Characterization of NA+/H+ exchanger isoform (NHE1, NH32 and NHE3) expression in prairie dog gallbladder

J Membr Biol. 2001 Jul 15;182(2):123-34. doi: 10.1007/s00232-001-0038-9.

Abstract

Gallbladder Na+ absorption is linked to gallstone formation in prairie dogs. Na+/H+ exchange (NHE) is one of the major Na+ absorptive pathways in gallbladder. In this study, we measured gallbladder Na+/H+ exchange and characterized the NHE isoforms expressed in prairie dogs. Na+/H+ exchange activity was assessed by measuring amiloride-inhibitable transepithelial Na+ flux and apical 22Na+ uptake using dimethylamiloride (DMA). HOE-694 was used to determine NHE2 and NHE3 contributions. Basal JNams was higher than JNasm with JNanet absorption. Mucosal DMA inhibited transepithelial Na+ flux in a dose-dependent fashion, causing JNams equal to JNasm and blocking JNanet absorption at 100 microm. Basal 22Na+ uptake rate was 10.9 +/- 1.0 micromol. cm-2. hr-1 which was inhibited by approximately 43% by mucosal DMA and approximately 30% by mucosal HOE-694 at 100 microm. RT-PCR and Northern blot analysis demonstrated expression of mRNAs encoding NHE1, NHE2 and NHE3 in the gallbladder. Expression of NHE1, NHE2 and NHE3 polypeptides was confirmed using isoform-specific anti-NHE antibodies. These data suggest that Na+/H+ exchange accounts for a substantial fraction of gallbladder apical Na+ entry and most of net Na+ absorption in prairie dogs. The NHE2 and NHE3 isoforms, but not NHE1, are involved in gallbladder apical Na+ uptake and transepithelial Na+ absorption.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amiloride / pharmacology
  • Animals
  • Biological Transport, Active
  • Blotting, Northern
  • Cholelithiasis / metabolism*
  • Disease Models, Animal
  • Electrophysiology
  • Epithelial Cells
  • Gallbladder / drug effects
  • Gallbladder / metabolism*
  • Guanidines / pharmacology
  • Immunoblotting
  • Male
  • Protein Isoforms / biosynthesis
  • Protein Isoforms / genetics
  • RNA / isolation & purification
  • Sciuridae
  • Sodium / metabolism*
  • Sodium-Hydrogen Exchanger 3
  • Sodium-Hydrogen Exchangers / biosynthesis*
  • Sodium-Hydrogen Exchangers / genetics
  • Sulfones / pharmacology

Substances

  • Guanidines
  • Protein Isoforms
  • Sodium-Hydrogen Exchanger 3
  • Sodium-Hydrogen Exchangers
  • Sulfones
  • growth factor-activatable Na-H exchanger NHE-1
  • 3-methylsulfonyl-4-piperidinobenzoyl guanidine
  • RNA
  • Amiloride
  • Sodium