首页> 外文OA文献 >Caractérisation des canaux potassiques du tubule contourné proximal et des propriétés régulatrices des canaux chlorure de la membrane basolatérale des cellules intercalaires du tubule connecteur
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Caractérisation des canaux potassiques du tubule contourné proximal et des propriétés régulatrices des canaux chlorure de la membrane basolatérale des cellules intercalaires du tubule connecteur

机译:近曲小管的钾通道的特征以及连接器小管的互连细胞的基底外侧膜的氯化物通道的调节特性

摘要

A 10 pS chloride channel at the basolateral side of connecting duct intercalated cells shares properties with the cloned ClC-K2 channel. Patch-clamp experiments show that its activity and the number of active channels increase with (i) membrane depolarization (ii) external calcium concentration and (iii) external and internal alkalinization. External alkalinization also shifts the voltage-dependence curve towards negative voltages while internal alkalinization flattens the voltage-dependence curve thereby raising channel activity at negative potentials. These data suggest that extracellular calcium and both extra and intracellular protons modulate ClC-K2 channels activity through an action on the common gate rather than on the protopores present in others ClC channels.The role and the molecular identity of basolateral potassium channels of the proximal convoluted tubule (PCT) are not very well known. RT-PCR results revealed the presence of mRNA encoding the Kir4.2 and Kir5.1 potassium channels subunits in mouse PCT tubular cells, and western blot and immunohistochemistry experiments showed that both proteins are expressed at the basolateral membrane of these cells. The most frequent channel observed by patch-clamp on the basolateral membrane of PCT presents a conductance of 47 pS, an inward rectification induced by intracellular Mg2+, an inhibition by extracellular Ba2+ and an activity dependent on intracellular pH. These electrophysiological properties are consistent with the presence of heteromeric Kir4.2/Kir5.1 channels in the basolateral membrane of mouse PCT. The study of mice knocked out for the Kir4.2-encoding gene Kcnj15 did not highlight a renal phenotype.
机译:连接导管插入细胞的基底外侧的10 pS氯离子通道与克隆的ClC-K2通道共享特性。膜片钳实验表明,其活性和有效通道数随(i)膜去极化(ii)外部钙浓度和(iii)外部和内部碱化而增加。外部碱化还将电压依赖性曲线移向负电压,而内部碱化使电压依赖性曲线变平,从而提高了负电位下的通道活性。这些数据表明细胞外钙以及细胞外和细胞内质子均通过作用于共同门而不是其他ClC通道中存在的原孔的作用来调节ClC-K2通道的活性。近端旋旋的基底外侧钾通道的作用和分子身份输卵管(PCT)不是很了解。 RT-PCR结果显示在小鼠PCT肾小管细胞中存在编码Kir4.2和Kir5.1钾通道亚基的mRNA,western印迹和免疫组织化学实验表明这两种蛋白均在这些细胞的基底外侧膜上表达。通过膜片钳在PCT的基底外侧膜上观察到的最频繁的通道呈现出47 pS的电导率,由细胞内Mg2 +诱导的向内整流,细胞外Ba2 +的抑制作用以及取决于细胞内pH的活性。这些电生理特性与小鼠PCT基底外侧膜中存在异源Kir4.2 / Kir5.1通道一致。对敲除Kir4.2编码基因Kcnj15的小鼠的研究未突出显示肾脏表型。

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    Pinelli Laurent;

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  • 年度 2015
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