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首页> 外文期刊>American Journal of Physiology >Plasma membrane Ca2+-ATPase and NCX1 Na+/Ca2+ exchanger expression in distal convoluted tubule cells.
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Plasma membrane Ca2+-ATPase and NCX1 Na+/Ca2+ exchanger expression in distal convoluted tubule cells.

机译:远曲小管细胞中的质膜Ca2 + -ATPase和NCX1 Na + / Ca2 +交换子表达。

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摘要

The plasma membrane Ca2+-ATPase (PMCA) and the NCX1 Na+/Ca2+ exchanger regulate intracellular Ca2+ concentrations and mediate Ca2+ efflux in absorptive epithelial cells. We characterized the PMCA isoforms and subtypes expressed in mouse distal convoluted tubule (mDCT) cells and Na+/Ca2+ exchanger protein expression in mDCT cells. In lysates of mDCT cells, immunoprecipitation and Western blot analysis, performed with a monoclonal antibody to PMCA, revealed a 140-kDa protein consistent with PMCA. Laser-scanning confocal fluorescence microscopy indicated that PMCA and NCX1 expression is restricted to basolateral membranes only in confluent mDCT cells, because subconfluent cultures predominately express intracellular localizations. PMCA isoform-specific PCR primers generated appropriately sized products only for PMCA1 and PMCA4 from DCT cells but PMCA1-4 from whole mouse kidney. Assessment of splice site C within the calmodulin-binding domain demonstrated the presence of PMCA1b and PMCA4b mRNAs in mDCT cells. Northern blot analysis of mDCT cell RNA revealed transcripts of 7.5 and 5.5 kb for PMCA1 and 8.5 and 7.5 kb for PMCA4. We conclude that DCT cells express PMCA transcripts encoding PMCA1b and PMCA4b. Basolateral localization of the Na+/Ca2+ exchanger and MCAs support the idea that multiple PMCA isoforms, in concert with the Na+/Ca2+ exchanger, mediate basal or hormone-stimulated Ca2+ efflux by distal tubules.
机译:质膜Ca2 + -ATPase(PMCA)和NCX1 Na + / Ca2 +交换剂调节细胞内Ca2 +浓度并介导吸收性上皮细胞中的Ca2 +外排。我们表征了在小鼠远曲小管(mDCT)细胞中表达的PMCA亚型和亚型,并在mDCT细胞中表达了Na + / Ca2 +交换蛋白。在mDCT细胞的裂解物中,用针对PMCA的单克隆抗体进行的免疫沉淀和蛋白质印迹分析显示与PMCA一致的140 kDa蛋白。激光扫描共聚焦荧光显微镜检查表明,PMCA和NCX1表达仅在汇合的mDCT细胞中局限于基底外侧膜,因为亚汇合的培养物主要表达细胞内定位。 PMCA同工型特异性PCR引物仅从DCT细胞中为PMCA1和PMCA4产生适当大小的产物,而从整个小鼠肾脏中产生PMCA1-4。钙调蛋白结合域内的剪接位点C的评估表明mDCT细胞中存在PMCA1b和PMCA4b mRNA。对mDCT细胞RNA的Northern印迹分析显示,PMCA1的转录本为7.5和5.5 kb,PMCA4的转录本为8.5和7.5 kb。我们得出结论,DCT细胞表达编码PMCA1b和PMCA4b的PMCA转录本。 Na + / Ca2 +交换子和MCA的基底外侧定位支持以下想法:多个PMCA亚型与Na + / Ca2 +交换子协同,通过远端小管介导基础或激素刺激的Ca2 +外排。

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