Defective tight junctions in refractory celiac disease

Ann N Y Acad Sci. 2012 Jul:1258:43-51. doi: 10.1111/j.1749-6632.2012.06565.x.

Abstract

In celiac disease, the gut-associated immune system is activated in response to the ingestion of gluten, causing an atrophy of the small intestinal mucosa. Although this condition is, in most cases, responsive to a gluten-free diet, celiac disease refractory to treatment occurs in a small percentage of celiacs. An epithelial barrier defect is known to be an integral part of celiac pathophysiology. However, the mucosa in refractory celiac disease underlies a constant inflammatory process. The epithelial barrier has not been addressed in this condition so far. Herein, the tight junction-associated barrier in refractory celiac disease is investigated functionally and structurally. Although normally expressed in celiac disease, claudin-4 is shown to be downregulated in refractory cases, presumably by two mechanisms, reduced protein expression and increased claudin endocytosis. Furthermore, the tightening claudin-5 is downregulated and the pore-forming claudin-2 is upregulated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Blotting, Western
  • Caco-2 Cells
  • Case-Control Studies
  • Celiac Disease / immunology
  • Celiac Disease / physiopathology*
  • Claudins / metabolism
  • Dielectric Spectroscopy
  • Endocytosis
  • Female
  • Humans
  • Intestinal Mucosa / physiopathology
  • Male
  • Microscopy, Confocal
  • Middle Aged
  • Receptors, Antigen, T-Cell / immunology
  • Subcellular Fractions / metabolism
  • Tight Junctions / physiology*

Substances

  • Claudins
  • Receptors, Antigen, T-Cell