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  3. Intelectin-1 binds and alters the localization of the mucus barrier-modifying bacterium Akkermansia muciniphila.
 

Intelectin-1 binds and alters the localization of the mucus barrier-modifying bacterium Akkermansia muciniphila.

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BORIS DOI
10.48350/191306
Date of Publication
January 2, 2023
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
Matute, Juan D
Duan, Jinzhi
Flak, Magdalena B
Griebel, Paul
Tascon-Arcila, Jose A
Doms, Shauni
Hanley, Thomas
Antanaviciute, Agne
Gundrum, Jennifer
Mark Welch, Jessica L
Sit, Brandon
Abtahi, Shabnam
Fuhler, Gwenny M
Grootjans, Joep
Tran, Florian
Stengel, Stephanie T
White, James R
Krupka, Niklasorcid-logo
Universitätsklinik für Viszerale Chirurgie und Medizin - Gastroenterologie
Haller, Dirk
Clare, Simon
Lawley, Trevor D
Kaser, Arthur
Simmons, Alison
Glickman, Jonathan N
Bry, Lynn
Rosenstiel, Philip
Borisy, Gary
Waldor, Matthew K
Baines, John F
Turner, Jerrold R
Blumberg, Richard S
Subject(s)

600 - Technology::610...

Series
The Journal of experimental medicine
ISSN or ISBN (if monograph)
1540-9538
Publisher
Rockefeller Univ. Press
Language
English
Publisher DOI
10.1084/jem.20211938
PubMed ID
36413219
Description
Intelectin-1 (ITLN1) is a lectin secreted by intestinal epithelial cells (IECs) and upregulated in human ulcerative colitis (UC). We investigated how ITLN1 production is regulated in IECs and the biological effects of ITLN1 at the host-microbiota interface using mouse models. Our data show that ITLN1 upregulation in IECs from UC patients is a consequence of activating the unfolded protein response. Analysis of microbes coated by ITLN1 in vivo revealed a restricted subset of microorganisms, including the mucolytic bacterium Akkermansia muciniphila. Mice overexpressing intestinal ITLN1 exhibited decreased inner colonic mucus layer thickness and closer apposition of A. muciniphila to the epithelial cell surface, similar to alterations reported in UC. The changes in the inner mucus layer were microbiota and A. muciniphila dependent and associated with enhanced sensitivity to chemically induced and T cell-mediated colitis. We conclude that by determining the localization of a select group of bacteria to the mucus layer, ITLN1 modifies this critical barrier. Together, these findings may explain the impact of ITLN1 dysregulation on UC pathogenesis.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/173132
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JEM_20211938.pdftextAdobe PDF6.41 MBpublishedOpen
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