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WNT signaling contributes to the extrahepatic bile duct proliferative response to obstruction in mice

Title: WNT signaling contributes to the extrahepatic bile duct proliferative response to obstruction in mice
Authors: Ashley N. Calder; Mirabelle Q. Peter; John W. Tobias; Nureen H. Mohamad Zaki; Theresa M. Keeley; Timothy L. Frankel; Linda C. Samuelson; Nataliya Razumilava
Source: JCI Insight, Vol 10, Iss 2 (2025)
Publisher Information: American Society for Clinical investigation
Publication Year: 2025
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: Hepatology; Medicine
Description: Biliary obstruction and cholangiocyte hyperproliferation are important features of cholangiopathies affecting the large extrahepatic bile duct (EHBD). The mechanisms underlying obstruction-induced cholangiocyte proliferation in the EHBD remain poorly understood. Developmental pathways, including WNT signaling, are implicated in regulating injury responses in many tissues, including the liver. To investigate the contribution of WNT signaling to obstruction-induced cholangiocyte proliferation in the EHBD, we used complementary in vivo and in vitro models with pharmacologic interventions and transcriptomic analyses. To model obstruction, we used bile duct ligation (BDL) in mice. Human and mouse biliary organoids and mouse biliary explants were used to investigate the effects of WNT activation and inhibition in vitro. We observed an upregulation of WNT ligand expression associated with increased biliary proliferation following obstruction. Cholangiocytes were identified as both WNT ligand–expressing and WNT-responsive cells. Inhibition of WNT signaling decreased cholangiocyte proliferation in vivo and in vitro, while activation increased proliferation. WNT effects on cholangiocyte proliferation were β-catenin dependent, and we showed a direct effect of WNT7B on cholangiocyte growth. Our studies suggested that cholangiocyte-derived WNT ligands can activate WNT signaling to induce proliferation after obstructive injury. These findings implicate the WNT pathway in injury-induced cholangiocyte proliferation within the EHBD.
Document Type: article in journal/newspaper
Language: English
Relation: https://doi.org/10.1172/jci.insight.181857; https://doaj.org/toc/2379-3708; https://doaj.org/article/4dbd56dce6b243de97ebf480b649ea31
Availability: https://doaj.org/article/4dbd56dce6b243de97ebf480b649ea31
Accession Number: edsbas.F9276F3F
Database: BASE