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肿胀激活的氯离子通道ClC-2、氯离子通道ClC-3以及在肾结石疾病中发生突变的氯离子通道ClC-5,在肾上皮细胞的不同亚群中表达。

The swelling-activated chloride channel ClC-2, the chloride channel ClC-3, and ClC-5, a chloride channel mutated in kidney stone disease, are expressed in distinct subpopulations of renal epithelial cells.

作者信息

Obermüller N, Gretz N, Kriz W, Reilly R F, Witzgall R

机构信息

Medical Research Center, Klinikum Mannheim, University of Heidelberg, D-68167 Mannheim, Germany.

出版信息

J Clin Invest. 1998 Feb 1;101(3):635-42. doi: 10.1172/JCI1496.

Abstract

The mammalian genome encodes at least nine different members of the ClC family of chloride channels. So far only two of them could be localized on a cellular level in the kidney. We now report on the precise intrarenal localization of the mRNAs coding for the chloride channels ClC-2, ClC-3 and ClC-5. Expression of ClC-2 mRNA, encoding a swelling-activated chloride channel, could be demonstrated in the S3 segment of the proximal tubule. The chloride channel ClC-3 mRNA and ClC-5 mRNA, coding for a chloride channel mutated in kidney stone disease, were both expressed in intercalated cells of the connecting tubule and collecting duct. Whereas ClC-3 mRNA expression was most prominent in the cortex of rat kidneys, ClC-5 mRNA was expressed from the cortex through the upper portion of the inner medulla. A detailed analysis revealed that ClC-3 was expressed by type B intercalated cells, whereas ClC-5 was expressed by type A intercalated cells. These findings have important implications for the pathogenesis of hereditary kidney stone disease caused by mutations in the CLCN5 gene.

摘要

哺乳动物基因组编码氯化物通道ClC家族的至少九个不同成员。到目前为止,其中只有两个能够在细胞水平上定位于肾脏。我们现在报告编码氯化物通道ClC-2、ClC-3和ClC-5的mRNA在肾脏内的精确定位。编码肿胀激活氯化物通道的ClC-2 mRNA的表达可在近端小管的S3段中得到证实。编码在肾结石疾病中发生突变的氯化物通道的氯化物通道ClC-3 mRNA和ClC-5 mRNA均在连接小管和集合管的闰细胞中表达。虽然ClC-3 mRNA表达在大鼠肾脏皮质中最为显著,但ClC-5 mRNA从皮质到内髓质上部均有表达。详细分析显示,ClC-3由B型闰细胞表达,而ClC-5由A型闰细胞表达。这些发现对由CLCN5基因突变引起的遗传性肾结石疾病的发病机制具有重要意义。

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