Gut microbiota-derived propionate regulates the expression of Reg3 mucosal lectins and ameliorates experimental colitis in mice Journal Article


Authors: Bajic, D.; Niemann, A.; Hillmer, A. K.; Mejias-Luque, R.; Bluemel, S.; Docampo, M.; Funk, M. C.; Tonin, E.; Boutros, M.; Schnabl, B.; Busch, D. H.; Miki, T.; Schmid, R. M.; van den Brink, M. R. M.; Gerhard, M.; Stein-Thoeringer, C. K.
Article Title: Gut microbiota-derived propionate regulates the expression of Reg3 mucosal lectins and ameliorates experimental colitis in mice
Abstract: Background and Aims: Regenerating islet-derived protein type 3 [Reg3] lectins are antimicrobial peptides at mucosal surfaces of the gut, whose expression is regulated by pathogenic gut microbes via interleukin-22- or Toll-like receptor signalling. In addition to antimicrobial effects, tissue protection is hypothesized, but has been poorly investigated in the gut. Methods: We applied antibiotic-induced microbiota perturbations, gnotobiotic approaches and a dextran-sodium sulfate [DSS] colitis model to assess microbial Reg3 regulation in the intestines and its role in colitis. We also used an intestinal organoid model to investigate this axis in vitro. Results: First, we studied whether gut commensals are involved in Reg3 expression in mice, and found that antibiotic-mediated reduction of Clostridia downregulated intestinal Reg3B. A loss in Clostridia was accompanied by a significant reduction of short-chain fatty acids [SCFAs], and knock-out [KO] mice for SCFA receptors GPR43 and GPR109 expressed less intestinal Reg3B/-G. Propionate was found to induce Reg3 in intestinal organoids and in gnotobiotic mice colonized with a defined, SCFA-producing microbiota. Investigating the role of Reg3B as a protective factor in colitis, we found that Reg3B-KO mice display increased inflammation and less crypt proliferation in the DSS colitis model. Propionate decreased colitis and increased proliferation. Treatment of organoids exposed to DSS with Reg3B or propionate reversed the chemical injury with a loss of expression of the stem-cell marker Lgr5 and Olfm4. Conclusions: Our results suggest that Clostridia can regulate Reg3-associated epithelial homeostasis through propionate signalling. We also provide evidence that the Reg3-propionate axis may be an important mediator of gut epithelial regeneration in colitis.
Keywords: inflammation; colitis; host; stem-cells; responses; mechanisms; potential; rifaximin; intestinal microbiota; microbiome; article; chain fatty-acids; alters; reg3; propionate
Journal Title: Journal of Crohns & Colitis
Volume: 14
Issue: 10
ISSN: 1873-9946
Publisher: Oxford University Press  
Date Published: 2020-10-01
Start Page: 1462
End Page: 1472
Language: English
ACCESSION: WOS:000593067100014
DOI: 10.1093/ecco-jcc/jjaa065
PROVIDER: wos
PUBMED: 32227170
PMCID: PMC8921751
Notes: Article -- Source: Wos
Altmetric
Citation Impact
MSK Authors
  1. Melissa   Docampo
    23 Docampo