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Microbiome-derived secondary bile acids promote repair of colonic mucosa after injury

2025/03/21 by Brecht Attema, Folkert Kuipers · 1 voice
Medicine · #Amoebic Infections and Treatments #Pancreatitis Pathology and Treatment #Pancreatic and Hepatic Oncology Research

paper · pdf · doi:10.1038/s44321-025-00218-2

openalex publication_date 2025/03/21 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/31

Abstract

Dysbiosis, i.e., an imbalance in the composition of the intestinal microbiome, has been linked to the etiology of inflammatory bowel diseases (IBD). Secondary bile acids (BAs) are microbiome-derived metabolites increasingly recognized for their important signaling functions in host (patho)physiology. In this issue of EMBO Molecular Medicine, Jalil et al (Jalil et al, 2025) report that increased production of secondary BAs upon administration of the human bacterium Clostridium scindens (C. scindens) improves colonic health in mice with chemically-induced colitis via activation of the membrane bound BA receptor TGR5. These findings indicate an important role for secondary BA signaling in colon mucosal healing upon injury and suggest that modulation of microbiome composition could serve as a therapeutic approach for patients with IBD. B. Attema and F. Kuipers discuss a recent study by Schoonjans and colleagues(in this issue of EMBO Mol Med) that reveals the important role of secondary bile acid signaling in colon mucosal healing after injury.

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