Regulation of the T helper cell type 1 transcription factor T-bet in coeliac disease mucosa

Gut. 2004 Aug;53(8):1090-5. doi: 10.1136/gut.2003.030551.

Abstract

Background: In coeliac disease (CD) mucosa, the histological lesion is associated with marked infiltration of T helper cell type 1 (Th1) cells. However, the molecular mechanisms which regulate Th1 cell differentiation in CD mucosa are unknown.

Aims: To analyse expression of transcription factors which control the Th1 cell commitment in CD.

Patients: Duodenal mucosal samples were taken from untreated CD patients and normal controls.

Methods: Interferon gamma (IFN-gamma) and interleukin (IL)-4 RNA expression was examined in T lamina propria lymphocytes by quantitative reverse transcription-polymerase chain reaction. T-bet and STAT-4, two Th1 promoting transcription factors, and STAT-6 and GATA-3, transcription factors which govern T helper cell type 2 (Th2) cell polarisation, were examined in duodenal biopsies by western blotting. The effect of gliadin and IFN-gamma on expression of T-bet was examined in an ex vivo culture of biopsies taken from normal and treated CD patients.

Results: As expected, IFN-gamma but not IL-4 RNA transcripts were increased in the mucosa of CD patients in comparison with controls. CD mucosal samples consistently exhibited higher levels of T-bet than controls. However, no difference in active STAT-4 expression was seen between CD patients and controls, suggesting that Th1 polarisation was not induced by local IL-12. GATA-3 and STAT-6 were also low in both CD and control mucosa. In normal duodenal biopsies, IFN-gamma stimulated T-bet through a STAT-1 dependent mechanism. Challenge of treated CD but not control biopsies with gliadin enhanced T-bet and this effect was also inhibited by STAT-1 inhibition.

Conclusions: This study shows that activation of STAT-1 by IFN-gamma promotes T-bet in CD mucosa.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Celiac Disease / metabolism*
  • DNA-Binding Proteins / metabolism
  • Duodenum / metabolism
  • GATA6 Transcription Factor
  • Gliadin / genetics
  • Humans
  • Interferon-gamma / analysis
  • Interferon-gamma / genetics
  • Interleukin-4 / metabolism
  • Intestinal Mucosa / metabolism
  • Middle Aged
  • RNA / analysis
  • STAT1 Transcription Factor
  • STAT4 Transcription Factor
  • STAT6 Transcription Factor
  • Signal Transduction
  • T-Box Domain Proteins
  • Th1 Cells / physiology*
  • Trans-Activators / metabolism
  • Transcription Factors / metabolism*
  • Transcription, Genetic / genetics

Substances

  • DNA-Binding Proteins
  • GATA6 Transcription Factor
  • GATA6 protein, human
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • STAT4 Transcription Factor
  • STAT4 protein, human
  • STAT6 Transcription Factor
  • STAT6 protein, human
  • T-Box Domain Proteins
  • T-box transcription factor TBX21
  • Trans-Activators
  • Transcription Factors
  • Interleukin-4
  • RNA
  • Interferon-gamma
  • Gliadin