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首页> 外文期刊>Kidney international. >Putative subunits of the rat mesangial KATP: A type 2B sulfonylurea receptor and an inwardly rectifying K|[plus]| channel
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Putative subunits of the rat mesangial KATP: A type 2B sulfonylurea receptor and an inwardly rectifying K|[plus]| channel

机译:大鼠肾小球系膜KATP的假定亚基:2B型磺酰脲受体和向内整流的K | [plus] |渠道

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Putative subunits of the rat mesangial KATP: A type 2B sulfonylurea receptor and an inwardly rectifying K+ channel.BackgroundSulfonylurea agents exert their physiological effects in many cell types via binding to specific sulfonylurea receptors (SUR). SUR couple to inwardly-rectifying K+ channel (Kir6.x) to form tetradimeric ATP-sensitive K+ channels (KATP). The SUR subunits confer ATP-sensitivity on KATP and also provide the binding sites for sulfonylureas and other pharmacological agents. Our previous work demonstrated that the exposure of mesangial cells (MC) to sulfonylureas generated profound effects on MC glucose uptake and matrix metabolism and induced heightened cell contractility in association with Ca2+ transients. Because these responses likely resulted from the binding of sulfonylurea to a mesangial SUR2, we subsequently documented [3H]-glibenclamide binding to MC and the gene expression of several mesangial SUR2 transcripts. From these data, we inferred that MC expressed the components of a mesangial KATP and sought to establish their presence in primary MC.
机译:大鼠肾小球系膜KATP的假定亚基:2B型磺酰脲受体和向内整流的K +通道。背景磺酰脲类药物通过与特定的磺酰脲类受体(SUR)结合,在许多细胞类型中发挥其生理作用。 SUR与向内整流的K +通道(Kir6.x)耦合以形成四聚体ATP敏感的K +通道(KATP)。 SUR亚基赋予KATP ATP敏感性,还提供了磺酰脲类和其他药理剂的结合位点。我们以前的工作表明,肾小球系膜细胞(MC)暴露于磺酰脲类对MC葡萄糖摄取和基质代谢产生了深远的影响,并引起与Ca2 +瞬变有关的细胞收缩性增强。因为这些反应可能是由于磺酰脲与肾小球系膜SUR2的结合所致,所以我们随后记录了[3H]-格列本脲与MC的结合以及几种肾小球系膜SUR2转录本的基因表达。从这些数据,我们推断MC表达了肾小球系膜KATP的成分,并试图确定它们在原发性MC中的存在。

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