Native and recombinant Slc26a3 (downregulated in adenoma, Dra) do not exhibit properties of 2Cl-/1HCO3- exchange

被引:28
作者
Alper, Seth L. [3 ,4 ,5 ]
Stewart, Andrew K. [3 ,4 ,5 ]
Vandorpe, David H. [3 ,4 ,5 ]
Clark, Jeffrey S. [3 ,4 ,5 ]
Horack, R. Zachary [2 ]
Simpson, Janet E. [2 ]
Walker, Nancy M. [2 ]
Clarke, Lane L. [1 ,2 ]
机构
[1] Univ Missouri, Dalton Cardiovasc Res Ctr 324 D, Dept Biomed Sci, Columbia, MO 65211 USA
[2] Univ Missouri, Dalton Cardiovasc Res Ctr, Columbia, MO 65211 USA
[3] Beth Israel Deaconess Med Ctr, Div Renal, Boston, MA 02215 USA
[4] Beth Israel Deaconess Med Ctr, Div Mol & Vasc Med, Boston, MA 02215 USA
[5] Harvard Univ, Sch Med, Dept Med, Boston, MA 02215 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2011年 / 300卷 / 02期
基金
美国国家卫生研究院;
关键词
anion exchange; bicarbonate secretion; cystic fibrosis transmembrane conductance regulator; mouse; NaCl absorption; CONGENITAL CHLORIDE DIARRHEA; NH2-TERMINAL CYTOPLASMIC DOMAIN; INTESTINAL CL-/HCO3-EXCHANGER; RABBIT DISTAL COLON; ANION-EXCHANGER; INTRACELLULAR PH; CYSTIC-FIBROSIS; VILLOUS EPITHELIUM; CAMP INHIBITION; XENOPUS OOCYTES;
D O I
10.1152/ajpcell.00366.2010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Alper SL, Stewart AK, Vandorpe DH, Clark JS, Horack RZ, Simpson JE, Walker NM, Clarke LL. Native and recombinant Slc26a3 (downregulated in adenoma, Dra) do not exhibit properties of 2Cl(-)/1HCO(3)(-) exchange. Am J Physiol Cell Physiol 300: C276-C286, 2011. First published November 10, 2010; doi: 10.1152/ajpcell.00366.2010.-The recent proposal that Dra/Slc26a3 mediates electrogenic 2Cl(-)/1HCO(3)(-) exchange suggests a required revision of classical concepts of electroneutral Cl- transport across epithelia such as the intestine. We investigated 1) the effect of endogenous Dra Cl-/HCO3- activity on apical membrane potential (V-a) of the cecal surface epithelium using wild-type (WT) and knockout (KO) mice; and 2) the electrical properties of Cl-/(OH-) HCO3- exchange by mouse and human orthologs of Dra expressed in Xenopus oocytes. Ex vivo Cl-36(-) fluxes and microfluorometry revealed that cecal Cl-/HCO3- exchange was abolished in the Dra KO without concordant changes in short-circuit current. In microelectrode studies, baseline V-a of Dra KO surface epithelium was slightly hyperpolarized relative to WT but depolarized to the same extent as WT during luminal Cl- substitution. Subsequent studies indicated that Cl--dependent V-a depolarization requires the anion channel Cftr. Oocyte studies demonstrated that Dra-mediated exchange of intracellular Cl- for extracellular HCO3- is accompanied by slow hyperpolarization and a modest outward current, but that the steady-state current-voltage relationship is unaffected by Cl- removal or pharmacological blockade. Further, Dra-dependent Cl-36(-) efflux was voltage-insensitive in oocytes coexpressing the cation channels ENaC or ROMK. We conclude that 1) endogenous Dra and recombinant human/mouse Dra orthologs do not exhibit electrogenic 2Cl(-)/1HCO(3)(-) exchange; and 2) acute induction of Dra Cl-/HCO3- exchange is associated with secondary membrane potential changes representing homeostatic responses. Thus, participation of Dra in coupled NaCl absorption and in uncoupled HCO3- secretion remains compatible with electroneutrality of these processes, and with the utility of electroneutral transport models for predicting epithelial responses in health and disease.
引用
收藏
页码:C276 / C286
页数:11
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