Characterization of acid-base transporters in cultured outer medullary collecting duct cells

Am J Physiol. 1992 Dec;263(6 Pt 2):F996-1003. doi: 10.1152/ajprenal.1992.263.6.F996.

Abstract

Cells from the inner stripe of the rabbit outer medullary collecting duct (OMCDi) were grown in primary culture, and their acid-base transport properties were characterized using intracellular pH (pHi) measurements with the fluorescent probe 2',7'-bis(carboxyethyl)-5(6)-carboxyfluorescein (BCECF). Basal pHi in HCO(3-)-buffered solutions was 7.28 +/- 0.04 (n = 20). The presence of a Cl-/HCO(3-)-antiporter was demonstrated by reversible alkalinization on bath Cl- removal. The mean alkalinization seen on Cl- removal was 0.16 +/- 0.02 pH units (n = 20) and was inhibited 92% by 10(-4) M 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid. Studies were also performed to determine the presence of an Na+/H+ antiporter and an H(+)-adenosinetriphosphatase (H(+)-ATPase). After an NH4Cl acid load the cells exhibited both Na(+)-dependent and Na(+)-independent pHi recovery mechanisms. The Na(+)-dependent mechanism was inhibited by amiloride. The Na(+)-independent mechanism was completely inhibited by 10(-3) M N-ethylmaleimide or 2.5 x 10(-9) M bafilomycin A1, but was not significantly altered by removal of bathing solution K+. Thus, the Na(+)-dependent recovery mechanism exhibited characteristics of an Na+/H+ antiporter, whereas the Na(+)-independent recovery mechanism was consistent with the presence of an H(+)-ATPase.

Publication types

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

MeSH terms

  • Animals
  • Carrier Proteins / metabolism*
  • Cells, Cultured
  • Chloride-Bicarbonate Antiporters
  • Female
  • Fluoresceins
  • H(+)-K(+)-Exchanging ATPase / metabolism*
  • Kidney Medulla
  • Kidney Tubules, Collecting / cytology
  • Kidney Tubules, Collecting / metabolism*
  • Proton Pump Inhibitors
  • Rabbits
  • Sodium-Hydrogen Exchangers

Substances

  • Carrier Proteins
  • Chloride-Bicarbonate Antiporters
  • Fluoresceins
  • Proton Pump Inhibitors
  • Sodium-Hydrogen Exchangers
  • 2',7'-bis(carboxyethyl)-5(6)-carboxyfluorescein
  • H(+)-K(+)-Exchanging ATPase