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Dual regulation of the native ClC-K2 chloride channel in the distal nephron by voltage and pH

机译:电压和pH值双重调节远端肾单位中天然ClC-K2氯化物通道

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摘要

ClC-K2, a member of the ClC family of Cl channels and transporters, forms the major basolateral Cl conductance in distal nephron epithelial cells and therefore plays a central role in renal Cl absorption. However, its regulation remains largely unknown because of the fact that recombinant ClC-K2 has not yet been studied at the single-channel level. In the present study, we investigate the effects of voltage, pH, Cl, and Ca2+ on native ClC-K2 in the basolateral membrane of intercalated cells from the mouse connecting tubule. The ∼10-pS channel shows a steep voltage dependence such that channel activity increases with membrane depolarization. Intracellular pH (pHi) and extracellular pH (pHo) differentially modulate the voltage dependence curve: alkaline pHi flattens the curve by causing an increase in activity at negative voltages, whereas alkaline pHo shifts the curve toward negative voltages. In addition, pHi, pHo, and extracellular Ca2+ strongly increase activity, mainly because of an increase in the number of active channels with a comparatively minor effect on channel open probability. Furthermore, voltage alters both the number of active channels and their open probability, whereas intracellular Cl has little influence. We propose that changes in the number of active channels correspond to them entering or leaving an inactivated state, whereas modulation of open probability corresponds to common gating by these channels. We suggest that pH, through the combined effects of pHi and pHo on ClC-K2, might be a key regulator of NaCl absorption and Cl/HCO3 exchange in type B intercalated cells.
机译:ClC-K2是Cl -通道和转运蛋白的ClC家族的成员,在远端肾单位上皮细胞中形成主要的基底外侧Cl -电导,因此在肾脏Cl -的吸收。然而,由于尚未在单通道水平上研究重组C1C-K2,因此其调节仍然很大程度上未知。在本研究中,我们研究了电压,pH,Cl -和Ca 2 + 对小鼠插层细胞基底外侧膜天然ClC-K2的影响连接小管。 〜10 pS通道显示出陡峭的电压依赖性,因此通道活性随膜去极化而增加。细胞内pH(pHi)和细胞外pH(pHo)不同地调节电压依赖性曲线:碱性pHi通过引起负电压下的活性增加而使曲线变平,而碱性pHo使曲线向负电压移动。此外,pHi,pHo和细胞外Ca 2 + 大大增强了活性,这主要是由于有效通道数量的增加,而对通道打开概率的影响相对较小。此外,电压会改变活动通道的数量及其开放概率,而细胞内Cl -的影响很小。我们提出,活动通道数的变化对应于它们进入或离开非激活状态,而打开概率的调制对应于这些通道的通用门控。我们建议通过pHi和pHo对ClC-K2的共同作用,pH可能是B型NaCl吸收和Cl - / HCO3 -交换的关键调节剂插入细胞。

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