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

Author:

Chen Yun1ORCID,Ou Zihao2ORCID,Pang Menglan1,Tao Zixin1ORCID,Zheng Xifen3,Huang Zhipeng1,Wen Dongni1,Li Qianbei2,Zhou Ruisi1,Chen Peng4,Situ Bo2,Sheng Chao1,Huang Yingying1,Yue Xiaojing1,Zheng Lei2ORCID,Huang Liping1

Affiliation:

1. Department of Obstetrics and Gynecology Nanfang Hospital, Southern Medical University Guangzhou Guangdong China

2. Department of Laboratory Medicine Nanfang Hospital, Southern Medical University Guangzhou Guangdong China

3. Department of Laboratory Medicine Zhujiang Hospital, Southern Medical University Guangzhou Guangdong China

4. Department of Pathophysiology, Guangdong Provincial Key Laboratory of Proteomics, School of Basic Medical Sciences Southern Medical University Guangzhou Guangdong China

Abstract

AbstractPreeclampsia (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.

Funder

National Science Fund for Distinguished Young Scholars

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Publisher

Wiley

Subject

Cell Biology,Histology

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