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Novel conditionally immortalized human proximal tubule cell line expressing functional influx and efflux transporters

机译:表达功能性内向和外向转运蛋白的新型条件永生化人类近端肾小管细胞系

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Reabsorption of filtered solutes from the glomerular filtrate and excretion of waste products and xenobiotics are the main functions of the renal proximal tubular (PT) epithelium. A human PT cell line expressing a range of functional transporters would help to augment current knowledge in renal physiology and pharmacology. We have established and characterized a conditionally immortalized PT epithelial cell line (ciPTEC) obtained by transfecting and subcloning cells exfoliated in the urine of a healthy volunteer. The PT origin of this line has been confirmed morphologically and by the expression of aminopeptidase N, zona occludens 1, aquaporin 1, dipeptidyl peptidase IV and multidrug resistance protein 4 together with alkaline phosphatase activity. ciPTEC assembles in a tight monolayer with limited diffusion of inulin-fluorescein-isothiocyanate. Concentration and time-dependent reabsorption of albumin via endocytosis has been demonstrated, together with sodium-dependent phosphate uptake. The expression and activity of apical efflux transporter p-glycoprotein and of baso-lateral influx transporter organic cation transporter 2 have been shown in ciPTEC. This established human ciPTEC expressing multiple endogenous organic ion transporters mimicking renal reabsorption and excretion represents a powerful tool for future in vitro transport studies in pharmacology and physiology. Keywords Proximal tubule cell - Albumin endocytosis - Phosphate transport - Organic cation transport - P-glycoprotein - Human Cystinosis Research Foundation, Cystinosis Research Network and European Community’s Seventh Framework Programme (FP7/2007-2013, grant agreement n° 201590) are acknowledged for their financial support.
机译:肾小球滤过液中溶质的重吸收以及废物和异生物素的排泄是肾近端肾小管上皮的主要功能。表达一系列功能性转运蛋白的人PT细胞系将有助于增加对肾脏生理学和药理学的当前知识。我们已经建立并表征了通过转染和亚克隆健康志愿者尿液中脱落的细胞而获得的有条件永生的PT上皮细胞系(ciPTEC)。该品系的PT起源已在形态上得到了证实,并且通过表达氨基肽酶N,透明带遮盖物1,水通道蛋白1,二肽基肽酶IV和多药耐药蛋白4以及碱性磷酸酶的活性得以证实。 ciPTEC组装成紧密的单层,且菊粉-荧光素-异硫氰酸酯的扩散受限。已经证明通过内吞作用浓度和时间依赖性重吸收白蛋白,以及钠依赖性磷酸盐摄取。 ciPTEC中已显示了根尖外向转运蛋白p-糖蛋白和基底外侧流入转运蛋白有机阳离子转运蛋白2的表达和活性。这种建立的表达多种内源性有机离子转运蛋白的人ciPTEC模仿了肾脏的重吸收和排泄,是未来药理和生理学体外转运研究的有力工具。关键词近端肾小管细胞-白蛋白内吞作用-磷酸盐运输-有机阳离子运输-P-糖蛋白-人类胱氨酸病研究基金会,胱氨酸病研究网络和欧洲共同体第七框架计划(FP7 / 2007-2013,拨款协议编号201590)经济支持。

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