RIPK1 inhibition reduces biliary injury and fibrosis in primary sclerosing cholangitis

Primary sclerosing cholangitis (PSC) is a chronic cholestatic liver disease with no effective curative therapies. Necroptosis, a regulated necrotic cell death pathway controlled by receptor-interacting protein kinase 1 (RIPK1), has emerged as a potential driver of inflammation and fibrosis in chronic liver disorders. We investigated the role of necroptosis in PSC and whether RIPK1 inhibition could modify disease course and progression. Spatial profiling of human PSC biopsies revealed that necroptosis primarily affects cholangiocytes, while apoptosis was more frequent in hepatocytes and nonbiliary cells. In vitro, necroptosis inhibition protected cholangiocytes, and <i>RIPK1</i> deletion conferred resistance to TNF-mediated cytotoxicity. In a murine model of PSC, pharmacological RIPK1 inhibition reduced cholestatic injury, hepatic inflammation, and biliary fibrosis. Multiomic analyses comprehensively demonstrated reprogramming toward wild-type-like profiles following treatment. These findings identify necroptosis as a critical effector in PSC and highlight RIPK1 inhibition as a promising disease-modifying approach, opening the door to targeted necroptosis-based therapies for this otherwise untreatable disease.

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Publication Details

Journal
Science Advances
Published
2025-12-17
DOI
https://doi.org/10.1126/sciadv.adz7907
Primary Topic
Liver Diseases and Immunity
Type
article
Field-Weighted Citation Impact
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article

RIPK1 inhibition reduces biliary injury and fibrosis in primary sclerosing cholangitis

Inès Metatla, Siham Benyahia, Laetitia Dinard, Maharajah Ponnaiah et al.
Science Advances
Liver Diseases and Immunity
article

RIPK1 inhibition reduces biliary injury and fibrosis in primary sclerosing cholangitis

Inès Metatla, Siham Benyahia, Laetitia Dinard, Maharajah Ponnaiah, Sara Lemoinne, Marie Lhomme, Pierre‐Antoine Soret, Dominique Wendum, Chantal Housset, J. Delaunay, Tounsia Aït‐Slimane, Tatiana Ledent, Virginie Steunou, Valéria Pistorio, Lawrence Serfaty, Jérémie Gautheron, Axelle Cadoret, Amine Majdi, Jérôme Galon, Vlad Ratziu, Franck Verdonk, Juliette Tokgozoglu, Julien Hédou, Ida Chiara Guerrera, Nicolas Chignard, Christophe Corpechot, Patrick Soussan, O. Chazouillères, Nadia Darwane
article en

Abstract

Primary sclerosing cholangitis (PSC) is a chronic cholestatic liver disease with no effective curative therapies. Necroptosis, a regulated necrotic cell death pathway controlled by receptor-interacting protein kinase 1 (RIPK1), has emerged as a potential driver of inflammation and fibrosis in chronic liver disorders. We investigated the role of necroptosis in PSC and whether RIPK1 inhibition could modify disease course and progression. Spatial profiling of human PSC biopsies revealed that necroptosis primarily affects cholangiocytes, while apoptosis was more frequent in hepatocytes and nonbiliary cells. In vitro, necroptosis inhibition protected cholangiocytes, and <i>RIPK1</i> deletion conferred resistance to TNF-mediated cytotoxicity. In a murine model of PSC, pharmacological RIPK1 inhibition reduced cholestatic injury, hepatic inflammation, and biliary fibrosis. Multiomic analyses comprehensively demonstrated reprogramming toward wild-type-like profiles following treatment. These findings identify necroptosis as a critical effector in PSC and highlight RIPK1 inhibition as a promising disease-modifying approach, opening the door to targeted necroptosis-based therapies for this otherwise untreatable disease.

Science AdvancesVol. 11(51)
Délégation Paris 5 (FR), Inserm (FR), Université Paris Cité (FR), Sorbonne Université (FR), Centre de Recherche des Cordeliers (FR), Assistance Publique – Hôpitaux de Paris (FR), Hôpital Saint-Antoine (FR), Fédération Hospitalo-Universitaire, Paris Center for Microbiome Medicine (FR), Centre de Recherche Saint-Antoine (FR), Fondation pour l’innovation en Cadiométabolisme et Nutrition (FR)
Openalex Percentile: Top 46%
Liver Diseases and Immunity
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