首页> 外文期刊>The Journal of toxicological sciences >Segment-specific and direction-dependent transport of cadmium and manganese in immortalized S1, S2, and S3 cells derived from mouse kidney proximal tubules
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Segment-specific and direction-dependent transport of cadmium and manganese in immortalized S1, S2, and S3 cells derived from mouse kidney proximal tubules

机译:镉和锰在源自小鼠肾近端小管的永生化S1,S2和S3细胞中的分段特异性和方向依赖性转运

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The kidney proximal tubule is a target of many renal toxicants, including cadmium (Cd), and also a place of reabsorption of essential metals in glomerular filtrate to systemic circulation. Although the mechanisms of metal transport in the convoluted proximal tubule (S1 and S2 segments) and the straight proximal tubule (S3 segment) may differ, little is known about the segment-specific modes of metal transport. Here, we utilized immortalized cell lines derived from the S1, S2, and S3 segments of mouse kidney proximal tubules, and examined the segment-specific and direction-dependent transport of Cd and manganese (Mn) using a trans-well culture system. The results showed that the uptakes of Cdsup2+/sup and Mnsup2+/sup from apical sides were the highest in S3 cells, and Cdsup2+/sup, Mnsup2+/sup, and Znsup2+/sup mutually inhibited the apical uptake of each metal. As the expression of ZIP8, a zinc transporter having affinities for Cdsup2+/sup and Mnsup2+/sup, was the highest in S3 cells, ZIP8 may contribute largely to the apical uptakes of these metals. The efficient uptake of Mnsup2+/sup from apical side of S3 cells may suggest an important role of ZIP8 in proximal tubule in reabsorption of Mn, an essential metal. Our study demonstrated that S1, S2, and S3 cells provide a useful tool for studying the segment-specific and direction-dependent transport of both toxic and essential metals in the kidney’s proximal tubules.
机译:肾近端小管是许多肾脏有毒物质(包括镉(Cd))的靶标,也是肾小球滤出液中必需金属重吸收到全身循环的场所。尽管在回旋的近端小管(S1和S2段)和笔直的近端小管(S3段)中金属运输的机制可能有所不同,但对于特定的金属运输方式知之甚少。在这里,我们利用源自小鼠肾近端小管的S1,S2和S3片段的永生细胞系,并使用跨孔培养系统检查了Cd和锰(Mn)的片段特异性和方向依赖性转运。结果表明,S3细胞的顶侧对Cd 2 + 和Mn 2 + 的吸收最高,而Cd 2 + Mn 2 + 和Zn 2 + 相互抑制每种金属的顶端吸收。由于ZIP8的表达在S3细胞中最高,锌转运蛋白具有Cd 2 + 和Mn 2 + 的亲和力,ZIP8可能在很大程度上促进了Zap8的根吸收。这些金属。从S3细胞顶侧有效吸收Mn 2 + 可能表明ZIP8在近端小管中对必需金属Mn的重吸收起着重要作用。我们的研究表明,S1,S2和S3细胞为研究肾近端小管中有毒金属和必需金属的片段特异性和方向依赖性转运提供了有用的工具。

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