Glutamine supplementation attenuates expressions of adhesion molecules and chemokine receptors on T cells in a murine model of acute colitis

Mediators Inflamm. 2014:2014:837107. doi: 10.1155/2014/837107. Epub 2014 May 7.

Abstract

Background: Migration of T cells into the colon plays a major role in the pathogenesis in inflammatory bowel disease. This study investigated the effects of glutamine (Gln) supplementation on chemokine receptors and adhesion molecules expressed by T cells in mice with dextran sulfate sodium- (DSS-) induced colitis.

Methods: C57BL/6 mice were fed either a standard diet or a Gln diet replacing 25% of the total nitrogen. After being fed the diets for 5 days, half of the mice from both groups were given 1.5% DSS in drinking water to induce colitis. Mice were killed after 5 days of DSS exposure.

Results: DSS colitis resulted in higher expression levels of P-selectin glycoprotein ligand- (PSGL-) 1, leukocyte function-associated antigen- (LFA-) 1, and C-C chemokine receptor type 9 (CCR9) by T helper (Th) and cytotoxic T (Tc) cells, and mRNA levels of endothelial adhesion molecules in colons were upregulated. Gln supplementation decreased expressions of PSGL-1, LFA-1, and CCR9 by Th cells. Colonic gene expressions of endothelial adhesion molecules were also lower in Gln-colitis mice. Histological finding showed that colon infiltrating Th cells were less in the DSS group with Gln administration.

Conclusions: Gln supplementation may ameliorate the inflammation of colitis possibly via suppression of T cell migration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Administration, Oral
  • Animals
  • Body Weight
  • Cell Adhesion Molecules / metabolism*
  • Cell Movement
  • Colitis / metabolism*
  • Colitis / physiopathology
  • Colon / drug effects
  • Colon / pathology
  • Dietary Supplements*
  • Disease Models, Animal
  • Glutamine / therapeutic use*
  • Heparin / chemistry
  • Intestinal Mucosa / pathology
  • Leukocytes / drug effects
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microscopy, Fluorescence
  • Polysaccharides / chemistry
  • Receptors, CCR / metabolism
  • Receptors, Chemokine / metabolism*
  • T-Lymphocytes / cytology
  • T-Lymphocytes / metabolism*

Substances

  • CC chemokine receptor 9
  • Cell Adhesion Molecules
  • Polysaccharides
  • Receptors, CCR
  • Receptors, Chemokine
  • Glutamine
  • Heparin