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Electrophysiological changes in Slc26a3 (down‐regulated in adenoma, Dra) knockout intestine are associated with epithelial cell alkalinity

Lane L. Clarke, R Horák, Janet E. Simpson, Nancy M. Walker

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Abstract

Dra is the major apical membrane anion exchanger in the small and large intestine. Studies of recombinant DRA have proposed an electrogenic 2Cl − :1HCO 3 − stoichiometry ( J. Gen. Physiol. 127: 511, 2006). However, in Dra knockout mice (DraKO) loss of Cl − absorption is associated with only small increases in transepithelial short‐circuit current (I sc ). To investigate the electrophysiological changes resulting from loss of Dra, microelectrode analysis, intracellular pH (pH i ) microfluorimetry and Ussing chamber studies were performed on DraKO and wild‐type (WT) intestine. Microelectrode studies revealed that the apical membrane potential (V a ) of cecal epithelium was paradoxically greater in the DraKO and V a depolarization induced by extracellular Cl − (Cl − o ) removal was not different than WT. Studies of cystic fibrosis mouse intestine indicated that V a depolarization during Cl − o removal was CFTR dependent and eliminated by high [K + ]. Microfluorimetry studies revealed alkaline pH i in DraKO small and large intestinal epithelia. Ussing chamber experiments of DraKO small intestine found that increased I sc was abolished by epithelial acidification. We conclude that intestinal Dra demonstrates an electroneutral stoichiometry (e.g., 1Cl − :1HCO 3 − ) and that increased I sc in DraKO intestine is associated with epithelial alkalinity that may activate basolateral membrane K + channels. Support: NIDDK and CFF.

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Dra is the major apical membrane anion exchanger in the small and large intestine. Studies of recombinant DRA have proposed an electrogenic 2Cl − :1HCO 3 − stoichiometry ( J. Gen. Physiol. 127: 511, 2006). However, in Dra knockout mice (DraKO) loss of Cl − absorption is associated with only small increases in transepithelial short‐circuit current (I sc ). To investigate the electrophysiological changes resulting from loss of Dra, microelectrode analysis, intracellular pH (pH i ) microfluorimetry and Ussing chamber studies were performed on DraKO and wild‐type (WT) intestine. Microelectrode studies revealed that the apical membrane potential (V a ) of cecal epithelium was paradoxically greater in the DraKO and V a depolarization induced by extracellular Cl − (Cl − o ) removal was not different than WT. Studies of cystic fibrosis mouse intestine indicated that V a depolarization during Cl − o removal was CFTR dependent and eliminated by high [K + ]. Microfluorimetry studies revealed alkaline pH i in DraKO small and large intestinal epithelia. Ussing chamber experiments of DraKO small intestine found that increased I sc was abolished by epithelial acidification. We conclude that intestinal Dra demonstrates an electroneutral stoichiometry (e.g., 1Cl − :1HCO 3 − ) and that increased I sc in DraKO intestine is associated with epithelial alkalinity that may activate basolateral membrane K + channels. Support: NIDDK and CFF.

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Available abstract

Dra is the major apical membrane anion exchanger in the small and large intestine. Studies of recombinant DRA have proposed an electrogenic 2Cl − :1HCO 3 − stoichiometry ( J. Gen. Physiol. 127: 511, 2006). However, in Dra knockout mice (DraKO) loss of Cl − absorption is associated with only small increases in transepithelial short‐circuit current (I sc ). To investigate the electrophysiological changes resulting from loss of Dra, microelectrode analysis, intracellular pH (pH i ) microfluorimetry and Ussing chamber studies were performed on DraKO and wild‐type (WT) intestine. Microelectrode studies revealed that the apical membrane potential (V a ) of cecal epithelium was paradoxically greater in the DraKO and V a depolarization induced by extracellular Cl − (Cl − o ) removal was not different than WT. Studies of cystic fibrosis mouse intestine indicated that V a depolarization during Cl − o removal was CFTR dependent and eliminated by high [K + ]. Microfluorimetry studies revealed alkaline pH i in DraKO small and large intestinal epithelia. Ussing chamber experiments of DraKO small intestine found that increased I sc was abolished by epithelial acidification. We conclude that intestinal Dra demonstrates an electroneutral stoichiometry (e.g., 1Cl − :1HCO 3 − ) and that increased I sc in DraKO intestine is associated with epithelial alkalinity that may activate basolateral membrane K + channels. Support: NIDDK and CFF.

Key concepts: Ussing chamber, Depolarization, Chemistry, Apical membrane, Transepithelial potential difference, Extracellular, Intracellular pH, Epithelial polarity

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