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
Abstract
Lane L. Clarke, R Horák, Janet E. Simpson, Nancy M. Walker
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.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
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