MUC17 is an essential small intestinal glycocalyx component that is disrupted in Crohn’s disease

Crohn's disease (CD) is the chronic inflammation of the terminal ileum and colon triggered by a dysregulated immune response to bacteria, but insights into specific molecular perturbations at the critical bacteria-epithelium interface are limited. Here, we report that the membrane mucin MUC17 protected small intestinal enterocytes against commensal and pathogenic bacteria. In noninflamed CD ileum, reduced MUC17 levels and a compromised glycocalyx barrier allowed recurrent bacterial contact with enterocytes. Muc17 deletion in mice rendered the small intestine particularly prone to atypical bacterial infection while maintaining resistance to colitis. The loss of Muc17 resulted in spontaneous deterioration of epithelial homeostasis and in the extraintestinal translocation of bacteria. Finally, Muc17-deficient mice harbored specific small intestinal bacterial taxa observed in patients with CD. Our findings highlight MUC17 as an essential region-specific line of defense in the small intestine with relevance for early epithelial defects in CD.

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Publication Details

Journal
JCI Insight
Published
2024-12-19
DOI
https://doi.org/10.1172/jci.insight.181481
Citations
10
Primary Topic
Inflammatory Bowel Disease
Type
article
Field-Weighted Citation Impact
5.50

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article

MUC17 is an essential small intestinal glycocalyx component that is disrupted in Crohn’s disease

Sara Thulin, Brendan Dolan, Bruce A. Vallance, Liisa Arike et al.
10 citations
JCI Insight
Inflammatory Bowel Disease
5.50
article

MUC17 is an essential small intestinal glycocalyx component that is disrupted in Crohn’s disease

Sara Thulin, Brendan Dolan, Bruce A. Vallance, Liisa Arike, Thaher Pelaseyed, Elena Layunta, Sofia Jäverfelt, Molly Sivertsson, Fleur C. van de Koolwijk
article en
10 citations

Abstract

Crohn's disease (CD) is the chronic inflammation of the terminal ileum and colon triggered by a dysregulated immune response to bacteria, but insights into specific molecular perturbations at the critical bacteria-epithelium interface are limited. Here, we report that the membrane mucin MUC17 protected small intestinal enterocytes against commensal and pathogenic bacteria. In noninflamed CD ileum, reduced MUC17 levels and a compromised glycocalyx barrier allowed recurrent bacterial contact with enterocytes. Muc17 deletion in mice rendered the small intestine particularly prone to atypical bacterial infection while maintaining resistance to colitis. The loss of Muc17 resulted in spontaneous deterioration of epithelial homeostasis and in the extraintestinal translocation of bacteria. Finally, Muc17-deficient mice harbored specific small intestinal bacterial taxa observed in patients with CD. Our findings highlight MUC17 as an essential region-specific line of defense in the small intestine with relevance for early epithelial defects in CD.

JCI InsightVol. 10(3)
University of British Columbia (CA), BC Children's Hospital (CA), University of Gothenburg (SE)
Västra Götalandsregionen, Åke Wiberg Stiftelse, Jeanssons Stiftelser, Wenner-Gren Stiftelserna, Biocodex Microbiota Foundation, Stiftelserna Wilhelm och Martina Lundgrens, Svenska Sällskapet för Medicinsk Forskning, Knut och Alice Wallenbergs Stiftelse, Vetenskapsrådet, Sahlgrenska Universitetssjukhuset, Göteborgs Universitet, Stiftelsen Clas Groschinskys Minnesfond, Science for Life Laboratory, CH.I.L.D. Foundation, National Institutes of Health, Sahlgrenska Akademin, Uppsala Multidisciplinary Center for Advanced Computational Science
Good health and well-being
Openalex Percentile: Top 4%
Inflammatory Bowel Disease
5.50
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