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