In Vivo Evidence for Interferon-[gamma]-mediated Homeostatic Mechanisms in Small Intestine of the NHE3 Na super(+)/H super(+) Exchanger Knockout Model of Congenital Diarrhea

• Published in: The Journal of biological chemistry 2002-12, Vol.277 (50), p.49036-49046
• Main Authors: Woo, AL, Gildea, LA, Tack, L M, Miller, M L, Spicer, Z, Millhorn, DE, Finkelman, F D, Hassett, D J, Shull, GE
• Format: Article
• Language: English
• ISSN: 0021-9258

Mice lacking NHE3, the major absorptive Na super(+)/H super(+) exchanger in the intestine, are the only animal model of congenital diarrhea. To identify molecular changes underlying compensatory mechanisms activated in chronic diarrheas, cDNA microarrays and Northern blot analyses were used to compare global mRNA expression patterns in small intestine of NHE3-deficient and wild-type mice. Among the genes identified were members of the RegIII family of growth factors, which may contribute to the increased absorptive area, and a large number of interferon-[gamma]-responsive genes. The latter finding is of particular interest, since interferon-[gamma] has been shown to regulate ion transporter activities in intestinal epithelial cells. Serum interferon-[gamma] was elevated 5-fold in NHE3-deficient mice; however, there was no evidence of inflammation, and unlike conditions such as inflammatory bowel disease, levels of other cytokines were unchanged. In addition, quantitative PCR analysis showed that up-regulation of interferon-[gamma] mRNA was localized to the small intestine and did not occur in the colon, spleen, or kidney. These in vivo data suggest that elevated interferon-[gamma], produced by gut-associated lymphoid tissue in the small intestine, is part of a homeostatic mechanism that is activated in response to the intestinal absorptive defect in order to regulate the fluidity of the intestinal tract.