Xia Lei, Hong Xin, Sakban Rashidah Binte, Qu Yinghua, Singh Nisha Hari, McMillian Michael, Dallas Shannon, Silva Jose, Sensenhauser Carlo, Zhao Sylvia, Lim Heng Keang, Yu Hanry
Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, MD9-04-11, 2 Medical Drive, 117597, Singapore.
Institute of Bioengineering and Nanotechnology, A*STAR, The Nanos, #04-01, 31 Biopolis Way, 138669, Singapore.
J Appl Toxicol. 2016 Feb;36(2):320-9. doi: 10.1002/jat.3189. Epub 2015 Jul 21.
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.
细胞色素P450(CYP)诱导是临床药物相互作用的关键风险因素,在药物发现的早期阶段必须加以缓解。与传统的二维(2D)单层培养相比,体外肝细胞的三维(3D)培养最近已成为一种潜在的更好平台,可重现体内肝脏结构并维持长期肝功能。然而,大多数已发表的关于3D肝细胞模型的研究使用大鼠肝细胞,并且啮齿动物和人类对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拴系球体作为体外3D模型。拴系球体中CYP3A4 mRNA表达的诱导程度明显高于胶原夹心培养中的表达,表明转录调控在3D模型中对CYP诱导剂更敏感。拴系球体中CYP1A2、CYP2B6和CYP3A4活性的诱导与胶原夹心培养中观察到的活性相当,甚至更高。基于膜的模型很容易整合到多孔板中用于高通量药物测试应用,这可能是一种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。