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优化 HepaRG 细胞模型用于药物代谢和毒性研究。

Optimization of the HepaRG cell model for drug metabolism and toxicity studies.

机构信息

Inserm UMR 991, Rennes, France.

出版信息

Toxicol In Vitro. 2012 Dec;26(8):1278-85. doi: 10.1016/j.tiv.2012.05.008. Epub 2012 May 27.

Abstract

The HepaRG cell line is the first human cell line able to differentiate in vitro into mature hepatocyte-like cells. Our main objective within the framework of the EEC-LIINTOP project was to optimize the use of this cell line for drug metabolism and toxicity studies, especially after repeat treatments. The main results showed that differentiated HepaRG cells: (i) retained their drug metabolism capacity (major CYPs, phase 2 enzymes, transporters and nuclear receptors) and responsiveness to prototypical inducers at relatively stable levels for several weeks at confluence. The levels of several functions, including some CYPs such as CYP3A4, were dependent on the addition of dimethyl sulfoxide in the culture medium; (ii) sustained the different types of chemical-induced hepatotoxicity, including steatosis, phospholipidosis and cholestasis, after acute and/or repeat treatment with reference drugs. In particular, drug-induced vesicular steatosis was demonstrated in vitro for the first time. In conclusion, our results from the LIINTOP project, together with other studies reported concomitantly or more recently in the literature, support the conclusion that the metabolically competent human HepaRG cells represent a surrogate to primary human hepatocytes for investigating drug metabolism parameters and both acute and chronic effects of xenobiotics in human liver.

摘要

HepaRG 细胞系是第一个能够在体外分化为成熟肝样细胞的人类细胞系。我们在 EEC-LIINTOP 项目框架内的主要目标是优化该细胞系在药物代谢和毒性研究中的使用,特别是在重复治疗后。主要结果表明,分化的 HepaRG 细胞:(i)在汇合后数周内,以相对稳定的水平保留其药物代谢能力(主要 CYP、相 2 酶、转运体和核受体)和对原型诱导剂的反应性。包括一些 CYP 在内的几种功能的水平,如 CYP3A4,取决于培养基中二甲亚砜的添加;(ii)在急性和/或重复使用参考药物后,持续维持多种类型的化学诱导肝毒性,包括脂肪变性、磷脂沉积和胆汁淤积。特别是,首次在体外证明了药物诱导的囊泡脂肪变性。总之,我们在 LIINTOP 项目中的结果,以及同时或最近在文献中报告的其他研究结果,支持这样的结论,即代谢功能齐全的人 HepaRG 细胞是研究药物代谢参数以及外来物质在人肝中的急性和慢性作用的原代人肝细胞的替代物。

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