Cargando…

Ca(2+) Signals Generated by CatSper and Ca(2+) Stores Regulate Different Behaviors in Human Sperm

[Ca(2+)](i) signaling regulates sperm motility, enabling switching between functionally different behaviors that the sperm must employ as it ascends the female tract and fertilizes the oocyte. We report that different behaviors in human sperm are recruited according to the Ca(2+) signaling pathway u...

Descripción completa

Detalles Bibliográficos
Autores principales: Alasmari, Wardah, Costello, Sarah, Correia, Joao, Oxenham, Senga K., Morris, Jennifer, Fernandes, Leonor, Ramalho-Santos, Joao, Kirkman-Brown, Jackson, Michelangeli, Francesco, Publicover, Stephen, Barratt, Christopher L. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585060/
https://www.ncbi.nlm.nih.gov/pubmed/23344959
http://dx.doi.org/10.1074/jbc.M112.439356
_version_ 1782261098473324544
author Alasmari, Wardah
Costello, Sarah
Correia, Joao
Oxenham, Senga K.
Morris, Jennifer
Fernandes, Leonor
Ramalho-Santos, Joao
Kirkman-Brown, Jackson
Michelangeli, Francesco
Publicover, Stephen
Barratt, Christopher L. R.
author_facet Alasmari, Wardah
Costello, Sarah
Correia, Joao
Oxenham, Senga K.
Morris, Jennifer
Fernandes, Leonor
Ramalho-Santos, Joao
Kirkman-Brown, Jackson
Michelangeli, Francesco
Publicover, Stephen
Barratt, Christopher L. R.
author_sort Alasmari, Wardah
collection PubMed
description [Ca(2+)](i) signaling regulates sperm motility, enabling switching between functionally different behaviors that the sperm must employ as it ascends the female tract and fertilizes the oocyte. We report that different behaviors in human sperm are recruited according to the Ca(2+) signaling pathway used. Activation of CatSper (by raising pH(i) or stimulating with progesterone) caused sustained [Ca(2+)](i) elevation but did not induce hyperactivation, the whiplash-like behavior required for progression along the oviduct and penetration of the zona pellucida. In contrast, penetration into methylcellulose (mimicking penetration into cervical mucus or cumulus matrix) was enhanced by activation of CatSper. NNC55-0396, which abolishes CatSper currents in human sperm, inhibited this effect. Treatment with 5 μm thimerosal to mobilize stored Ca(2+) caused sustained [Ca(2+)](i) elevation and induced strong, sustained hyperactivation that was completely insensitive to NNC55-0396. Thimerosal had no effect on penetration into methylcellulose. 4-Aminopyridine, a powerful modulator of sperm motility, both raised pH(i) and mobilized Ca(2+) stored in sperm (and from microsomal membrane preparations). 4-Aminopyridine-induced hyperactivation even in cells suspended in Ca(2+)-depleted medium and also potentiated penetration into methylcellulose. The latter effect was sensitive to NNC55-039, but induction of hyperactivation was not. We conclude that these two components of the [Ca(2+)](i) signaling apparatus have strikingly different effects on sperm motility. Furthermore, since stored Ca(2+) at the sperm neck can be mobilized by Ca(2+)-induced Ca(2+) release, we propose that CatSper activation can elicit functionally different behaviors according to the sensitivity of the Ca(2+) store, which may be regulated by capacitation and NO from the cumulus.
format Online
Article
Text
id pubmed-3585060
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher American Society for Biochemistry and Molecular Biology
record_format MEDLINE/PubMed
spelling pubmed-35850602013-03-04 Ca(2+) Signals Generated by CatSper and Ca(2+) Stores Regulate Different Behaviors in Human Sperm Alasmari, Wardah Costello, Sarah Correia, Joao Oxenham, Senga K. Morris, Jennifer Fernandes, Leonor Ramalho-Santos, Joao Kirkman-Brown, Jackson Michelangeli, Francesco Publicover, Stephen Barratt, Christopher L. R. J Biol Chem Signal Transduction [Ca(2+)](i) signaling regulates sperm motility, enabling switching between functionally different behaviors that the sperm must employ as it ascends the female tract and fertilizes the oocyte. We report that different behaviors in human sperm are recruited according to the Ca(2+) signaling pathway used. Activation of CatSper (by raising pH(i) or stimulating with progesterone) caused sustained [Ca(2+)](i) elevation but did not induce hyperactivation, the whiplash-like behavior required for progression along the oviduct and penetration of the zona pellucida. In contrast, penetration into methylcellulose (mimicking penetration into cervical mucus or cumulus matrix) was enhanced by activation of CatSper. NNC55-0396, which abolishes CatSper currents in human sperm, inhibited this effect. Treatment with 5 μm thimerosal to mobilize stored Ca(2+) caused sustained [Ca(2+)](i) elevation and induced strong, sustained hyperactivation that was completely insensitive to NNC55-0396. Thimerosal had no effect on penetration into methylcellulose. 4-Aminopyridine, a powerful modulator of sperm motility, both raised pH(i) and mobilized Ca(2+) stored in sperm (and from microsomal membrane preparations). 4-Aminopyridine-induced hyperactivation even in cells suspended in Ca(2+)-depleted medium and also potentiated penetration into methylcellulose. The latter effect was sensitive to NNC55-039, but induction of hyperactivation was not. We conclude that these two components of the [Ca(2+)](i) signaling apparatus have strikingly different effects on sperm motility. Furthermore, since stored Ca(2+) at the sperm neck can be mobilized by Ca(2+)-induced Ca(2+) release, we propose that CatSper activation can elicit functionally different behaviors according to the sensitivity of the Ca(2+) store, which may be regulated by capacitation and NO from the cumulus. American Society for Biochemistry and Molecular Biology 2013-03-01 2013-01-23 /pmc/articles/PMC3585060/ /pubmed/23344959 http://dx.doi.org/10.1074/jbc.M112.439356 Text en © 2013 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access. Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) applies to Author Choice Articles
spellingShingle Signal Transduction
Alasmari, Wardah
Costello, Sarah
Correia, Joao
Oxenham, Senga K.
Morris, Jennifer
Fernandes, Leonor
Ramalho-Santos, Joao
Kirkman-Brown, Jackson
Michelangeli, Francesco
Publicover, Stephen
Barratt, Christopher L. R.
Ca(2+) Signals Generated by CatSper and Ca(2+) Stores Regulate Different Behaviors in Human Sperm
title Ca(2+) Signals Generated by CatSper and Ca(2+) Stores Regulate Different Behaviors in Human Sperm
title_full Ca(2+) Signals Generated by CatSper and Ca(2+) Stores Regulate Different Behaviors in Human Sperm
title_fullStr Ca(2+) Signals Generated by CatSper and Ca(2+) Stores Regulate Different Behaviors in Human Sperm
title_full_unstemmed Ca(2+) Signals Generated by CatSper and Ca(2+) Stores Regulate Different Behaviors in Human Sperm
title_short Ca(2+) Signals Generated by CatSper and Ca(2+) Stores Regulate Different Behaviors in Human Sperm
title_sort ca(2+) signals generated by catsper and ca(2+) stores regulate different behaviors in human sperm
topic Signal Transduction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585060/
https://www.ncbi.nlm.nih.gov/pubmed/23344959
http://dx.doi.org/10.1074/jbc.M112.439356
work_keys_str_mv AT alasmariwardah ca2signalsgeneratedbycatsperandca2storesregulatedifferentbehaviorsinhumansperm
AT costellosarah ca2signalsgeneratedbycatsperandca2storesregulatedifferentbehaviorsinhumansperm
AT correiajoao ca2signalsgeneratedbycatsperandca2storesregulatedifferentbehaviorsinhumansperm
AT oxenhamsengak ca2signalsgeneratedbycatsperandca2storesregulatedifferentbehaviorsinhumansperm
AT morrisjennifer ca2signalsgeneratedbycatsperandca2storesregulatedifferentbehaviorsinhumansperm
AT fernandesleonor ca2signalsgeneratedbycatsperandca2storesregulatedifferentbehaviorsinhumansperm
AT ramalhosantosjoao ca2signalsgeneratedbycatsperandca2storesregulatedifferentbehaviorsinhumansperm
AT kirkmanbrownjackson ca2signalsgeneratedbycatsperandca2storesregulatedifferentbehaviorsinhumansperm
AT michelangelifrancesco ca2signalsgeneratedbycatsperandca2storesregulatedifferentbehaviorsinhumansperm
AT publicoverstephen ca2signalsgeneratedbycatsperandca2storesregulatedifferentbehaviorsinhumansperm
AT barrattchristopherlr ca2signalsgeneratedbycatsperandca2storesregulatedifferentbehaviorsinhumansperm