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天然和重组 Slc26a3(腺瘤下调,Dra)不表现出 2Cl-/1HCO3-交换的特性。

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

机构信息

Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Am J Physiol Cell Physiol. 2011 Feb;300(2):C276-86. doi: 10.1152/ajpcell.00366.2010. Epub 2010 Nov 10.

Abstract

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(-)/HCO(3)(-) 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(-))HCO(3)(-) exchange by mouse and human orthologs of Dra expressed in Xenopus oocytes. Ex vivo (36)Cl(-) fluxes and microfluorometry revealed that cecal Cl(-)/HCO(3)(-) 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 HCO(3)(-) 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 (36)Cl(-) 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(-)/HCO(3)(-) exchange is associated with secondary membrane potential changes representing homeostatic responses. Thus, participation of Dra in coupled NaCl absorption and in uncoupled HCO(3)(-) secretion remains compatible with electroneutrality of these processes, and with the utility of electroneutral transport models for predicting epithelial responses in health and disease.

摘要

最近有研究提出,Dra/Slc26a3 介导了电致 2Cl(-)/1HCO(3)(-)交换,这表明需要修正经典的上皮细胞跨膜电中性 Cl(-)转运概念,比如肠道。我们研究了 1)内源性 Dra Cl(-)/HCO(3)(-)活性对盲肠表面上皮顶端膜电位(V(a))的影响,方法是使用野生型(WT)和敲除(KO)小鼠;2)用表达在非洲爪蟾卵母细胞中的 Dra 及其鼠和人同源物来研究 Cl(-)/(OH(-))HCO(3)(-)交换的电学性质。离体(36)Cl(-)通量和微荧光法显示,在 Dra KO 中,肠 Cl(-)/HCO(3)(-)交换被消除,而短路电流没有相应改变。在微电极研究中,与 WT 相比,Dra KO 表面上皮的基线 V(a)略微超极化,但在腔内 Cl(-)替代时与 WT 一样去极化。进一步的研究表明,Cl(-)依赖性 V(a)去极化需要阴离子通道 Cftr。卵母细胞研究表明,Dra 介导的细胞内 Cl(-)与细胞外 HCO(3)(-)的交换伴随着缓慢的超极化和适度的外向电流,但稳态电流-电压关系不受 Cl(-)去除或药理学阻断的影响。此外,在共表达阳离子通道 ENaC 或 ROMK 的卵母细胞中,Dra 依赖性(36)Cl(-)外排对电压不敏感。我们的结论是 1)内源性 Dra 和重组人/鼠 Dra 同源物不表现出电致 2Cl(-)/1HCO(3)(-)交换;2)Dra Cl(-)/HCO(3)(-)交换的急性诱导与代表体内平衡反应的继发膜电位变化有关。因此,Dra 参与偶联的 NaCl 吸收和非偶联的 HCO(3)(-)分泌仍然与这些过程的电中性一致,并且电中性转运模型可用于预测健康和疾病状态下的上皮反应。

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