Mechanisms and Therapeutic Implications of the Pregnane X Receptor Targeting Indole Bacterial Metabolites in Inflammatory Bowel Disease
Abstract
This proposal addresses a significant medical problem, namely, infection triggered inflammation in the intestines (technically called post-infectious inflammatory bowel disease) in military personnel. Compromised gut barrier integrity is an important risk factor that contributes to the onset of IBD, especially post-infection. The environmental cues and its molecular controls regulating intestinal barrier function are poorly understood in homeostatic and pathophysiologic states like infection-induced IBD. Our studies show a novel direct link between intestinal microbial metabolism (i.e. specific microbial metabolites) and regulation of intestinal permeability via a pathway regulated by an orphan nuclear receptor, PXR, and TLR4. We demonstrate that in the small intestines(which mirrors what happens in large intestines), where PXR is expressed in intestinal epithelial cells in a crypt-villus gradient, in homeostasis, dietary tryptophan-derived bacterial metabolites (i.e. indoles and indole metabolites in particular indole 3 propionic acid or IPA) tonically activate PXR and induce a down-regulation of the Toll-like Receptors, in particular TLR4, and its downstream signaling pathway. This results in modulating the abundance of TNF-alpha, which in turn modulates intestinal barrier function (i.e. permeability). In the context of an inappropriate increase in inflammatory signals (e.g., infection), suppression of PXR, and/or excess loss of dietary modulators (e.g., tryptophan), and/or specific indole metabolizing bacteria (e.g., antibiotics) results in increased permeability, thus exacerbating underlying disease predisposition and pathology. In this model, restitution of signaling homeostasis, either by reconstituting.
Document Details
- Document Type
- Technical Report
- Publication Date
- Jan 01, 2021
- Accession Number
- AD1151174
Entities
People
- Kamal M. Khanna
Organizations
- New York University