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Ion Channel Function During Oocyte Maturation and Fertilization

The proper maturation of both male and female gametes is essential for supporting fertilization and the early embryonic divisions. In the ovary, immature fully-grown oocytes that are arrested in prophase I of meiosis I are not able to support fertilization. Acquiring fertilization competence require...

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Autores principales: Carvacho, Ingrid, Piesche, Matthias, Maier, Thorsten J., Machaca, Khaled
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028574/
https://www.ncbi.nlm.nih.gov/pubmed/29998105
http://dx.doi.org/10.3389/fcell.2018.00063
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author Carvacho, Ingrid
Piesche, Matthias
Maier, Thorsten J.
Machaca, Khaled
author_facet Carvacho, Ingrid
Piesche, Matthias
Maier, Thorsten J.
Machaca, Khaled
author_sort Carvacho, Ingrid
collection PubMed
description The proper maturation of both male and female gametes is essential for supporting fertilization and the early embryonic divisions. In the ovary, immature fully-grown oocytes that are arrested in prophase I of meiosis I are not able to support fertilization. Acquiring fertilization competence requires resumption of meiosis which encompasses the remodeling of multiple signaling pathways and the reorganization of cellular organelles. Collectively, this differentiation endows the egg with the ability to activate at fertilization and to promote the egg-to-embryo transition. Oocyte maturation is associated with changes in the electrical properties of the plasma membrane and alterations in the function and distribution of ion channels. Therefore, variations on the pattern of expression, distribution, and function of ion channels and transporters during oocyte maturation are fundamental to reproductive success. Ion channels and transporters are important in regulating membrane potential, but also in the case of calcium (Ca(2+)), they play a critical role in modulating intracellular signaling pathways. In the context of fertilization, Ca(2+) has been shown to be the universal activator of development at fertilization, playing a central role in early events associated with egg activation and the egg-to-embryo transition. These early events include the block of polyspermy, the completion of meiosis and the transition to the embryonic mitotic divisions. In this review, we discuss the role of ion channels during oocyte maturation, fertilization and early embryonic development. We will describe how ion channel studies in Xenopus oocytes, an extensively studied model of oocyte maturation, translate into a greater understanding of the role of ion channels in mammalian oocyte physiology.
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spelling pubmed-60285742018-07-11 Ion Channel Function During Oocyte Maturation and Fertilization Carvacho, Ingrid Piesche, Matthias Maier, Thorsten J. Machaca, Khaled Front Cell Dev Biol Cell and Developmental Biology The proper maturation of both male and female gametes is essential for supporting fertilization and the early embryonic divisions. In the ovary, immature fully-grown oocytes that are arrested in prophase I of meiosis I are not able to support fertilization. Acquiring fertilization competence requires resumption of meiosis which encompasses the remodeling of multiple signaling pathways and the reorganization of cellular organelles. Collectively, this differentiation endows the egg with the ability to activate at fertilization and to promote the egg-to-embryo transition. Oocyte maturation is associated with changes in the electrical properties of the plasma membrane and alterations in the function and distribution of ion channels. Therefore, variations on the pattern of expression, distribution, and function of ion channels and transporters during oocyte maturation are fundamental to reproductive success. Ion channels and transporters are important in regulating membrane potential, but also in the case of calcium (Ca(2+)), they play a critical role in modulating intracellular signaling pathways. In the context of fertilization, Ca(2+) has been shown to be the universal activator of development at fertilization, playing a central role in early events associated with egg activation and the egg-to-embryo transition. These early events include the block of polyspermy, the completion of meiosis and the transition to the embryonic mitotic divisions. In this review, we discuss the role of ion channels during oocyte maturation, fertilization and early embryonic development. We will describe how ion channel studies in Xenopus oocytes, an extensively studied model of oocyte maturation, translate into a greater understanding of the role of ion channels in mammalian oocyte physiology. Frontiers Media S.A. 2018-06-26 /pmc/articles/PMC6028574/ /pubmed/29998105 http://dx.doi.org/10.3389/fcell.2018.00063 Text en Copyright © 2018 Carvacho, Piesche, Maier and Machaca. http://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 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
Carvacho, Ingrid
Piesche, Matthias
Maier, Thorsten J.
Machaca, Khaled
Ion Channel Function During Oocyte Maturation and Fertilization
title Ion Channel Function During Oocyte Maturation and Fertilization
title_full Ion Channel Function During Oocyte Maturation and Fertilization
title_fullStr Ion Channel Function During Oocyte Maturation and Fertilization
title_full_unstemmed Ion Channel Function During Oocyte Maturation and Fertilization
title_short Ion Channel Function During Oocyte Maturation and Fertilization
title_sort ion channel function during oocyte maturation and fertilization
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028574/
https://www.ncbi.nlm.nih.gov/pubmed/29998105
http://dx.doi.org/10.3389/fcell.2018.00063
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