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Role of Type 1 Inositol 1,4,5-triphosphate Receptors in Mammalian Oocytes

The ability of oocytes to undergo normal fertilization and embryo development is acquired during oocyte maturation which is transition from the germinal vesicle stage (GV), germinal vesicle breakdown (GVBD) to metaphase of meiosis II (MII). Part of this process includes redistribution of inositol 1,...

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Autor principal: Yoon, Sook Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Developmental Biology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6487317/
https://www.ncbi.nlm.nih.gov/pubmed/31049467
http://dx.doi.org/10.12717/DR.2019.23.1.001
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author Yoon, Sook Young
author_facet Yoon, Sook Young
author_sort Yoon, Sook Young
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description The ability of oocytes to undergo normal fertilization and embryo development is acquired during oocyte maturation which is transition from the germinal vesicle stage (GV), germinal vesicle breakdown (GVBD) to metaphase of meiosis II (MII). Part of this process includes redistribution of inositol 1,4, 5-triphosphate receptor (IP3R), a predominant Ca(2+) channel on the endoplasmic reticulum membrane. Type 1 IP3R (IP3R1) is expressed in mouse oocytes dominantly. At GV stage, IP3R1 are arranged as a network throughout the cytoplasm with minute accumulation around the nucleus. At MII stage, IP3R1 diffuses to the entire cytoplasm in a more reticular manner, and obvious clusters of IP3R1 are observed at the cortex of the egg. This structural reorganization provides acquisition of [Ca(2+)](i) oscillatory activity during fertilization. In this review, general properties of IP3R1 in somatic cells and mammalian oocyte are introduced.
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spelling pubmed-64873172019-05-02 Role of Type 1 Inositol 1,4,5-triphosphate Receptors in Mammalian Oocytes Yoon, Sook Young Dev Reprod Review The ability of oocytes to undergo normal fertilization and embryo development is acquired during oocyte maturation which is transition from the germinal vesicle stage (GV), germinal vesicle breakdown (GVBD) to metaphase of meiosis II (MII). Part of this process includes redistribution of inositol 1,4, 5-triphosphate receptor (IP3R), a predominant Ca(2+) channel on the endoplasmic reticulum membrane. Type 1 IP3R (IP3R1) is expressed in mouse oocytes dominantly. At GV stage, IP3R1 are arranged as a network throughout the cytoplasm with minute accumulation around the nucleus. At MII stage, IP3R1 diffuses to the entire cytoplasm in a more reticular manner, and obvious clusters of IP3R1 are observed at the cortex of the egg. This structural reorganization provides acquisition of [Ca(2+)](i) oscillatory activity during fertilization. In this review, general properties of IP3R1 in somatic cells and mammalian oocyte are introduced. Korean Society of Developmental Biology 2019-03 2019-03-31 /pmc/articles/PMC6487317/ /pubmed/31049467 http://dx.doi.org/10.12717/DR.2019.23.1.001 Text en © Copyright 2019 The Korean Society of Developmental Biology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Yoon, Sook Young
Role of Type 1 Inositol 1,4,5-triphosphate Receptors in Mammalian Oocytes
title Role of Type 1 Inositol 1,4,5-triphosphate Receptors in Mammalian Oocytes
title_full Role of Type 1 Inositol 1,4,5-triphosphate Receptors in Mammalian Oocytes
title_fullStr Role of Type 1 Inositol 1,4,5-triphosphate Receptors in Mammalian Oocytes
title_full_unstemmed Role of Type 1 Inositol 1,4,5-triphosphate Receptors in Mammalian Oocytes
title_short Role of Type 1 Inositol 1,4,5-triphosphate Receptors in Mammalian Oocytes
title_sort role of type 1 inositol 1,4,5-triphosphate receptors in mammalian oocytes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6487317/
https://www.ncbi.nlm.nih.gov/pubmed/31049467
http://dx.doi.org/10.12717/DR.2019.23.1.001
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