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使用 DMSO 分化的 HuH-7 细胞研究肝细胞色素 P450 3A4 抑制作用和肝毒性。

Study Liver Cytochrome P450 3A4 Inhibition and Hepatotoxicity Using DMSO-Differentiated HuH-7 Cells.

机构信息

Division of Toxicology, Office of Applied Research and Safety Assessment, Center for Food Safety and Applied Nutrition, U.S. Food and Drug Administration, Laurel, MD, USA.

出版信息

Methods Mol Biol. 2022;2474:39-46. doi: 10.1007/978-1-0716-2213-1_5.

Abstract

Metabolically competent, inexpensive, and robust in vitro cell models are needed for studying liver drug-metabolizing enzymes and hepatotoxicity. Human hepatoma HuH-7 cells develop into a differentiated in vitro model resembling primary human hepatocytes after a 2-week dimethyl sulfoxide (DMSO) treatment. DMSO-differentiated HuH-7 cells express elevated cytochrome P450 3A4 (CYP3A4) enzyme gene expression and activity compared to untreated HuH-7 cells. This cell model could be used to study CYP3A4 inhibition by reversible and time-dependent inhibitors, such as drugs, food ingredients, and environmental chemicals. The DMSO-differentiated HuH-7 model is also a suitable tool for investigating hepatotoxicity. This chapter describes a detailed methodology for developing DMSO-differentiated HuH-7 cells, which are subsequently used for CYP3A4 inhibition and hepatotoxicity studies.

摘要

需要具有代谢能力、成本低廉且稳健的体外细胞模型来研究肝脏药物代谢酶和肝毒性。用人肝癌 HuH-7 细胞经二甲基亚砜(DMSO)处理 2 周后,可分化为类似于原代人肝细胞的体外模型。与未经处理的 HuH-7 细胞相比,DMSO 分化的 HuH-7 细胞表达更高水平的细胞色素 P450 3A4(CYP3A4)酶基因表达和活性。该细胞模型可用于研究可逆和时间依赖性抑制剂(如药物、食物成分和环境化学品)对 CYP3A4 的抑制作用。DMSO 分化的 HuH-7 模型也是研究肝毒性的合适工具。本章介绍了一种详细的方法来开发 DMSO 分化的 HuH-7 细胞,随后可将其用于 CYP3A4 抑制和肝毒性研究。

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