利用高通量CometChip平台评估体外三维HepaRG球形模型的遗传毒性测试。

ALTEX Pub Date : 2022-01-01 Epub Date: 2022-03-18 DOI:10.14573/altex.2201121
Ji-Eun Seo, Xiaobo He, Levan Muskhelishvili, Pritpal Malhi, Nan Mei, Mugimane Manjanatha, Matthew Bryant, Tong Zhou, Timothy Robison, Xiaoqing Guo
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引用次数: 9

摘要

三维(3D)培养系统越来越多地用于遗传毒性研究,因为改进了细胞间相互作用和组织样结构,这些在二维培养中是有限的或缺乏的。本研究利用具有代谢能力的HepaRG细胞优化了3D培养系统,用于体外遗传毒性测试。在96孔或384孔的超低附着板上形成3D HepaRG球体,将其暴露于不同浓度的34种测试物中,包括8种直接作用和11种间接作用的基因毒物/致癌物,以及15种在体外和体内表现出不同基因毒性反应的化合物。在2D和3D培养中,采用高通量CometChip法评估DNA损伤,同时采用ATP法评估细胞毒性。3D HepaRG球体保持稳定表型长达30天,与2D培养相比,白蛋白分泌水平更高,细胞色素P450基因表达水平更高,酶活性也更高。3D球体在检测直接和间接作用的基因毒性/致癌物方面也表现出比2D培养更高的灵敏度,表明可以更好地预测体内遗传毒性反应。当使用PROAST软件量化DNA损伤剂量-反应数据时,与2D HepaRG细胞相比,3D球体通常具有更低或相似的基准剂量值,并且与原代人肝细胞更具可比性。这些结果表明,3D模型可以适应CometChip技术进行高通量遗传毒性测试,3D HepaRG球体可以作为一种可靠和实用的体外方法,更好地支持潜在人类遗传毒性致癌物的危害识别和风险评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of an in vitro three-dimensional HepaRG spheroid model for genotoxicity testing using the high-throughput CometChip platform.

Three-dimensional (3D) culture systems are increasingly being used for genotoxicity studies due to improved cell-to-cell interactions and tissue-like structures that are limited or lacking in 2D cultures. The present study optimized a 3D culture system using metabolically competent HepaRG cells for in vitro genotoxicity testing. 3D HepaRG spheroids, formed in 96- or 384-well ultra-low attachment plates, were exposed to various concentrations of 34 test articles, including 8 direct-acting and 11 indirect-acting genotoxicants/carcinogens as well as 15 compounds that show different genotoxic responses in vitro and in vivo. DNA damage was evaluated using the high-throughput CometChip assay with con-current cytotoxicity assessment by the ATP assay in both 2D and 3D cultures. 3D HepaRG spheroids maintained a stable phenotype for up to 30 days with higher levels of albumin secretion, cytochrome P450 gene expression, and enzyme activities compared to 2D cultures. 3D spheroids also demonstrated a higher sensitivity than 2D cultures for detecting both direct- and indirect-acting genotoxicants/carcinogens, indicating a better prediction of in vivo genotoxicity responses. When DNA damage dose-response data were quantified using PROAST software, 3D spheroids generally had lower or similar benchmark dose values compared to 2D HepaRG cells and were more comparable with primary human hepatocytes. These results demonstrate that 3D models can be adapted to the CometChip technology for high-throughput genotoxicity testing and that 3D HepaRG spheroids may be used as a reliable and pragmatic in vitro approach to better support the hazard identification and risk assessment of potential human genotoxic carcinogens.

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