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Commensal bacteria weaken the intestinal barrier by suppressing epithelial neuropilin-1 and Hedgehog signaling

  • The gut microbiota influences intestinal barrier integrity through mechanisms that are incompletely understood. Here we show that the commensal microbiota weakens the intestinal barrier by suppressing epithelial neuropilin-1 (NRP1) and Hedgehog (Hh) signaling. Microbial colonization of germ-free mice dampens signaling of the intestinal Hh pathway through epithelial Toll-like receptor (TLR)-2, resulting in decreased epithelial NRP1 protein levels. Following activation via TLR2/TLR6, epithelial NRP1, a positive-feedback regulator of Hh signaling, is lysosomally degraded. Conversely, elevated epithelial NRP1 levels in germ-free mice are associated with a strengthened gut barrier. Functionally, intestinal epithelial cell-specific Nrp1 deficiency (Nrp1ΔIEC) results in decreased Hh pathway activity and a weakened gut barrier. In addition, Nrp1ΔIEC mice have a reduced density of capillary networks in their small intestinal villus structures. Collectively, our results reveal a role for theThe gut microbiota influences intestinal barrier integrity through mechanisms that are incompletely understood. Here we show that the commensal microbiota weakens the intestinal barrier by suppressing epithelial neuropilin-1 (NRP1) and Hedgehog (Hh) signaling. Microbial colonization of germ-free mice dampens signaling of the intestinal Hh pathway through epithelial Toll-like receptor (TLR)-2, resulting in decreased epithelial NRP1 protein levels. Following activation via TLR2/TLR6, epithelial NRP1, a positive-feedback regulator of Hh signaling, is lysosomally degraded. Conversely, elevated epithelial NRP1 levels in germ-free mice are associated with a strengthened gut barrier. Functionally, intestinal epithelial cell-specific Nrp1 deficiency (Nrp1ΔIEC) results in decreased Hh pathway activity and a weakened gut barrier. In addition, Nrp1ΔIEC mice have a reduced density of capillary networks in their small intestinal villus structures. Collectively, our results reveal a role for the commensal microbiota and epithelial NRP1 signaling in the regulation of intestinal barrier function through postnatal control of Hh signaling.show moreshow less

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Metadaten
Author:Giulia PontarolloORCiD, Bettina Kollar, Amrit Mann, My Phung KhuuORCiD, Klytaimnistra KiouptsiORCiD, Franziska Bayer, Inês BrandãoORCiD, Valeriya V. ZininaORCiD, Jennifer Hahlbrock, Frano Malinarich, Maximilian MimmlerORCiD, Sudhanshu Bhushan, Federico Marini, Wolfram RufORCiD, Meriem BelheouaneORCiD, John F. Baines, Kristina EndresORCiD, Scott M. Reba, Verena K. RakerORCiDGND, Carsten DeppermannORCiD, Christoph WelschORCiD, Markus BosmannORCiD, Natalia SoshnikovaORCiD, Benoit Chassaing, Mattias Bergentall, Felix SommerORCiD, Fredrik Bäckhed, Christoph ReinhardtORCiD
URN:urn:nbn:de:bvb:384-opus4-1187570
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/118757
ISSN:2522-5812OPAC
Parent Title (English):Nature Metabolism
Publisher:Springer Science and Business Media LLC
Type:Article
Language:English
Year of first Publication:2023
Publishing Institution:Universität Augsburg
Release Date:2025/02/01
Volume:5
Issue:7
First Page:1174
Last Page:1187
Note:
Author correction published at: https://doi.org/10.1038/s42255-023-00901-z
DOI:https://doi.org/10.1038/s42255-023-00828-5
Institutes:Medizinische Fakultät
Medizinische Fakultät / Universitätsklinikum
Medizinische Fakultät / Professur für Experimentelle Allergologie und immunologische Intoleranz
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Licence (German):CC-BY 4.0: Creative Commons: Namensnennung (mit Print on Demand)