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首页> 外文期刊>Journal of applied toxicology >Cytochrome P450 induction response in tethered spheroids as a three-dimensional human hepatocyte in vitro model
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Cytochrome P450 induction response in tethered spheroids as a three-dimensional human hepatocyte in vitro model

机译:系留球体中的细胞色素P450诱导应答作为三维人肝细胞体外模型

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摘要

Cytochrome P450 (CYP) induction is a key risk factor of clinical drug-drug interactions that has to be mitigated in the early phases of drug discovery. Three-dimensional (3D) cultures of hepatocytes in vitro have recently emerged as a potentially better platform to recapitulate the in vivo liver structure and to maintain long-term hepatic functions as compared with conventional two-dimensional (2D) monolayer cultures. However, the majority of published studies on 3D hepatocyte models use rat hepatocytes and the response to CYP inducers between rodents and humans is distinct. In the present study, we constructed tethered spheroids on RGD/galactose-conjugated membranes as an in vitro 3D model using cryopreserved human hepatocytes. CYP3A4 mRNA expression in the tethered spheroids was induced to a significantly greater extent than those in the collagen sandwich cultures, indicating the transcriptional regulation was more sensitive to the CYP inducers in the 3D model. Induction of CYP1A2, CYP2B6 and CYP3A4 activities in the tethered spheroids were comparable to, if not higher than that observed in the collagen sandwich cultures. The membrane-based model is readily integrated into multi-well plates for higher-throughput drug testing applications, which might be an alternative model to screen the CYP induction potential in vitro with more physiological relevance. Copyright (C) 2015 John Wiley & Sons, Ltd.
机译:细胞色素P450(CYP)的诱导是临床药物相互作用的关键危险因素,在药物发现的早期阶段必须减轻这种危险。与传统的二维(2D)单层培养相比,体外肝细胞的三维(3D)培养最近已成为潜在的更好的平台,可以概括体内肝脏结构并保持长期的肝功能。但是,关于3D肝细胞模型的大多数已发表研究都使用大鼠肝细胞,并且啮齿动物和人类之间对CYP诱导剂的反应是不同的。在本研究中,我们使用冷冻保存的人肝细胞在RGD /半乳糖共轭膜上构建了系链球体作为体外3D模型。 CYP3A4 mRNA的表达被束缚在球体中的程度明显大于胶原三明治培养物中的CYP3A4 mRNA的表达,表明在3D模型中转录调控对CYP诱导剂更敏感。拴系球体中CYP1A2,CYP2B6和CYP3A4活性的诱导作用与胶原三明治培养物中的诱导作用相当,甚至更高。基于膜的模型很容易集成到多孔板中,以进行更高通量的药物测试应用,这可能是在体外筛选具有更多生理相关性的CYP诱导潜力的替代模型。版权所有(C)2015 John Wiley&Sons,Ltd.

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