INTESTINAL DISTRIBUTION OF HUMAN NA+ H+ EXCHANGER ISOFORMS NHE-1, NHE-2, AND NHE-3 MESSENGER-RNA/

Citation
Pk. Dudeja et al., INTESTINAL DISTRIBUTION OF HUMAN NA+ H+ EXCHANGER ISOFORMS NHE-1, NHE-2, AND NHE-3 MESSENGER-RNA/, American journal of physiology: Gastrointestinal and liver physiology, 34(3), 1996, pp. 483-493
Citations number
41
Categorie Soggetti
Physiology
ISSN journal
01931857
Volume
34
Issue
3
Year of publication
1996
Pages
483 - 493
Database
ISI
SICI code
0193-1857(1996)34:3<483:IDOHNH>2.0.ZU;2-#
Abstract
The identity of Na+/H+ exchanger (NHE) isoforms in the human small int estine and colon and their role in vectorial Na+ absorption are not kn own. The present studies were undertaken to examine the regional and v ertical axis distribution of NHE-1, NHE-2, and NHE-3 mRNA in the human intestine. Ribonuclease protection assays were used to quantitate the levels of mRNA of these isoforms in various regions of the human inte stine. In situ hybridization technique was used to localize NHE-2 and NHE-3 mRNA in the colon. The NHE-1 isoform message was present uniform ly throughout the length of the human intestine. In contrast, mRNA lev els for human NHE-2 and NHE-3 isoforms demonstrated significant region al differences. The NHE-3 abundance was found in decreasing order: ile um > jejunum > proximal colon = distal colon. The NHE-2 message level in the distal colon was significantly higher than in the proximal colo n but was evenly distributed in the small intestine. In addition, NHE- 2 mRNA was present in surface epithelial cells as well as in cells of the crypt region, suggesting the presence of NHE-2 message throughout the vertical axis of the colonic crypts. In contrast, NHE-3 mRNA was l ocalized to surface colonocytes in the proximal colon. On the basis of this tissue-specific localization of NHE-2 and NHE-3 mRNA, it can be speculated that the relative contribution of NHE-2 and NHE-3 isoforms in Na+ absorption in the human intestine may be region specific, and t hese putative apical isoforms may be differentially regulated.