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Advanced Maternal Age Deteriorates the Developmental Competence of Vitrified Oocytes in Mice

Advanced maternal age (AMA) is known to be related to the decrease in the quality and quantity of oocytes. Oocyte vitrification is now considered an established assisted reproductive technology for fertility preservation. However, it remains unclear whether the oocytes in older women are more sensit...

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Autores principales: Lee, Ju Hee, Park, Jae Kyun, Yoon, Sook Young, Park, Eun A, Jun, Jin Hyun, Lim, Hyunjung J., Kim, Jayeon, Song, Haengseok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234289/
https://www.ncbi.nlm.nih.gov/pubmed/34205802
http://dx.doi.org/10.3390/cells10061563
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author Lee, Ju Hee
Park, Jae Kyun
Yoon, Sook Young
Park, Eun A
Jun, Jin Hyun
Lim, Hyunjung J.
Kim, Jayeon
Song, Haengseok
author_facet Lee, Ju Hee
Park, Jae Kyun
Yoon, Sook Young
Park, Eun A
Jun, Jin Hyun
Lim, Hyunjung J.
Kim, Jayeon
Song, Haengseok
author_sort Lee, Ju Hee
collection PubMed
description Advanced maternal age (AMA) is known to be related to the decrease in the quality and quantity of oocytes. Oocyte vitrification is now considered an established assisted reproductive technology for fertility preservation. However, it remains unclear whether the oocytes in older women are more sensitive to various insults during vitrification. Thus, we evaluated whether AMA affects cellular and molecular features and developmental outcomes of oocytes after vitrification in mice. The oocytes were grouped as young fresh (YF), young vitrified/warmed (YV), aged fresh (AF), and aged vitrified/warmed (AV). The survival rate of AV oocytes was significantly lower than that of YV oocytes. The rates of fertilization, cleavage, and blastocyst formation of AV oocytes were significantly lower than those of other groups. AV oocytes were represented as aberrations in mitochondria distribution, microvacuole size, and autophagosome formation, leading to delayed embryo development in mice. This delay was associated with a reduced number of total cells and trophectoderm in the blastocyst developed from AV oocytes. Collectively, AMA exaggerates the vulnerability of oocytes to cryo-damage that occurs during vitrification in mice, suggesting that the current vitrification protocols optimized for oocytes from young females should be modified for oocytes from aged women.
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spelling pubmed-82342892021-06-27 Advanced Maternal Age Deteriorates the Developmental Competence of Vitrified Oocytes in Mice Lee, Ju Hee Park, Jae Kyun Yoon, Sook Young Park, Eun A Jun, Jin Hyun Lim, Hyunjung J. Kim, Jayeon Song, Haengseok Cells Article Advanced maternal age (AMA) is known to be related to the decrease in the quality and quantity of oocytes. Oocyte vitrification is now considered an established assisted reproductive technology for fertility preservation. However, it remains unclear whether the oocytes in older women are more sensitive to various insults during vitrification. Thus, we evaluated whether AMA affects cellular and molecular features and developmental outcomes of oocytes after vitrification in mice. The oocytes were grouped as young fresh (YF), young vitrified/warmed (YV), aged fresh (AF), and aged vitrified/warmed (AV). The survival rate of AV oocytes was significantly lower than that of YV oocytes. The rates of fertilization, cleavage, and blastocyst formation of AV oocytes were significantly lower than those of other groups. AV oocytes were represented as aberrations in mitochondria distribution, microvacuole size, and autophagosome formation, leading to delayed embryo development in mice. This delay was associated with a reduced number of total cells and trophectoderm in the blastocyst developed from AV oocytes. Collectively, AMA exaggerates the vulnerability of oocytes to cryo-damage that occurs during vitrification in mice, suggesting that the current vitrification protocols optimized for oocytes from young females should be modified for oocytes from aged women. MDPI 2021-06-21 /pmc/articles/PMC8234289/ /pubmed/34205802 http://dx.doi.org/10.3390/cells10061563 Text en © 2021 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
Lee, Ju Hee
Park, Jae Kyun
Yoon, Sook Young
Park, Eun A
Jun, Jin Hyun
Lim, Hyunjung J.
Kim, Jayeon
Song, Haengseok
Advanced Maternal Age Deteriorates the Developmental Competence of Vitrified Oocytes in Mice
title Advanced Maternal Age Deteriorates the Developmental Competence of Vitrified Oocytes in Mice
title_full Advanced Maternal Age Deteriorates the Developmental Competence of Vitrified Oocytes in Mice
title_fullStr Advanced Maternal Age Deteriorates the Developmental Competence of Vitrified Oocytes in Mice
title_full_unstemmed Advanced Maternal Age Deteriorates the Developmental Competence of Vitrified Oocytes in Mice
title_short Advanced Maternal Age Deteriorates the Developmental Competence of Vitrified Oocytes in Mice
title_sort advanced maternal age deteriorates the developmental competence of vitrified oocytes in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234289/
https://www.ncbi.nlm.nih.gov/pubmed/34205802
http://dx.doi.org/10.3390/cells10061563
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