Ca2+ stores are present and the effects of 2-APB are focussed, but store-operated currents could not be detected in human sperm. We propose that 2-APB-sensitive channels amplify [Ca2+]i elevation induced by progesterone (and other CatSper agonists), amplifying, propagating and providing spatio-temporal complexity in [Ca2+]i signals of human sperm.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference59 articles.

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2. Rediscovering sperm ion channels with the patch-clamp technique;Kirichok;Mol. Hum. Reprod.,2011

3. The control of male fertility by spermatozoan ion channels;Lishko;Annu. Rev. Physiol.,2012

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5. Calcium signaling through CatSper channels in mammalian fertilization;Ren;Physiology (Bethesda),2010

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