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Capacitation promotes a shift in energy metabolism in murine sperm
In mammals, sperm acquire fertilization ability after a series of physiological and biochemical changes, collectively known as capacitation, that occur inside the female reproductive tract. In addition to other requirements, sperm bioenergetic metabolism has been identified as a fundamental componen...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445201/ https://www.ncbi.nlm.nih.gov/pubmed/36081906 http://dx.doi.org/10.3389/fcell.2022.950979 |
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author | Tourmente, Maximiliano Sansegundo, Ester Rial, Eduardo Roldan, Eduardo R. S. |
author_facet | Tourmente, Maximiliano Sansegundo, Ester Rial, Eduardo Roldan, Eduardo R. S. |
author_sort | Tourmente, Maximiliano |
collection | PubMed |
description | In mammals, sperm acquire fertilization ability after a series of physiological and biochemical changes, collectively known as capacitation, that occur inside the female reproductive tract. In addition to other requirements, sperm bioenergetic metabolism has been identified as a fundamental component in the acquisition of capacitation. Mammalian sperm produce ATP through two main metabolic processes, oxidative phosphorylation (OXPHOS) and aerobic glycolysis that are localized to two different flagellar compartments, the midpiece, and the principal piece, respectively. In mouse sperm, the occurrence of many events associated with capacitation relies on the activity of these two energy-producing pathways, leading to the hypothesis that some of these events may impose changes in sperm energetic demands. In the present study, we used extracellular flux analysis to evaluate changes in glycolytic and respiratory parameters of murine sperm that occur as a consequence of capacitation. Furthermore, we examined whether these variations affect sperm ATP sustainability. Our results show that capacitation promotes a shift in the usage ratio of the two main metabolic pathways, from oxidative to glycolytic. However, this metabolic rewiring does not seem to affect the rate at which the sperm consume ATP. We conclude that the probable function of the metabolic switch is to increase the ATP supply in the distal flagellar regions, thus sustaining the energetic demands that arise from capacitation. |
format | Online Article Text |
id | pubmed-9445201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94452012022-09-07 Capacitation promotes a shift in energy metabolism in murine sperm Tourmente, Maximiliano Sansegundo, Ester Rial, Eduardo Roldan, Eduardo R. S. Front Cell Dev Biol Cell and Developmental Biology In mammals, sperm acquire fertilization ability after a series of physiological and biochemical changes, collectively known as capacitation, that occur inside the female reproductive tract. In addition to other requirements, sperm bioenergetic metabolism has been identified as a fundamental component in the acquisition of capacitation. Mammalian sperm produce ATP through two main metabolic processes, oxidative phosphorylation (OXPHOS) and aerobic glycolysis that are localized to two different flagellar compartments, the midpiece, and the principal piece, respectively. In mouse sperm, the occurrence of many events associated with capacitation relies on the activity of these two energy-producing pathways, leading to the hypothesis that some of these events may impose changes in sperm energetic demands. In the present study, we used extracellular flux analysis to evaluate changes in glycolytic and respiratory parameters of murine sperm that occur as a consequence of capacitation. Furthermore, we examined whether these variations affect sperm ATP sustainability. Our results show that capacitation promotes a shift in the usage ratio of the two main metabolic pathways, from oxidative to glycolytic. However, this metabolic rewiring does not seem to affect the rate at which the sperm consume ATP. We conclude that the probable function of the metabolic switch is to increase the ATP supply in the distal flagellar regions, thus sustaining the energetic demands that arise from capacitation. Frontiers Media S.A. 2022-08-23 /pmc/articles/PMC9445201/ /pubmed/36081906 http://dx.doi.org/10.3389/fcell.2022.950979 Text en Copyright © 2022 Tourmente, Sansegundo, Rial and Roldan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Tourmente, Maximiliano Sansegundo, Ester Rial, Eduardo Roldan, Eduardo R. S. Capacitation promotes a shift in energy metabolism in murine sperm |
title | Capacitation promotes a shift in energy metabolism in murine sperm |
title_full | Capacitation promotes a shift in energy metabolism in murine sperm |
title_fullStr | Capacitation promotes a shift in energy metabolism in murine sperm |
title_full_unstemmed | Capacitation promotes a shift in energy metabolism in murine sperm |
title_short | Capacitation promotes a shift in energy metabolism in murine sperm |
title_sort | capacitation promotes a shift in energy metabolism in murine sperm |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445201/ https://www.ncbi.nlm.nih.gov/pubmed/36081906 http://dx.doi.org/10.3389/fcell.2022.950979 |
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