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钠-钾-氯协同转运蛋白

The Na-K-Cl cotransporters.

作者信息

Haas M

机构信息

Department of Pathology, University of Chicago, Illinois 60637.

出版信息

Am J Physiol. 1994 Oct;267(4 Pt 1):C869-85. doi: 10.1152/ajpcell.1994.267.4.C869.

DOI:10.1152/ajpcell.1994.267.4.C869
PMID:7943281
Abstract

The Na-K-Cl cotransporters are a class of membrane proteins that transport Na, K, and Cl ions into and out of cells in an electrically neutral manner, in most cases with a stoichiometry of 1Na:1K:2Cl. Na-K-Cl cotransporters are present in a wide variety of cells and tissues, including reabsorptive and secretory epithelia, nerve and muscle cells, endothelial cells, fibroblasts, and blood cells. Na-K-Cl cotransport plays a vital role in renal salt reabsorption and in salt secretion by intestinal, airway, salivary gland, and other secretory epithelia. Cotransport function also appears to be important in the maintenance and regulation of cell volume and of ion gradients by both epithelial and nonepithelial cells. Na-K-Cl cotransport activity is inhibited by "loop" diuretics, including the clinically efficacious agents bumetanide and furosemide. The regulation of Na-K-Cl cotransport is mediated, at least in some cases, through direct phosphorylation of the cotransport protein. Cotransporter regulation is highly tissue specific, perhaps in part related to the presence of different Na-K-Cl cotransporter isoforms. In epithelia, both absorptive (kidney-specific) and secretory isoforms have been identified by cDNA cloning and sequencing and Northern blot analysis; alternatively spliced variants of the kidney-specific isoform have also been identified. The absorptive and secretory isoforms exhibit approximately 60% identity at the amino acid sequence level; these sequences in turn show approximately 45% overall homology with those of thiazide-sensitive, bumetanide-insensitive, Na-Cl cotransport proteins of winter flounder urinary bladder and mammalian kidney. This review focuses on recent developments in the identification of Na-K-Cl cotransport proteins in epithelial and on the regulation of epithelial Na-K-Cl cotransporter function at cellular and molecular levels.

摘要

钠-钾-氯共转运体是一类膜蛋白,能以电中性方式将钠、钾和氯离子转运进细胞或转运出细胞,在大多数情况下,其化学计量比为1钠:1钾:2氯。钠-钾-氯共转运体存在于多种细胞和组织中,包括重吸收和分泌性上皮细胞、神经和肌肉细胞、内皮细胞、成纤维细胞和血细胞。钠-钾-氯共转运在肾脏盐重吸收以及肠道、气道、唾液腺和其他分泌性上皮细胞的盐分泌中起着至关重要的作用。共转运功能在维持和调节上皮细胞和非上皮细胞的细胞体积及离子梯度方面似乎也很重要。钠-钾-氯共转运活性受到“袢”利尿剂的抑制,包括临床有效的药物布美他尼和呋塞米。钠-钾-氯共转运的调节至少在某些情况下是通过共转运蛋白的直接磷酸化介导的。共转运体调节具有高度的组织特异性,这可能部分与不同的钠-钾-氯共转运体亚型的存在有关。在上皮细胞中,通过cDNA克隆、测序和Northern印迹分析已鉴定出吸收性(肾脏特异性)和分泌性亚型;还鉴定出了肾脏特异性亚型的可变剪接变体。吸收性和分泌性亚型在氨基酸序列水平上具有约60%的同一性;这些序列与冬比目鱼膀胱和哺乳动物肾脏中对噻嗪类敏感、对布美他尼不敏感的钠-氯共转运蛋白的序列总体同源性约为45%。本综述重点关注上皮细胞中钠-钾-氯共转运蛋白鉴定的最新进展以及细胞和分子水平上上皮钠-钾-氯共转运体功能的调节。

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