Differential expression of claudin-2 along the human intestine: Implication of GATA-4 in the maintenance of claudin-2 in differentiating cells

J Cell Physiol. 2005 Apr;203(1):15-26. doi: 10.1002/jcp.20189.

Abstract

Claudins, and particularly claudin-2, are important regulatory components of tight junction permeability. A better understanding of the involvement of claudin-2 in intestinal barrier functions requires the characterization of its distribution and regulation in the intestine. Interestingly, the claudin-2 gene promoter harbors a number of similarities to that of sucrase-isomaltase, a marker of enterocyte differentiation. We thus investigated the expression of claudin-2 in relation to the transcription factors CDX2, HNF-1alpha, and GATA-4 in the human intestine. The characterization of claudin-2 and the expression of the above transcription factors were performed by immunofluorescence, Western blot, and RT-PCR in the developing human intestinal epithelium. The functional role of CDX2, HNF-1alpha, and GATA-4 on claudin-2 regulation was also examined by ectopic expression studies in intestinal cell models. Claudin-2 was detected in both crypt and villus cells of the small intestine but restricted to undifferentiated crypt cells in the colon. CDX2 and HNF-1alpha were expressed along the entire intestine whereas GATA-4 was undetectable in the colon. Accordingly, in the colonic Caco-2 cell model, claudin-2 was found to be present only in undifferentiated cells. Like in the colonic epithelium, GATA-4 was found to be also lacking in Caco-2 cells while CDX2 and HNF-1alpha were present at significant levels. Cotransfection experiments showed that the claudin-2 promoter was activated by CDX2, HNF-1alpha, and GATA-4 in a cooperative manner. Furthermore, forced GATA-4 expression in Caco-2 cells enhances maintenance of claudin-2 expression during differentiation. These observations suggest that optimal claudin-2 expression in the gut relies on the presence of GATA-4, suggesting a role for this factor in intestinal regionalization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CDX2 Transcription Factor
  • Caco-2 Cells
  • Cell Differentiation / physiology
  • Claudins
  • Colon / cytology
  • Colon / physiology
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • GATA4 Transcription Factor
  • Gene Expression Regulation / physiology
  • Hepatocyte Nuclear Factor 1
  • Hepatocyte Nuclear Factor 1-alpha
  • Homeodomain Proteins / metabolism
  • Humans
  • Intestinal Mucosa / cytology*
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / physiology*
  • Intestine, Small / cytology
  • Intestine, Small / physiology
  • Membrane Proteins / biosynthesis
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Nuclear Proteins / metabolism
  • Promoter Regions, Genetic / physiology
  • Tight Junctions / physiology
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism

Substances

  • CDX2 Transcription Factor
  • CDX2 protein, human
  • CLDN2 protein, human
  • Claudins
  • DNA-Binding Proteins
  • GATA4 Transcription Factor
  • HNF1A protein, human
  • Hepatocyte Nuclear Factor 1-alpha
  • Homeodomain Proteins
  • Membrane Proteins
  • Nuclear Proteins
  • Transcription Factors
  • Hepatocyte Nuclear Factor 1