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Slo1 is the principal potassium channel of human spermatozoa
Mammalian spermatozoa gain competence to fertilize an oocyte as they travel through the female reproductive tract. This process is accompanied by an elevation of sperm intracellular calcium and a membrane hyperpolarization. The latter is evoked by K(+) efflux; however, the molecular identity of the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789364/ https://www.ncbi.nlm.nih.gov/pubmed/24137539 http://dx.doi.org/10.7554/eLife.01009 |
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author | Mannowetz, Nadja Naidoo, Natasha M Choo, Seung-A Sara Smith, James F Lishko, Polina V |
author_facet | Mannowetz, Nadja Naidoo, Natasha M Choo, Seung-A Sara Smith, James F Lishko, Polina V |
author_sort | Mannowetz, Nadja |
collection | PubMed |
description | Mammalian spermatozoa gain competence to fertilize an oocyte as they travel through the female reproductive tract. This process is accompanied by an elevation of sperm intracellular calcium and a membrane hyperpolarization. The latter is evoked by K(+) efflux; however, the molecular identity of the potassium channel of human spermatozoa (hKSper) is unknown. Here, we characterize hKSper, reporting that it is regulated by intracellular calcium but is insensitive to intracellular alkalinization. We also show that human KSper is inhibited by charybdotoxin, iberiotoxin, and paxilline, while mouse KSper is insensitive to these compounds. Such unique properties suggest that the Slo1 ion channel is the molecular determinant for hKSper. We show that Slo1 is localized to the sperm flagellum and is inhibited by progesterone. Inhibition of hKSper by progesterone may depolarize the spermatozoon to open the calcium channel CatSper, thus raising [Ca(2+)] to produce hyperactivation and allowing sperm to fertilize an oocyte. DOI: http://dx.doi.org/10.7554/eLife.01009.001 |
format | Online Article Text |
id | pubmed-3789364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37893642013-10-17 Slo1 is the principal potassium channel of human spermatozoa Mannowetz, Nadja Naidoo, Natasha M Choo, Seung-A Sara Smith, James F Lishko, Polina V eLife Biophysics and Structural Biology Mammalian spermatozoa gain competence to fertilize an oocyte as they travel through the female reproductive tract. This process is accompanied by an elevation of sperm intracellular calcium and a membrane hyperpolarization. The latter is evoked by K(+) efflux; however, the molecular identity of the potassium channel of human spermatozoa (hKSper) is unknown. Here, we characterize hKSper, reporting that it is regulated by intracellular calcium but is insensitive to intracellular alkalinization. We also show that human KSper is inhibited by charybdotoxin, iberiotoxin, and paxilline, while mouse KSper is insensitive to these compounds. Such unique properties suggest that the Slo1 ion channel is the molecular determinant for hKSper. We show that Slo1 is localized to the sperm flagellum and is inhibited by progesterone. Inhibition of hKSper by progesterone may depolarize the spermatozoon to open the calcium channel CatSper, thus raising [Ca(2+)] to produce hyperactivation and allowing sperm to fertilize an oocyte. DOI: http://dx.doi.org/10.7554/eLife.01009.001 eLife Sciences Publications, Ltd 2013-10-08 /pmc/articles/PMC3789364/ /pubmed/24137539 http://dx.doi.org/10.7554/eLife.01009 Text en Copyright © 2013, Mannowetz et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Mannowetz, Nadja Naidoo, Natasha M Choo, Seung-A Sara Smith, James F Lishko, Polina V Slo1 is the principal potassium channel of human spermatozoa |
title | Slo1 is the principal potassium channel of human spermatozoa |
title_full | Slo1 is the principal potassium channel of human spermatozoa |
title_fullStr | Slo1 is the principal potassium channel of human spermatozoa |
title_full_unstemmed | Slo1 is the principal potassium channel of human spermatozoa |
title_short | Slo1 is the principal potassium channel of human spermatozoa |
title_sort | slo1 is the principal potassium channel of human spermatozoa |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789364/ https://www.ncbi.nlm.nih.gov/pubmed/24137539 http://dx.doi.org/10.7554/eLife.01009 |
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