DMBT1 Confers Mucosal Protection In Vivo and a Deletion Variant Is Associated With Crohn's Disease

Marcus Renner, Gaby Bergmann, Inge Krebs, Caroline End, Stefan Lyer, Frank Hilberg, Burkhard Helmke, Nikolaus Gassler, Frank Autschbach, Floris Bikker, Olga Strobel-Freidekind, Sabine Gronert-Sum, Axel Benner, Stephanie Blaich, Rainer Wittig, Melanie Hudler, Antoon J. Ligtenberg, Jens Madsen, Uffe Holmskov, Vito AnneseAnna Latiano, Peter Schirmacher, Arie V Nieuw Amerongen, Mauro D'Amato, Petra Kioschis, Mathias Hafner, Annemarie Poustka, Jan Mollenhauer

Research output: Contribution to journalArticle

Abstract

Background & Aims: Impaired mucosal defense plays an important role in the pathogenesis of Crohn's disease (CD), one of the main subtypes of inflammatory bowel disease (IBD). Deleted in malignant brain tumors 1 (DMBT1) is a secreted scavenger receptor cysteine-rich protein with predominant expression in the intestine and has been proposed to exert possible functions in regenerative processes and pathogen defense. Here, we aimed at analyzing the role of DMBT1 in IBD. Methods: We studied DMBT1 expression in IBD and normal tissues by quantitative reverse transcription-polymerase chain reaction, immunohistochemistry, and mRNA in situ hybridization. Genetic polymorphisms within DMBT1 were analyzed in an Italian IBD case-control sample. Dmbt1-/- mice were generated, characterized, and analyzed for their susceptibility to dextran sulfate sodium-induced colitis. Results: DMBT1 levels correlate with disease activity in inflamed IBD tissues. A highly significant fraction of the patients with IBD displayed up-regulation of DMBT1 specifically in the intestinal epithelial surface cells and Paneth cells. A deletion allele of DMBT1 with a reduced number of scavenger receptor cysteine-rich domain coding exons is associated with an increased risk of CD (P = .00056; odds ratio, 1.75) but not for ulcerative colitis. Dmbt1-/- mice display enhanced susceptibility to dextran sulfate sodium-induced colitis and elevated Tnf, Il6, and Nod2 expression levels during inflammation. Conclusions: DMBT1 may play a role in intestinal mucosal protection and prevention of inflammation. Impaired DMBT1 function may contribute to the pathogenesis of CD.

Original languageEnglish
Pages (from-to)1499-1509
Number of pages11
JournalGastroenterology
Volume133
Issue number5
DOIs
Publication statusPublished - Nov 2007

ASJC Scopus subject areas

  • Gastroenterology

Fingerprint Dive into the research topics of 'DMBT1 Confers Mucosal Protection In Vivo and a Deletion Variant Is Associated With Crohn's Disease'. Together they form a unique fingerprint.

  • Cite this

    Renner, M., Bergmann, G., Krebs, I., End, C., Lyer, S., Hilberg, F., Helmke, B., Gassler, N., Autschbach, F., Bikker, F., Strobel-Freidekind, O., Gronert-Sum, S., Benner, A., Blaich, S., Wittig, R., Hudler, M., Ligtenberg, A. J., Madsen, J., Holmskov, U., ... Mollenhauer, J. (2007). DMBT1 Confers Mucosal Protection In Vivo and a Deletion Variant Is Associated With Crohn's Disease. Gastroenterology, 133(5), 1499-1509. https://doi.org/10.1053/j.gastro.2007.08.007