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首页> 外文期刊>American Journal of Physiology >Avian renal proximal tubule epithelium urate secretion is mediated by Mrp4
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Avian renal proximal tubule epithelium urate secretion is mediated by Mrp4

机译:禽肾近端小管上皮尿液分泌由MRP4介导

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Avian renal proximal tubule epithelium urate secretion is mediated by Mrp4. Am J Physiol Regul Integr Comp Physiol 295: R2024-R2033, 2008. First published October 22, 2008; doi: 10.1152/ajpregu.9O471.2008.-Birds are uri-cotehc and, like humans, maintain high plasma urate concentrations (~300 (xM). The majority of their urate waste, as in humans, is eliminated by renal proximal tubular secretion; however, the mechanism of urate transport across the brush-border membrane of the intact proximal tubule epithelium during secretion is uncertain. The dominance of secretory urate transport in the bird provides a convenient model for examining this process. The present study shows that short hairpin RNA interference (shRNAi) effectively knocked down gene expression of multidrug resistance protein 4 (Mrp4; 25% of control) in primary monolayer cultures of isolated chicken proximal tubule epithelial cells (cPTCs). Control and Mrp4-shRNAi-treated cPTCs were mounted in Ussing chambers and unidirectional transepithelial fluxes of urate were measured. To detect nonspecific effects, transepithelial electrical resistance (TER) and sodium-dependent glucose transport (Igiu) were monitored throughout experiments. Knocking down Mrp4 expression resulted in a reduction of transepithelial urate secretion to 35% of control with no effects on TER or Iglu. Although electrical gradient-driven urate transport in isolated brush-border membrane vesicles was confirmed, potassium-induced depolarization of the plasma membrane in intact cPTCs failed to inhibit active transepithelial urate secretion. However, electrical gradient-dependent vesicular urate transport was inhibited by the MRP4 inhibitor MK-571 also known to inhibit active transepithelial urate transport by cPTCs. Based on these data, direct measure of active transepithelial urate secretion in functional avian proximal tubule epithelium indicates that Mrp4 is the dominant apical membrane exit pathway from cell to lumen
机译:禽肾近端管上皮尿液分泌由MRP4介导。 AM J Physiol Study Intend Comp Physiol 295:R2024-R2033,2008。2008年10月22日第一次出版; DOI:10.1152 / AJPREGU.9O471.2008.-鸟类是URI-COTEEHC,如人,保持高血浆尿液浓度(〜300(XM)。作为人类的大多数呼吸废物,被肾近端丢失分泌物;然而,分泌过程中完整的近端小管上皮细胞上皮细胞刷膜的呼吸覆盖机制是不确定的。鸟类中分泌口运输的主导地位为检查该过程提供了方便的模型。本研究表明较短发夹RNA干扰(SHRNAI)在分离的鸡近端小管上皮细胞(CPTCs)的主要单层培养中有效地击落了多药抗性蛋白4(MRP4; 25%对照)的基因表达。对照和MRP4-SHRNAI处理的CPTC安装在测量了uSSing腔室和单向性的调节尿液。以检测非特异性效应,抗脑梗阻电阻(TER)和依赖依赖性葡萄糖输送(IGIU)在整个实验中被监测。击败MRP4表达导致TRANSEPERELIAL SICTE分泌减少到35%的对照,对TER或IGLU没有影响。尽管确认了隔离刷边膜囊泡中的电梯度驱动的呼吸物,但在完整的CPTC中诱导钾诱导的血浆膜的去极化未能抑制活性的Transepelial口腔分泌。然而,通过CPTC抑制活性Transepearlial尿剂转运,MRP4抑制剂MK-571抑制了电梯度依赖性尿酸尿剂量。基于这些数据,在功能性禽近端小管上皮中的活性TransepeLELIAL口腔分泌的直接测量表明MRP4是从细胞到腔的主导顶端膜出口途径

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