首页> 外文期刊>Urological research >Human umbilical vein endothelial cells accelerate oxalate-induced apoptosis of human renal proximal tubule epithelial cells in co-culture system which is prevented by pyrrolidine dithiocarbamate
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Human umbilical vein endothelial cells accelerate oxalate-induced apoptosis of human renal proximal tubule epithelial cells in co-culture system which is prevented by pyrrolidine dithiocarbamate

机译:人脐静脉内皮细胞在共培养系统中加速草酸盐诱导的人肾近端肾小管上皮细胞凋亡,吡咯烷二硫代氨基甲酸酯可以防止

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摘要

Oxalate is the most common component of kidney stones and elevated urinary levels induce renal tubular cell toxicity and death which is essential for crystal attachment. Endothelial cells, in some studies have been shown to regulate certain functions of renal proximal tubule cells. The aim of this study was to evaluate the effect of endothelial cells on tubular cell apoptosis in a coculture system mimicking the in vivo renal physiological settings. The human umbilical vein endothelial cells (HUVEC) and human renal proximal tubule epithelial cells (RPTEC) were exposed to increasing concentrations (0-1.0 mM) of oxalate with or without 10 μM PDTC pretreatment for 24 h. In HUVEC, RPTEC and HUVEC-RPTEC co-cultures, the cell viability was measured using the WST-1 assay and cell death with the TUNEL analysis using the flow cytometry. The treatment of RPTECs with oxalate lead to 8.9-26.2% cell death which was reduced to 0-1.6% with the PDTC pretreatment. The death rate of RPTECs was significantly increased by 15-19% at different oxalate concentrations when co-cultured with HUVECs. In contrast, cell viability was not substantially altered in PDTC pretreated RPTECs that were co-cultured with HUVECs. Apoptosis was the way of cell death as similar rate of apoptosis was observed in cell culture systems. Although cell viability of RPTECs was further reduced when co-cultured with HUVECs, it was restored with the pretreatment of PDTC. This is the first study focusing on the role of endothelial cells on RPTEC apoptosis following hyperoxaluria.
机译:草酸盐是肾结石最常见的成分,尿液水平升高会引起肾小管细胞毒性和死亡,这对于晶体附着至关重要。在一些研究中,内皮细胞已证明可调节肾近端小管细胞的某些功能。这项研究的目的是评估模拟体内肾脏生理环境的共培养系统中内皮细胞对肾小管细胞凋亡的影响。在有或没有10μMPDTC预处理的情况下,将人脐静脉内皮细胞(HUVEC)和人肾近端小管上皮细胞(RPTEC)暴露于浓度递增(0-1.0 mM)的草酸盐中24小时。在HUVEC,RPTEC和HUVEC-RPTEC共培养物中,使用WST-1测定法测量细胞活力,并使用流式细胞仪通过TUNEL分析法测量细胞死亡。用草酸盐处理RPTECs可以导致8.9-26.2%的细胞死亡,而PDTC预处理可以将其降低到0-1.6%。与HUVEC共培养时,在不同草酸盐浓度下,RPTECs的死亡率显着提高了15-19%。相比之下,在与HUVEC共培养的PDTC预处理的RPTEC中,细胞活力并未发生实质性改变。凋亡是细胞死亡的方式,因为在细胞培养系统中观察到相似的凋亡率。尽管与HUVECs共培养时RPTECs的细胞活力进一步降低,但通过PDTC的预处理可以恢复其活力。这是首次研究高草酸尿后内皮细胞在RPTEC凋亡中的作用。

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