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RPTEC/TERT1细胞系作为体外肾毒性评估的改良工具。

The RPTEC/TERT1 Cell Line as an Improved Tool for In Vitro Nephrotoxicity Assessments.

作者信息

Simon-Friedt Bridget R, Wilson Mark J, Blake Diane A, Yu Haini, Eriksson Yasmin, Wickliffe Jeffrey K

机构信息

Graduate Program in Biomedical Sciences, Tulane University School of Medicine, New Orleans, LA, 70112, USA.

出版信息

Biol Trace Elem Res. 2015 Jul;166(1):66-71. doi: 10.1007/s12011-015-0339-y. Epub 2015 Apr 19.

Abstract

In earlier studies, we have characterized a newly developed cell line derived from the renal proximal tubule epithelial cells (RPTEC) of a healthy human male donor in order to provide an improved in vitro model with which to investigate human diseases, such as cancer, that may be promoted by toxicant exposure. The RPTEC/TERT1 cell line has been immortalized using the human telomerase reverse transcriptase (hTERT) catalytic subunit and does not exhibit chromosomal abnormalities (Evercyte Laboratories). We have previously conducted single-compound and binary mixture experiments with the common environmental carcinogens, cadmium (Cd), and benzo[a]pyrene (B[a]P). Cells exhibited cytotoxic and compound-specific responses to low concentrations of B[a]P and Cd. We detected responses after exposure consistent with what is known regarding these cells in a normal, healthy kidney including significant gene expression changes, BPDE-DNA adducts in the presence of B[a]P, and indications of oxidative stress in the presence of Cd. The RPTEC/TERT1 cell line was also amenable to co-exposure studies due to its sensitivity and compound-specific properties. Here, we review our earlier work, compare our findings with commonly used renal cell lines, and suggest directions for future experiments. We conclude that the RPTEC/TERT1 cell line can provide a useful tool for future toxicological and mixture studies.

摘要

在早期研究中,我们对源自一名健康男性供体的肾近端小管上皮细胞(RPTEC)的新开发细胞系进行了表征,以便提供一个改进的体外模型,用于研究可能因接触毒物而引发的人类疾病,如癌症。RPTEC/TERT1细胞系已使用人端粒酶逆转录酶(hTERT)催化亚基进行了永生化处理,且未表现出染色体异常(埃弗西特实验室)。我们之前用常见的环境致癌物镉(Cd)和苯并[a]芘(B[a]P)进行了单化合物和二元混合物实验。细胞对低浓度的B[a]P和Cd表现出细胞毒性和化合物特异性反应。在接触后,我们检测到的反应与正常健康肾脏中这些细胞的已知情况一致,包括显著的基因表达变化、在有B[a]P存在时的BPDE-DNA加合物,以及在有Cd存在时的氧化应激迹象。由于其敏感性和化合物特异性特性,RPTEC/TERT1细胞系也适用于共暴露研究。在此,我们回顾我们早期的工作,将我们的发现与常用的肾细胞系进行比较,并提出未来实验的方向。我们得出结论,RPTEC/TERT1细胞系可为未来的毒理学和混合物研究提供一个有用的工具。

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