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Pharmacological Evidence Suggests That Slo3 Channel Is the Principal K(+) Channel in Boar Spermatozoa

Sperm ion channels are associated with the quality and type of flagellar movement, and their differential regulation is crucial for sperm function during specific phases. The principal potassium ion channel is responsible for the majority of K(+) ion flux, resulting in membrane hyperpolarization, an...

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Autores principales: Cooray, Akila, Kim, Jeongsook, Nirujan, Beno Ramesh, Jayathilake, Nishani Jayanika, Lee, Kyu Pil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10178124/
https://www.ncbi.nlm.nih.gov/pubmed/37175513
http://dx.doi.org/10.3390/ijms24097806
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author Cooray, Akila
Kim, Jeongsook
Nirujan, Beno Ramesh
Jayathilake, Nishani Jayanika
Lee, Kyu Pil
author_facet Cooray, Akila
Kim, Jeongsook
Nirujan, Beno Ramesh
Jayathilake, Nishani Jayanika
Lee, Kyu Pil
author_sort Cooray, Akila
collection PubMed
description Sperm ion channels are associated with the quality and type of flagellar movement, and their differential regulation is crucial for sperm function during specific phases. The principal potassium ion channel is responsible for the majority of K(+) ion flux, resulting in membrane hyperpolarization, and is essential for sperm capacitation-related signaling pathways. The molecular identity of the principal K(+) channel varies greatly between different species, and there is a lack of information about boar K(+) channels. We aimed to determine the channel identity of boar sperm contributing to the primary K(+) current using pharmacological dissection. A series of Slo1 and Slo3 channel modulators were used for treatment. Sperm motility and related kinematic parameters were monitored using a computer-assisted sperm analysis system under non-capacitated conditions. Time-lapse flow cytometry with fluorochromes was used to measure changes in different intracellular ionic concentrations, and conventional flow cytometry was used to determine the acrosome reaction. Membrane depolarization, reduction in acrosome reaction, and motility parameters were observed upon the inhibition of the Slo3 channel, suggesting that the Slo3 gene encodes the main K(+) channel in boar spermatozoa. The Slo3 channel was localized on the sperm flagellum, and the inhibition of Slo3 did not reduce sperm viability. These results may aid potential animal-model-based extrapolations and help to ameliorate motility and related parameters, leading to improved assisted reproductive methods in industrial livestock production.
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spelling pubmed-101781242023-05-13 Pharmacological Evidence Suggests That Slo3 Channel Is the Principal K(+) Channel in Boar Spermatozoa Cooray, Akila Kim, Jeongsook Nirujan, Beno Ramesh Jayathilake, Nishani Jayanika Lee, Kyu Pil Int J Mol Sci Article Sperm ion channels are associated with the quality and type of flagellar movement, and their differential regulation is crucial for sperm function during specific phases. The principal potassium ion channel is responsible for the majority of K(+) ion flux, resulting in membrane hyperpolarization, and is essential for sperm capacitation-related signaling pathways. The molecular identity of the principal K(+) channel varies greatly between different species, and there is a lack of information about boar K(+) channels. We aimed to determine the channel identity of boar sperm contributing to the primary K(+) current using pharmacological dissection. A series of Slo1 and Slo3 channel modulators were used for treatment. Sperm motility and related kinematic parameters were monitored using a computer-assisted sperm analysis system under non-capacitated conditions. Time-lapse flow cytometry with fluorochromes was used to measure changes in different intracellular ionic concentrations, and conventional flow cytometry was used to determine the acrosome reaction. Membrane depolarization, reduction in acrosome reaction, and motility parameters were observed upon the inhibition of the Slo3 channel, suggesting that the Slo3 gene encodes the main K(+) channel in boar spermatozoa. The Slo3 channel was localized on the sperm flagellum, and the inhibition of Slo3 did not reduce sperm viability. These results may aid potential animal-model-based extrapolations and help to ameliorate motility and related parameters, leading to improved assisted reproductive methods in industrial livestock production. MDPI 2023-04-25 /pmc/articles/PMC10178124/ /pubmed/37175513 http://dx.doi.org/10.3390/ijms24097806 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cooray, Akila
Kim, Jeongsook
Nirujan, Beno Ramesh
Jayathilake, Nishani Jayanika
Lee, Kyu Pil
Pharmacological Evidence Suggests That Slo3 Channel Is the Principal K(+) Channel in Boar Spermatozoa
title Pharmacological Evidence Suggests That Slo3 Channel Is the Principal K(+) Channel in Boar Spermatozoa
title_full Pharmacological Evidence Suggests That Slo3 Channel Is the Principal K(+) Channel in Boar Spermatozoa
title_fullStr Pharmacological Evidence Suggests That Slo3 Channel Is the Principal K(+) Channel in Boar Spermatozoa
title_full_unstemmed Pharmacological Evidence Suggests That Slo3 Channel Is the Principal K(+) Channel in Boar Spermatozoa
title_short Pharmacological Evidence Suggests That Slo3 Channel Is the Principal K(+) Channel in Boar Spermatozoa
title_sort pharmacological evidence suggests that slo3 channel is the principal k(+) channel in boar spermatozoa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10178124/
https://www.ncbi.nlm.nih.gov/pubmed/37175513
http://dx.doi.org/10.3390/ijms24097806
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