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Cell-based assay for the detection of chemically induced cellular stress by immortalized untransformed transgenic hepatocytes

机译:基于细胞的检测法用于永生化未转化的转基因肝细胞检测化学诱导的细胞应激

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摘要

BackgroundPrimary hepatocytes, one of the most widely used cell types for toxicological studies, have a very limited life span and must be freshly derived from mice or even humans. Attempts to use stable cell lines maintaining the enzymatic pattern of liver cells have been so far unsatisfactory. Stress proteins (heat shock proteins, HSPs) have been proposed as general markers of cellular injury and their use for environmental monitoring has been suggested. The aim of this work is to develop a bi-transgenic hepatocyte cell line in order to evaluate the ability of various organic and inorganic chemicals to induce the expression of the HSP70 driven reporter gene.We previously described transgenic mice (Hsp70/hGH) secreting high levels of human Growth Hormone (hGH) following exposure to toxic compounds in vivo and in vitro in primary cultures derived from different organs. In addition, we also reported another transgenic model (AT/cytoMet) allowing the reproducible immortalization of untransformed hepatocytes retaining in vitro complex liver functions.
机译:背景原代肝细胞是毒理学研究中使用最广泛的细胞类型之一,其寿命非常有限,必须从小鼠甚至人体内新鲜获得。迄今为止,尝试使用维持肝细胞酶促模式的稳定细胞系的方法并不令人满意。应激蛋白(热激蛋白,HSPs)已被提出作为细胞损伤的一般标志物,并被建议用于环境监测。这项工作的目的是开发一种双转基因肝细胞系,以评估各种有机和无机化学物质诱导HSP70驱动的报告基因表达的能力。我们先前描述了分泌高水平转基因小鼠(Hsp70 / hGH)体内和体外在源自不同器官的原代培养物中接触有毒化合物后人体生长激素(hGH)的水平。此外,我们还报道了另一种转基因模型(AT / cytoMet),允许未转化的肝细胞可再现地永生化,并具有体外复杂的肝功能。

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