Fraunhofer Project Group PZ-Syn, Fraunhofer Institute for Cell Therapy and Immunology, Branch Bioanalytics and Bioprocesses (IZI-BB) Located at the Institute of Biotechnology, Brandenburg University of Technology Cottbus-Senftenberg, Senftenberg, Germany.
Institute of Biotechnology, Brandenburg University of Technology Cottbus-Senftenberg, Senftenberg, Germany.
Cells. 2023 Aug 24;12(17):2140. doi: 10.3390/cells12172140.
In the liver, phase-1 biotransformation of drugs and other xenobiotics is largely facilitated by enzyme complexes consisting of cytochrome P450 oxidoreductase (CPR) and cytochrome P450 monooxygenases (CYPs). Generated from human liver-derived cell lines, recombinant in vitro cell systems with overexpression of defined phase-1 enzymes are widely used for pharmacological and toxicological drug assessment and laboratory-scale production of drug-specific reference metabolites. Most, if not all, of these cell lines, however, display some background activity of several CYPs, making it difficult to attribute effects to defined CYPs. The aim of this study was to generate cell lines with stable overexpression of human phase-1 enzymes based on Chinese hamster ovary (CHO) suspension cells. Cells were sequentially modified with cDNAs for human CPR in combination with CYP1A2, CYP2B6, or CYP3A4, using lentiviral gene transfer. In parallel, CYP-overexpressing cell lines without recombinant CPR were generated. Successful recombinant expression was demonstrated by mRNA and protein analyses. Using prototypical CYP-substrates, generated cell lines proved to display specific enzyme activities of each overexpressed CYP while we did not find any endogenous activity of those CYPs in parental CHO cells. Interestingly, cell lines revealed some evidence that the dependence of CYP activity on CPR could vary between CYPs. This needs to be confirmed in further studies. Recombinant expression of CPR was also shown to enhance CYP3A4-independent metabolisation of testosterone to androstenedione in CHO cells. We propose the novel serum-free CHO suspension cell lines with enhanced CPR and/or defined CYP activity as a promising "humanised" in vitro model to study the specific effects of those human CYPs. This could be relevant for toxicology and/or pharmacology studies in the pharmaceutical industry or medicine.
在肝脏中,药物和其他外源性物质的 I 相生物转化主要由细胞色素 P450 氧化还原酶(CPR)和细胞色素 P450 单加氧酶(CYPs)组成的酶复合物来促进。从人肝源性细胞系产生的、过表达特定 I 相酶的重组体外细胞系统广泛用于药理学和毒理学药物评估以及药物特异性参考代谢物的实验室规模生产。然而,这些细胞系中的大多数(如果不是全部的话)都显示出几种 CYP 的一些背景活性,使得难以将效应归因于特定的 CYP。本研究的目的是基于中国仓鼠卵巢(CHO)悬浮细胞生成具有稳定过表达人 I 相酶的细胞系。细胞依次用 cDNA 修饰,以与 CYP1A2、CYP2B6 或 CYP3A4 共表达,使用慢病毒基因转移。同时,生成了没有重组 CPR 的 CYP 过表达细胞系。通过 mRNA 和蛋白质分析证明了成功的重组表达。使用原型 CYP 底物,生成的细胞系被证明显示出每个过表达 CYP 的特异性酶活性,而我们在亲本 CHO 细胞中没有发现这些 CYP 的任何内源性活性。有趣的是,细胞系显示出一些证据表明 CYP 活性对 CPR 的依赖性可能在 CYP 之间有所不同。这需要在进一步的研究中得到证实。CPR 的重组表达也被证明可以增强 CHO 细胞中睾酮向雄烯二酮的 CYP3A4 非依赖性代谢。我们提出了新型的无血清 CHO 悬浮细胞系,具有增强的 CPR 和/或定义的 CYP 活性,作为研究这些人 CYP 特定效应的有前途的“人源化”体外模型。这可能与制药行业或医学中的毒理学和/或药理学研究相关。