Laboratory of Molecular Nutrition and Toxicology, Faculty of Pharmaceutical Sciences, Tokushima Bunri University.
J Toxicol Sci. 2019;44(9):611-619. doi: 10.2131/jts.44.611.
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 Cd and Mn from apical sides were the highest in S3 cells, and Cd, Mn, and Zn mutually inhibited the apical uptake of each metal. As the expression of ZIP8, a zinc transporter having affinities for Cd and Mn, was the highest in S3 cells, ZIP8 may contribute largely to the apical uptakes of these metals. The efficient uptake of Mn 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.
肾脏近端小管是许多肾毒物的靶标,包括镉 (Cd),也是肾小球滤液中必需金属重吸收到全身循环的部位。虽然卷曲状近端小管(S1 和 S2 段)和直形近端小管(S3 段)中的金属转运机制可能不同,但对金属转运的特定节段模式知之甚少。在这里,我们利用源自小鼠肾脏近端小管 S1、S2 和 S3 段的永生化细胞系,使用 Trans-well 培养系统检查 Cd 和锰 (Mn) 的特定节段和方向依赖性转运。结果表明,S3 细胞从顶端侧摄取 Cd 和 Mn 的量最高,Cd、Mn 和 Zn 相互抑制每种金属的顶端摄取。由于锌转运蛋白 ZIP8 的表达在 S3 细胞中最高,对 Cd 和 Mn 具有亲和力,ZIP8 可能对这些金属的顶端摄取有很大贡献。S3 细胞从顶端侧有效摄取 Mn 可能表明 ZIP8 在近端小管中对 Mn(一种必需金属)的重吸收中起重要作用。我们的研究表明,S1、S2 和 S3 细胞为研究肾脏近端小管中有毒和必需金属的特定节段和方向依赖性转运提供了有用的工具。