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Placental Abnormalities are Associated With Specific Windows of Embryo Culture in a Mouse Model

Assisted Reproductive Technologies (ART) employ gamete/embryo handling and culture in vitro to produce offspring. ART pregnancies have an increased risk of low birth weight, abnormal placentation, pregnancy complications, and imprinting disorders. Embryo culture induces low birth weight, abnormal pl...

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Autores principales: Vrooman, Lisa A., Rhon-Calderon, Eric A., Suri, Kashviya V., Dahiya, Asha K., Lan, Yemin, Schultz, Richard M., Bartolomei, Marisa S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081528/
https://www.ncbi.nlm.nih.gov/pubmed/35547813
http://dx.doi.org/10.3389/fcell.2022.884088
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author Vrooman, Lisa A.
Rhon-Calderon, Eric A.
Suri, Kashviya V.
Dahiya, Asha K.
Lan, Yemin
Schultz, Richard M.
Bartolomei, Marisa S.
author_facet Vrooman, Lisa A.
Rhon-Calderon, Eric A.
Suri, Kashviya V.
Dahiya, Asha K.
Lan, Yemin
Schultz, Richard M.
Bartolomei, Marisa S.
author_sort Vrooman, Lisa A.
collection PubMed
description Assisted Reproductive Technologies (ART) employ gamete/embryo handling and culture in vitro to produce offspring. ART pregnancies have an increased risk of low birth weight, abnormal placentation, pregnancy complications, and imprinting disorders. Embryo culture induces low birth weight, abnormal placental morphology, and lower levels of DNA methylation in placentas in a mouse model of ART. Whether preimplantation embryos at specific stages of development are more susceptible to these perturbations remains unresolved. Accordingly, we performed embryo culture for several discrete periods of preimplantation development and following embryo transfer, assessed fetal and placental outcomes at term. We observed a reduction in fetal:placental ratio associated with two distinct windows of preimplantation embryo development, one prior to the morula stage and the other from the morula to blastocyst stage, whereas placental morphological abnormalities and reduced imprinting control region methylation were only associated with culture prior to the morula stage. Extended culture to the blastocyst stage also induces additional placental DNA methylation changes compared to embryos transferred at the morula stage, and female concepti exhibited a higher loss of DNA methylation than males. By identifying specific developmental windows of susceptibility, this study provides a framework to optimize further culture conditions to minimize risks associated with ART pregnancies.
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spelling pubmed-90815282022-05-10 Placental Abnormalities are Associated With Specific Windows of Embryo Culture in a Mouse Model Vrooman, Lisa A. Rhon-Calderon, Eric A. Suri, Kashviya V. Dahiya, Asha K. Lan, Yemin Schultz, Richard M. Bartolomei, Marisa S. Front Cell Dev Biol Cell and Developmental Biology Assisted Reproductive Technologies (ART) employ gamete/embryo handling and culture in vitro to produce offspring. ART pregnancies have an increased risk of low birth weight, abnormal placentation, pregnancy complications, and imprinting disorders. Embryo culture induces low birth weight, abnormal placental morphology, and lower levels of DNA methylation in placentas in a mouse model of ART. Whether preimplantation embryos at specific stages of development are more susceptible to these perturbations remains unresolved. Accordingly, we performed embryo culture for several discrete periods of preimplantation development and following embryo transfer, assessed fetal and placental outcomes at term. We observed a reduction in fetal:placental ratio associated with two distinct windows of preimplantation embryo development, one prior to the morula stage and the other from the morula to blastocyst stage, whereas placental morphological abnormalities and reduced imprinting control region methylation were only associated with culture prior to the morula stage. Extended culture to the blastocyst stage also induces additional placental DNA methylation changes compared to embryos transferred at the morula stage, and female concepti exhibited a higher loss of DNA methylation than males. By identifying specific developmental windows of susceptibility, this study provides a framework to optimize further culture conditions to minimize risks associated with ART pregnancies. Frontiers Media S.A. 2022-04-25 /pmc/articles/PMC9081528/ /pubmed/35547813 http://dx.doi.org/10.3389/fcell.2022.884088 Text en Copyright © 2022 Vrooman, Rhon-Calderon, Suri, Dahiya, Lan, Schultz and Bartolomei. 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
Vrooman, Lisa A.
Rhon-Calderon, Eric A.
Suri, Kashviya V.
Dahiya, Asha K.
Lan, Yemin
Schultz, Richard M.
Bartolomei, Marisa S.
Placental Abnormalities are Associated With Specific Windows of Embryo Culture in a Mouse Model
title Placental Abnormalities are Associated With Specific Windows of Embryo Culture in a Mouse Model
title_full Placental Abnormalities are Associated With Specific Windows of Embryo Culture in a Mouse Model
title_fullStr Placental Abnormalities are Associated With Specific Windows of Embryo Culture in a Mouse Model
title_full_unstemmed Placental Abnormalities are Associated With Specific Windows of Embryo Culture in a Mouse Model
title_short Placental Abnormalities are Associated With Specific Windows of Embryo Culture in a Mouse Model
title_sort placental abnormalities are associated with specific windows of embryo culture in a mouse model
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081528/
https://www.ncbi.nlm.nih.gov/pubmed/35547813
http://dx.doi.org/10.3389/fcell.2022.884088
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