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Animal models of the placenta accreta spectrum: current status and further perspectives
Placenta accreta spectrum disorder (PAS) is a kind of disease of placentation defined as abnormal trophoblast invasion of part or all of the placenta into the myometrium, even penetrating the uterus. Decidual deficiency, abnormal vascular remodeling in the maternal–fetal interface, and excessive inv...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10200980/ https://www.ncbi.nlm.nih.gov/pubmed/37223034 http://dx.doi.org/10.3389/fendo.2023.1118168 |
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author | Ma, Yongdan Hu, Yongyan Ma, Jingmei |
author_facet | Ma, Yongdan Hu, Yongyan Ma, Jingmei |
author_sort | Ma, Yongdan |
collection | PubMed |
description | Placenta accreta spectrum disorder (PAS) is a kind of disease of placentation defined as abnormal trophoblast invasion of part or all of the placenta into the myometrium, even penetrating the uterus. Decidual deficiency, abnormal vascular remodeling in the maternal–fetal interface, and excessive invasion by extravillous trophoblast (EVT) cells contribute to its onset. However, the mechanisms and signaling pathways underlying such phenotypes are not fully understood, partly due to the lack of suitable experimental animal models. Appropriate animal models will facilitate the comprehensive and systematic elucidation of the pathogenesis of PAS. Due to the remarkably similar functional placental villous units and hemochorial placentation to humans, the current animal models of PAS are based on mice. There are various mouse models induced by uterine surgery to simulate different phenotypes of PAS, such as excessive invasion of EVT or immune disturbance at the maternal–fetal interface, which could define the pathological mechanism of PAS from the perspective of the “soil.” Additionally, genetically modified mouse models could be used to study PAS, which is helpful to exploring the pathogenesis of PAS from the perspectives of both “soil” and “seed,” respectively. This review details early placental development in mice, with a focus on the approaches of PAS modeling. Additionally, the strengths, limitations and the applicability of each strategy and further perspectives are summarized to provide the theoretical foundation for researchers to select appropriate animal models for various research purposes. This will help better determine the pathogenesis of PAS and even promote possible therapy. |
format | Online Article Text |
id | pubmed-10200980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102009802023-05-23 Animal models of the placenta accreta spectrum: current status and further perspectives Ma, Yongdan Hu, Yongyan Ma, Jingmei Front Endocrinol (Lausanne) Endocrinology Placenta accreta spectrum disorder (PAS) is a kind of disease of placentation defined as abnormal trophoblast invasion of part or all of the placenta into the myometrium, even penetrating the uterus. Decidual deficiency, abnormal vascular remodeling in the maternal–fetal interface, and excessive invasion by extravillous trophoblast (EVT) cells contribute to its onset. However, the mechanisms and signaling pathways underlying such phenotypes are not fully understood, partly due to the lack of suitable experimental animal models. Appropriate animal models will facilitate the comprehensive and systematic elucidation of the pathogenesis of PAS. Due to the remarkably similar functional placental villous units and hemochorial placentation to humans, the current animal models of PAS are based on mice. There are various mouse models induced by uterine surgery to simulate different phenotypes of PAS, such as excessive invasion of EVT or immune disturbance at the maternal–fetal interface, which could define the pathological mechanism of PAS from the perspective of the “soil.” Additionally, genetically modified mouse models could be used to study PAS, which is helpful to exploring the pathogenesis of PAS from the perspectives of both “soil” and “seed,” respectively. This review details early placental development in mice, with a focus on the approaches of PAS modeling. Additionally, the strengths, limitations and the applicability of each strategy and further perspectives are summarized to provide the theoretical foundation for researchers to select appropriate animal models for various research purposes. This will help better determine the pathogenesis of PAS and even promote possible therapy. Frontiers Media S.A. 2023-05-08 /pmc/articles/PMC10200980/ /pubmed/37223034 http://dx.doi.org/10.3389/fendo.2023.1118168 Text en Copyright © 2023 Ma, Hu and Ma 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 | Endocrinology Ma, Yongdan Hu, Yongyan Ma, Jingmei Animal models of the placenta accreta spectrum: current status and further perspectives |
title | Animal models of the placenta accreta spectrum: current status and further perspectives |
title_full | Animal models of the placenta accreta spectrum: current status and further perspectives |
title_fullStr | Animal models of the placenta accreta spectrum: current status and further perspectives |
title_full_unstemmed | Animal models of the placenta accreta spectrum: current status and further perspectives |
title_short | Animal models of the placenta accreta spectrum: current status and further perspectives |
title_sort | animal models of the placenta accreta spectrum: current status and further perspectives |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10200980/ https://www.ncbi.nlm.nih.gov/pubmed/37223034 http://dx.doi.org/10.3389/fendo.2023.1118168 |
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