Enteric nematodes induce stereotypic STAT6-dependent alterations in intestinal epithelial cell function

J Immunol. 2004 May 1;172(9):5616-21. doi: 10.4049/jimmunol.172.9.5616.

Abstract

Infection with gastrointestinal nematodes exerts profound effects on both the immune and physiological responses of the host. We showed previously that the Th2 cytokines, IL-4 and IL-13, induce STAT6-dependent changes in intestinal epithelial cell permeability, absorption, and secretion that are similar to those observed in a secondary infection with Heligmosomoides polygyrus. In the current study we investigated whether nematode-induced effects on epithelial cell function were 1) generic, 2) dependent upon STAT6, and 3) attributable to direct effects on the epithelial cells themselves or mediated by effects on enteric nerves. Our results demonstrate that infection of BALB/c mice with three different gastrointestinal nematodes (H. polygyrus, Nippostrongylus brasiliensis, and Trichinella spiralis) alters intestinal epithelial cell function by decreasing resistance, glucose absorption, and secretory responses to 5-hydroxytryptamine and acetylcholine, two critical mediators in the submucosal reflex pathway. These modified responses are dependent on STAT6 and are the result of both direct effects and indirect effects mediated through enteric nerves.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Membrane Permeability / physiology*
  • Female
  • Glucose / antagonists & inhibitors
  • Glucose / metabolism
  • Intestinal Absorption / genetics
  • Intestinal Absorption / immunology
  • Intestinal Diseases, Parasitic / immunology
  • Intestinal Diseases, Parasitic / pathology*
  • Intestinal Diseases, Parasitic / physiopathology*
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / innervation
  • Intestinal Mucosa / metabolism*
  • Intestinal Mucosa / pathology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Nematode Infections / immunology
  • Nematode Infections / pathology*
  • Nematode Infections / physiopathology*
  • Nematospiroides dubius / immunology
  • Nippostrongylus / immunology
  • STAT6 Transcription Factor
  • Sodium / metabolism
  • Tetrodotoxin / pharmacology
  • Trans-Activators / deficiency
  • Trans-Activators / genetics
  • Trans-Activators / physiology*
  • Trichinella spiralis / immunology

Substances

  • STAT6 Transcription Factor
  • Stat6 protein, mouse
  • Trans-Activators
  • Tetrodotoxin
  • Sodium
  • Glucose