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系统定量分析哺乳动物细胞中的群体细胞死亡动力学。

Systematic Quantification of Population Cell Death Kinetics in Mammalian Cells.

机构信息

Department of Biology, Stanford University, Room 104, 337 Campus Drive, Stanford, CA 94305, USA.

Department of Biology, Stanford University, Room 104, 337 Campus Drive, Stanford, CA 94305, USA.

出版信息

Cell Syst. 2017 Jun 28;4(6):600-610.e6. doi: 10.1016/j.cels.2017.05.002. Epub 2017 Jun 7.

Abstract

Cytotoxic compounds are important drugs and research tools. Here, we introduce a method, scalable time-lapse analysis of cell death kinetics (STACK), to quantify the kinetics of compound-induced cell death in mammalian cells at the population level. STACK uses live and dead cell markers, high-throughput time-lapse imaging, and mathematical modeling to determine the kinetics of population cell death over time. We used STACK to profile the effects of over 1,800 bioactive compounds on cell death in two human cancer cell lines, resulting in a large and freely available dataset. 79 potent lethal compounds common to both cell lines caused cell death with widely divergent kinetics. 13 compounds triggered cell death within hours, including the metallophore zinc pyrithione. Mechanistic studies demonstrated that this rapid onset lethal phenotype was caused in human cancer cells by metabolic disruption and ATP depletion. These results provide the first comprehensive survey of cell death kinetics and analysis of rapid-onset lethal compounds.

摘要

细胞毒性化合物是重要的药物和研究工具。在这里,我们介绍了一种方法,即可扩展的细胞死亡动力学实时分析(STACK),用于在哺乳动物细胞群体水平上定量测定化合物诱导的细胞死亡动力学。STACK 使用活细胞和死细胞标记物、高通量实时成像和数学建模来确定随时间推移的群体细胞死亡动力学。我们使用 STACK 对两种人类癌细胞系中 1800 多种生物活性化合物对细胞死亡的影响进行了分析,得到了一个大型且免费的数据集。79 种对两种细胞系均有效的有效致死化合物导致细胞死亡的动力学差异很大。13 种化合物在数小时内引发细胞死亡,其中包括金属载体吡啶硫酮锌。机制研究表明,这种快速起始的致死表型是由人类癌细胞中的代谢紊乱和 ATP 耗竭引起的。这些结果提供了对细胞死亡动力学的全面调查和对快速起始致死化合物的分析。

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