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用于连续实时监测细胞毒性的自主生物发光哺乳动物细胞。

Autonomously bioluminescent mammalian cells for continuous and real-time monitoring of cytotoxicity.

作者信息

Xu Tingting, Close Dan M, Webb James D, Ripp Steven A, Sayler Gary S

机构信息

The Joint Institute for Biological Sciences, Oak Ridge National Laboratory.

出版信息

J Vis Exp. 2013 Oct 28(80):e50972. doi: 10.3791/50972.

Abstract

Mammalian cell-based in vitro assays have been widely employed as alternatives to animal testing for toxicological studies but have been limited due to the high monetary and time costs of parallel sample preparation that are necessitated due to the destructive nature of firefly luciferase-based screening methods. This video describes the utilization of autonomously bioluminescent mammalian cells, which do not require the destructive addition of a luciferin substrate, as an inexpensive and facile method for monitoring the cytotoxic effects of a compound of interest. Mammalian cells stably expressing the full bacterial bioluminescence (luxCDABEfrp) gene cassette autonomously produce an optical signal that peaks at 490 nm without the addition of an expensive and possibly interfering luciferin substrate, excitation by an external energy source, or destruction of the sample that is traditionally performed during optical imaging procedures. This independence from external stimulation places the burden for maintaining the bioluminescent reaction solely on the cell, meaning that the resultant signal is only detected during active metabolism. This characteristic makes the lux-expressing cell line an excellent candidate for use as a biosentinel against cytotoxic effects because changes in bioluminescent production are indicative of adverse effects on cellular growth and metabolism. Similarly, the autonomous nature and lack of required sample destruction permits repeated imaging of the same sample in real-time throughout the period of toxicant exposure and can be performed across multiple samples using existing imaging equipment in an automated fashion.

摘要

基于哺乳动物细胞的体外试验已被广泛用作毒理学研究中动物试验的替代方法,但由于基于萤火虫荧光素酶的筛选方法具有破坏性,需要进行平行样本制备,成本高昂且耗时,因此受到限制。本视频介绍了利用自主生物发光的哺乳动物细胞,这种细胞无需添加荧光素底物这种破坏性操作,作为一种监测目标化合物细胞毒性作用的廉价且简便的方法。稳定表达完整细菌生物发光(luxCDABEfrp)基因盒的哺乳动物细胞在不添加昂贵且可能产生干扰的荧光素底物、无需外部能量源激发或传统光学成像过程中对样本进行破坏的情况下,自主产生一个在490nm处达到峰值的光信号。这种不依赖外部刺激的特性使得维持生物发光反应的负担完全落在细胞上,这意味着只有在活跃代谢期间才能检测到产生的信号。这一特性使表达lux的细胞系成为用作细胞毒性作用生物哨兵的极佳候选者,因为生物发光产量的变化表明对细胞生长和代谢产生了不利影响。同样,其自主性和无需对样本进行破坏的特点允许在整个毒物暴露期间对同一样本进行实时重复成像,并且可以使用现有成像设备以自动化方式对多个样本进行成像。

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