[go: up one dir, main page]

A Map of Toll-like Receptor Expression in the Intestinal Epithelium Reveals Distinct Spatial, Cell Type-Specific, and Temporal Patterns

Immunity. 2018 Sep 18;49(3):560-575.e6. doi: 10.1016/j.immuni.2018.07.016. Epub 2018 Aug 28.

Abstract

Signaling by Toll-like receptors (TLRs) on intestinal epithelial cells (IECs) is critical for intestinal homeostasis. To visualize epithelial expression of individual TLRs in vivo, we generated five strains of reporter mice. These mice revealed that TLR expression varied dramatically along the length of the intestine. Indeed, small intestine (SI) IECs expressed low levels of multiple TLRs that were highly expressed by colonic IECs. TLR5 expression was restricted to Paneth cells in the SI epithelium. Intestinal organoid experiments revealed that TLR signaling in Paneth cells or colonic IECs induced a core set of host defense genes, but this set did not include antimicrobial peptides, which instead were induced indirectly by inflammatory cytokines. This comprehensive blueprint of TLR expression and function in IECs reveals unexpected diversity in the responsiveness of IECs to microbial stimuli, and together with the associated reporter strains, provides a resource for further study of innate immunity.

Keywords: Paneth cells; TLR; innate immunity; intestinal epithelial cells; intestinal homeostasis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimicrobial Cationic Peptides / metabolism
  • Cells, Cultured
  • Colitis / chemically induced
  • Colitis / immunology*
  • Colon / pathology*
  • Cytokines / metabolism
  • Disease Models, Animal
  • Gene Expression Regulation
  • Homeostasis
  • Humans
  • Immunity, Innate
  • Inflammation Mediators / metabolism
  • Intestinal Mucosa / physiology*
  • Intestine, Small / pathology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Organ Specificity
  • Paneth Cells / physiology*
  • Receptor Cross-Talk
  • Signal Transduction
  • Toll-Like Receptor 5 / metabolism

Substances

  • Antimicrobial Cationic Peptides
  • Cytokines
  • Inflammation Mediators
  • Toll-Like Receptor 5