Deficient acid handling with distal RTA in the NBCe2 knockout mouse

Am J Physiol Renal Physiol. 2015 Sep 15;309(6):F523-30. doi: 10.1152/ajprenal.00163.2015. Epub 2015 Jun 24.

Abstract

In many circumstances, the pathogenesis of distal renal tubular acidosis (dRTA) is not understood. In the present study, we report that a mouse model lacking the electrogenic Na(+)-HCO3 (-) cotransporter [NBCe2/Slc4a5; NBCe2 knockout (KO) mice] developed dRTA after an oral acid challenge. NBCe2 expression was identified in the connecting tubule (CNT) of wild-type mice, and its expression was significantly increased after acid loading. NBCe2 KO mice did not have dRTA when on a standard mouse diet. However, after acid loading, NBCe2 KO mice exhibited complete features of dRTA, characterized by insufficient urinary acidification, hyperchloremic hypokalemic metabolic acidosis, and hypercalciuria. Additional experiments showed that NBCe2 KO mice had decreased luminal transepithelial potential in the CNT, as revealed by micropuncture. Further immunofluorescence and Western blot experiments found that NBCe2 KO mice had increased expression of H(+)-ATPase B1 in the plasma membrane. These results showed that NBCe2 KO mice with acid loading developed increased urinary K(+) and Ca(2+) wasting due to decreased luminal transepithelial potential in the CNT. NBCe2 KO mice compensated to maintain systemic pH by increasing H(+)-ATPase in the plasma membrane. Therefore, defects in NBCe2 can cause dRTA, and NBCe2 has an important role to regulate urinary acidification and the transport of K(+) and Ca(2+) in the distal nephron.

Keywords: connecting tubule; distal renal tubular acidosis; electrogenic Na+-HCO3− cotransporter.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acidosis, Renal Tubular / metabolism*
  • Animals
  • Cell Membrane / metabolism
  • Chlorine / metabolism
  • Hypercalciuria / metabolism
  • Hypokalemia / metabolism
  • Kidney Tubules, Distal / metabolism*
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Proton-Translocating ATPases / metabolism
  • Sodium-Bicarbonate Symporters / genetics*
  • Sodium-Bicarbonate Symporters / metabolism
  • Sodium-Bicarbonate Symporters / physiology*

Substances

  • Membrane Proteins
  • SLC4A5 protein, mouse
  • Sodium-Bicarbonate Symporters
  • Chlorine
  • Proton-Translocating ATPases