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Regulation of Oocyte Apoptosis: A View from Gene Knockout Mice

Apoptosis is a form of programmed cell death that plays a critical role in cellular homeostasis and development, including in the ovarian reserve. In humans, hundreds of thousands of oocytes are produced in the fetal ovary. However, the majority die by apoptosis before birth. After puberty, primordi...

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Detalles Bibliográficos
Autores principales: Kaur, Sandeep, Kurokawa, Manabu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9861590/
https://www.ncbi.nlm.nih.gov/pubmed/36674865
http://dx.doi.org/10.3390/ijms24021345
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author Kaur, Sandeep
Kurokawa, Manabu
author_facet Kaur, Sandeep
Kurokawa, Manabu
author_sort Kaur, Sandeep
collection PubMed
description Apoptosis is a form of programmed cell death that plays a critical role in cellular homeostasis and development, including in the ovarian reserve. In humans, hundreds of thousands of oocytes are produced in the fetal ovary. However, the majority die by apoptosis before birth. After puberty, primordial follicles develop into mature follicles. While only a large dominant follicle is selected to ovulate, smaller ones undergo apoptosis. Despite numerous studies, the mechanism of oocyte death at the molecular level remains elusive. Over the last two and a half decades, many knockout mouse models disrupting key genes in the apoptosis pathway have been generated. In this review, we highlight some of the phenotypes and discuss distinct and overlapping roles of the apoptosis regulators in oocyte death and survival. We also review how the transcription factor p63 and its family members may trigger oocyte apoptosis in response to DNA damage.
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spelling pubmed-98615902023-01-22 Regulation of Oocyte Apoptosis: A View from Gene Knockout Mice Kaur, Sandeep Kurokawa, Manabu Int J Mol Sci Review Apoptosis is a form of programmed cell death that plays a critical role in cellular homeostasis and development, including in the ovarian reserve. In humans, hundreds of thousands of oocytes are produced in the fetal ovary. However, the majority die by apoptosis before birth. After puberty, primordial follicles develop into mature follicles. While only a large dominant follicle is selected to ovulate, smaller ones undergo apoptosis. Despite numerous studies, the mechanism of oocyte death at the molecular level remains elusive. Over the last two and a half decades, many knockout mouse models disrupting key genes in the apoptosis pathway have been generated. In this review, we highlight some of the phenotypes and discuss distinct and overlapping roles of the apoptosis regulators in oocyte death and survival. We also review how the transcription factor p63 and its family members may trigger oocyte apoptosis in response to DNA damage. MDPI 2023-01-10 /pmc/articles/PMC9861590/ /pubmed/36674865 http://dx.doi.org/10.3390/ijms24021345 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 Review
Kaur, Sandeep
Kurokawa, Manabu
Regulation of Oocyte Apoptosis: A View from Gene Knockout Mice
title Regulation of Oocyte Apoptosis: A View from Gene Knockout Mice
title_full Regulation of Oocyte Apoptosis: A View from Gene Knockout Mice
title_fullStr Regulation of Oocyte Apoptosis: A View from Gene Knockout Mice
title_full_unstemmed Regulation of Oocyte Apoptosis: A View from Gene Knockout Mice
title_short Regulation of Oocyte Apoptosis: A View from Gene Knockout Mice
title_sort regulation of oocyte apoptosis: a view from gene knockout mice
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9861590/
https://www.ncbi.nlm.nih.gov/pubmed/36674865
http://dx.doi.org/10.3390/ijms24021345
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