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The secreted protein Amuc_1409 from Akkermansia muciniphila improves gut health through intestinal stem cell regulation.

Eun-Jung KangJae-Hoon KimYoung Eun KimHana LeeKwang Bo JungDong-Ho ChangYoungjin LeeShinhye ParkEun-Young LeeEun-Ji LeeHo Bum KangMoon-Young RhyooSeungwoo SeoSohee ParkYubin HuhJun GoJung Hyeon ChoiYoung-Keun ChoiIn-Bok LeeDong-Hee ChoiYun Jeong SeoJung-Ran NohKyoung-Shim KimJung Hwan HwangJi-Seon JeongHa-Jeong KwonHee Min YooMyung Jin SonYeon-Gu KimSeung-Goo LeeTae-Young KimHyo-Jung KwonMyung Hee KimByoung-Chan KimYong-Hoon KimDukjin KangChul-Ho Lee
Published in: Nature communications (2024)
Akkermansia muciniphila has received great attention because of its beneficial roles in gut health by regulating gut immunity, promoting intestinal epithelial development, and improving barrier integrity. However, A. muciniphila-derived functional molecules regulating gut health are not well understood. Microbiome-secreted proteins act as key arbitrators of host-microbiome crosstalk through interactions with host cells in the gut and are important for understanding host-microbiome relationships. Herein, we report the biological function of Amuc_1409, a previously uncharacterised A. muciniphila-secreted protein. Amuc_1409 increased intestinal stem cell (ISC) proliferation and regeneration in ex vivo intestinal organoids and in vivo models of radiation- or chemotherapeutic drug-induced intestinal injury and natural aging with male mice. Mechanistically, Amuc_1409 promoted E-cadherin/β-catenin complex dissociation via interaction with E-cadherin, resulting in the activation of Wnt/β-catenin signaling. Our results demonstrate that Amuc_1409 plays a crucial role in intestinal homeostasis by regulating ISC activity in an E-cadherin-dependent manner and is a promising biomolecule for improving and maintaining gut health.
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