Commensal bacteria-dependent indole production enhances epithelial barrier function in the colon

PLoS One. 2013 Nov 20;8(11):e80604. doi: 10.1371/journal.pone.0080604. eCollection 2013.

Abstract

Microbiota have been shown to have a great influence on functions of intestinal epithelial cells (ECs). The role of indole as a quorum-sensing (QS) molecule mediating intercellular signals in bacteria has been well appreciated. However, it remains unknown whether indole has beneficial effects on maintaining intestinal barriers in vivo. In this study, we analyzed the effect of indole on ECs using a germ free (GF) mouse model. GF mice showed decreased expression of junctional complex molecules in colonic ECs. The feces of specific pathogen-free (SPF) mice contained a high amount of indole; however the amount was significantly decreased in the feces of GF mice by 27-fold. Oral administration of indole-containing capsules resulted in increased expression of both tight junction (TJ)- and adherens junction (AJ)-associated molecules in colonic ECs in GF mice. In accordance with the increased expression of these junctional complex molecules, GF mice given indole-containing capsules showed higher resistance to dextran sodium sulfate (DSS)-induced colitis. A similar protective effect of indole on DSS-induced epithelial damage was also observed in mice bred in SPF conditions. These findings highlight the beneficial role of indole in establishing an epithelial barrier in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacteria / isolation & purification
  • Bacteria / metabolism*
  • Chromatography, High Pressure Liquid
  • Colon / metabolism
  • Colon / microbiology
  • Colon / physiology*
  • Germ-Free Life
  • Indoles / metabolism*
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / microbiology
  • Intestinal Mucosa / physiology*
  • Mice
  • Real-Time Polymerase Chain Reaction
  • Tandem Mass Spectrometry

Substances

  • Indoles

Grants and funding

This work was supported by a Grant-in-Aid from the Ministry of Education, Culture, Sports, Science and Technology (24390120); the Ministry of Health, Labour and Welfare; and the Osaka Foundation for the Promotion of Clinical Immunology. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.