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Environmental Pollutant Benzo[a]pyrene Induces Recurrent Pregnancy Loss through Promoting Apoptosis and Suppressing Migration of Extravillous Trophoblast

METHODS: The implantation sites, fetus resorption, and abnormal fetuses were studied in pregnant mice treated with different doses of BaP by oral gavage from day 1 to day 10 of gestation. Additionally, apoptosis and related signaling pathway, and the migration and invasion of trophoblasts, were asse...

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Autores principales: Ye, Yang, Jiang, Sushi, Zhang, Chao, Cheng, Yanxiang, Zhong, Huan, Du, Tao, Xu, Wenming, Azziz, Ricardo, Zhang, Huidong, Zhao, Xiaomiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586159/
https://www.ncbi.nlm.nih.gov/pubmed/33123590
http://dx.doi.org/10.1155/2020/8983494
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author Ye, Yang
Jiang, Sushi
Zhang, Chao
Cheng, Yanxiang
Zhong, Huan
Du, Tao
Xu, Wenming
Azziz, Ricardo
Zhang, Huidong
Zhao, Xiaomiao
author_facet Ye, Yang
Jiang, Sushi
Zhang, Chao
Cheng, Yanxiang
Zhong, Huan
Du, Tao
Xu, Wenming
Azziz, Ricardo
Zhang, Huidong
Zhao, Xiaomiao
author_sort Ye, Yang
collection PubMed
description METHODS: The implantation sites, fetus resorption, and abnormal fetuses were studied in pregnant mice treated with different doses of BaP by oral gavage from day 1 to day 10 of gestation. Additionally, apoptosis and related signaling pathway, and the migration and invasion of trophoblasts, were assessed before and after exposure of BPDE in Swan 71 trophoblast cell. Besides, the migration and invasion, and its related signaling pathway, were assessed in villi obtained from women. RESULTS: We observed a concentration-dependent incidence of abnormal murine fetuses, beginning with 0.1 mg/kg BaP; with a BaP concentration of 2 mg/kg, no fetuses developed. Correspondingly, a BPDE concentration-dependent apoptosis of human trophoblasts. Beginning with 0.5 μM BPDE exposure, Bax/Caspase-3 were increased and Bcl-2 decreased. Furthermore, BPDE also inhibited, in a dose-dependent manner, the migration of villous explants from elective abortion women, consistent with the reduced migration of villous explants from women with recurrent pregnancy loss (RPL), and reduced the cell immigration in Swan 71 trophoblasts, in a dose-dependent manner measured by transwell assays. CONCLUSIONS: Our study results provide mechanistic insight to the effect of BPDE on trophoblast dysfunction through enhanced cell apoptosis and inhibited migration, providing further experimental evidence to the causative links between BaP exposure and PRL.
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spelling pubmed-75861592020-10-28 Environmental Pollutant Benzo[a]pyrene Induces Recurrent Pregnancy Loss through Promoting Apoptosis and Suppressing Migration of Extravillous Trophoblast Ye, Yang Jiang, Sushi Zhang, Chao Cheng, Yanxiang Zhong, Huan Du, Tao Xu, Wenming Azziz, Ricardo Zhang, Huidong Zhao, Xiaomiao Biomed Res Int Research Article METHODS: The implantation sites, fetus resorption, and abnormal fetuses were studied in pregnant mice treated with different doses of BaP by oral gavage from day 1 to day 10 of gestation. Additionally, apoptosis and related signaling pathway, and the migration and invasion of trophoblasts, were assessed before and after exposure of BPDE in Swan 71 trophoblast cell. Besides, the migration and invasion, and its related signaling pathway, were assessed in villi obtained from women. RESULTS: We observed a concentration-dependent incidence of abnormal murine fetuses, beginning with 0.1 mg/kg BaP; with a BaP concentration of 2 mg/kg, no fetuses developed. Correspondingly, a BPDE concentration-dependent apoptosis of human trophoblasts. Beginning with 0.5 μM BPDE exposure, Bax/Caspase-3 were increased and Bcl-2 decreased. Furthermore, BPDE also inhibited, in a dose-dependent manner, the migration of villous explants from elective abortion women, consistent with the reduced migration of villous explants from women with recurrent pregnancy loss (RPL), and reduced the cell immigration in Swan 71 trophoblasts, in a dose-dependent manner measured by transwell assays. CONCLUSIONS: Our study results provide mechanistic insight to the effect of BPDE on trophoblast dysfunction through enhanced cell apoptosis and inhibited migration, providing further experimental evidence to the causative links between BaP exposure and PRL. Hindawi 2020-10-16 /pmc/articles/PMC7586159/ /pubmed/33123590 http://dx.doi.org/10.1155/2020/8983494 Text en Copyright © 2020 Yang Ye et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ye, Yang
Jiang, Sushi
Zhang, Chao
Cheng, Yanxiang
Zhong, Huan
Du, Tao
Xu, Wenming
Azziz, Ricardo
Zhang, Huidong
Zhao, Xiaomiao
Environmental Pollutant Benzo[a]pyrene Induces Recurrent Pregnancy Loss through Promoting Apoptosis and Suppressing Migration of Extravillous Trophoblast
title Environmental Pollutant Benzo[a]pyrene Induces Recurrent Pregnancy Loss through Promoting Apoptosis and Suppressing Migration of Extravillous Trophoblast
title_full Environmental Pollutant Benzo[a]pyrene Induces Recurrent Pregnancy Loss through Promoting Apoptosis and Suppressing Migration of Extravillous Trophoblast
title_fullStr Environmental Pollutant Benzo[a]pyrene Induces Recurrent Pregnancy Loss through Promoting Apoptosis and Suppressing Migration of Extravillous Trophoblast
title_full_unstemmed Environmental Pollutant Benzo[a]pyrene Induces Recurrent Pregnancy Loss through Promoting Apoptosis and Suppressing Migration of Extravillous Trophoblast
title_short Environmental Pollutant Benzo[a]pyrene Induces Recurrent Pregnancy Loss through Promoting Apoptosis and Suppressing Migration of Extravillous Trophoblast
title_sort environmental pollutant benzo[a]pyrene induces recurrent pregnancy loss through promoting apoptosis and suppressing migration of extravillous trophoblast
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586159/
https://www.ncbi.nlm.nih.gov/pubmed/33123590
http://dx.doi.org/10.1155/2020/8983494
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