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Extracellular vesicles derived from Akkermansia muciniphila promote placentation and mitigate preeclampsia in a mouse model

Preeclampsia (PE) is a multisystem disorder with high maternal morbidity and mortality rates. Currently, no practical therapeutic approach is available to prevent PE progression, except for early delivery. Gut dysbiosis is associated with PE development. Previous data showed that the abundance of Ak...

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Autores principales: Chen, Yun, Ou, Zihao, Pang, Menglan, Tao, Zixin, Zheng, Xifen, Huang, Zhipeng, Wen, Dongni, Li, Qianbei, Zhou, Ruisi, Chen, Peng, Situ, Bo, Sheng, Chao, Huang, Yingying, Yue, Xiaojing, Zheng, Lei, Huang, Liping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173384/
https://www.ncbi.nlm.nih.gov/pubmed/37165987
http://dx.doi.org/10.1002/jev2.12328
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author Chen, Yun
Ou, Zihao
Pang, Menglan
Tao, Zixin
Zheng, Xifen
Huang, Zhipeng
Wen, Dongni
Li, Qianbei
Zhou, Ruisi
Chen, Peng
Situ, Bo
Sheng, Chao
Huang, Yingying
Yue, Xiaojing
Zheng, Lei
Huang, Liping
author_facet Chen, Yun
Ou, Zihao
Pang, Menglan
Tao, Zixin
Zheng, Xifen
Huang, Zhipeng
Wen, Dongni
Li, Qianbei
Zhou, Ruisi
Chen, Peng
Situ, Bo
Sheng, Chao
Huang, Yingying
Yue, Xiaojing
Zheng, Lei
Huang, Liping
author_sort Chen, Yun
collection PubMed
description Preeclampsia (PE) is a multisystem disorder with high maternal morbidity and mortality rates. Currently, no practical therapeutic approach is available to prevent PE progression, except for early delivery. Gut dysbiosis is associated with PE development. Previous data showed that the abundance of Akkermansia muciniphila (Am) was lower in patients with PE than in normotensive pregnant women. Here, in this study, decreased abundance of Am was observed in a PE mouse model. Also, we found that administration with Am could significantly attenuate systolic blood pressure, promote foetal growth and improve the placental pathology in mice with PE. Moreover, Am‐derived extracellular vesicles (AmEVs) were transferred from the gastrointestinal (GI) tract to the placenta and mitigated pre‐eclamptic symptoms in PE mice. These beneficial effects of AmEVs were mediated by enhanced trophoblast invasion of the spiral artery (SpA) and SpA remodelling through activation of the epidermal growth factor receptor (EGFR)–phosphatidylinositol‐3‐kinase (PI3K)–protein kinase B (AKT) signalling pathway. Collectively, our findings revealed the potential benefit of using AmEVs for PE treatment and highlighted important host–microbiota interactions.
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spelling pubmed-101733842023-05-12 Extracellular vesicles derived from Akkermansia muciniphila promote placentation and mitigate preeclampsia in a mouse model Chen, Yun Ou, Zihao Pang, Menglan Tao, Zixin Zheng, Xifen Huang, Zhipeng Wen, Dongni Li, Qianbei Zhou, Ruisi Chen, Peng Situ, Bo Sheng, Chao Huang, Yingying Yue, Xiaojing Zheng, Lei Huang, Liping J Extracell Vesicles Research Articles Preeclampsia (PE) is a multisystem disorder with high maternal morbidity and mortality rates. Currently, no practical therapeutic approach is available to prevent PE progression, except for early delivery. Gut dysbiosis is associated with PE development. Previous data showed that the abundance of Akkermansia muciniphila (Am) was lower in patients with PE than in normotensive pregnant women. Here, in this study, decreased abundance of Am was observed in a PE mouse model. Also, we found that administration with Am could significantly attenuate systolic blood pressure, promote foetal growth and improve the placental pathology in mice with PE. Moreover, Am‐derived extracellular vesicles (AmEVs) were transferred from the gastrointestinal (GI) tract to the placenta and mitigated pre‐eclamptic symptoms in PE mice. These beneficial effects of AmEVs were mediated by enhanced trophoblast invasion of the spiral artery (SpA) and SpA remodelling through activation of the epidermal growth factor receptor (EGFR)–phosphatidylinositol‐3‐kinase (PI3K)–protein kinase B (AKT) signalling pathway. Collectively, our findings revealed the potential benefit of using AmEVs for PE treatment and highlighted important host–microbiota interactions. John Wiley and Sons Inc. 2023-05-11 2023-05 /pmc/articles/PMC10173384/ /pubmed/37165987 http://dx.doi.org/10.1002/jev2.12328 Text en © 2023 The Authors. Journal of Extracellular Vesicles published by Wiley Periodicals, LLC on behalf of the International Society for Extracellular Vesicles. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Chen, Yun
Ou, Zihao
Pang, Menglan
Tao, Zixin
Zheng, Xifen
Huang, Zhipeng
Wen, Dongni
Li, Qianbei
Zhou, Ruisi
Chen, Peng
Situ, Bo
Sheng, Chao
Huang, Yingying
Yue, Xiaojing
Zheng, Lei
Huang, Liping
Extracellular vesicles derived from Akkermansia muciniphila promote placentation and mitigate preeclampsia in a mouse model
title Extracellular vesicles derived from Akkermansia muciniphila promote placentation and mitigate preeclampsia in a mouse model
title_full Extracellular vesicles derived from Akkermansia muciniphila promote placentation and mitigate preeclampsia in a mouse model
title_fullStr Extracellular vesicles derived from Akkermansia muciniphila promote placentation and mitigate preeclampsia in a mouse model
title_full_unstemmed Extracellular vesicles derived from Akkermansia muciniphila promote placentation and mitigate preeclampsia in a mouse model
title_short Extracellular vesicles derived from Akkermansia muciniphila promote placentation and mitigate preeclampsia in a mouse model
title_sort extracellular vesicles derived from akkermansia muciniphila promote placentation and mitigate preeclampsia in a mouse model
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173384/
https://www.ncbi.nlm.nih.gov/pubmed/37165987
http://dx.doi.org/10.1002/jev2.12328
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