Dietary AhR Ligands Regulate AhRR Expression in Intestinal Immune Cells and Intestinal Microbiota Composition

Int J Mol Sci. 2020 Apr 30;21(9):3189. doi: 10.3390/ijms21093189.

Abstract

A diet rich in vegetables and fruit is generally considered healthy because of a high content of phytochemicals, vitamins, and fiber. The phytochemical indole-3-carbinol (I3C), a derivative of glucobrassicin, is sold as a dietary supplement promising diverse health benefits. I3C metabolites act as ligands of the aryl hydrocarbon receptor (AhR), an important sensor for environmental polyaromatic chemicals. Here, we investigated how dietary AhR ligand supplementation influences AhR target gene expression and intestinal microbiota composition. For this, we used AhR repressor (AhRR)-reporter mice as a tool to study AhR activation in the intestine following dietary I3C-supplementation in comparison with AhR ligand-deprived diets, including a high fat diet. AhRR expression in intestinal immune cells was mainly driven by dietary AhR ligands and was independent of microbial metabolites. A lack of dietary AhR ligands caused enhanced susceptibility to dextran sodium sulfate (DSS)-induced colitis and correlated with the expansion of Enterobacteriaceae, whereas Clostridiales, Muribaculaceae, and Rikenellaceae were strongly reduced. I3C supplementation largely reverted this effect. Comparison of I3C-induced changes in microbiota composition using wild-type (WT), AhRR-deficient, and AhR-deficient mice revealed both AhR-dependent and -independent alterations in the microbiome. Overall, our study demonstrates that dietary AhR ligand supplementation has a profound influence on Ahrr expression in intestinal immune cells as well as microbiota composition.

Keywords: mucosal immunity, colitis, microbiome, aryl hydrocarbon receptor, aryl hydrocarbon receptor repressor, phytochemicals.

MeSH terms

  • Animals
  • Colitis / chemically induced
  • Colitis / drug therapy
  • Colitis / metabolism
  • Dextran Sulfate / toxicity
  • Female
  • Flow Cytometry
  • Gastrointestinal Microbiome / drug effects*
  • Indoles / pharmacology*
  • Indoles / therapeutic use
  • Male
  • Mice
  • RNA, Ribosomal, 16S / genetics
  • RNA, Ribosomal, 16S / metabolism
  • Real-Time Polymerase Chain Reaction
  • Receptors, Aryl Hydrocarbon / genetics
  • Receptors, Aryl Hydrocarbon / metabolism*

Substances

  • Indoles
  • RNA, Ribosomal, 16S
  • Receptors, Aryl Hydrocarbon
  • Dextran Sulfate
  • indole-3-carbinol