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Non-invasive analysis of cell cycle dynamics in single living cells with Raman micro-spectroscopy.

机译:用拉曼光谱法对单个活细胞的细胞周期动力学进行非侵入性分析。

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Raman micro-spectroscopy is a laser-based technique which enables rapid and non-invasive biochemical analysis of cells and tissues without the need for labels, markers or stains. Previous characterization of the mammalian cell cycle using Raman micro-spectroscopy involved the analysis of suspensions of viable cells and individual fixed and/or dried cells. Cell suspensions do not provide cell-specific information, and fixing/drying can introduce artefacts which distort Raman spectra, potentially obscuring both qualitative and quantitative analytical results. In this article, we present Raman spectral characterization of biochemical changes related to cell cycle dynamics within single living cells in vitro. Raman spectra of human osteosarcoma cells synchronized in G(0)/G(1), S, and G(2)/M phases of the cell cycle were obtained and multivariate statistics applied to analyze the changes in cell spectra as a function of cell cycle phase. Principal components analysis identified spectral differences between cells in different phases, indicating a decrease in relative cellular lipid contribution to Raman spectral signatures from G(0)/G(1) to G(2)/M, with a concurrent relative increase in signal from nucleic acids and proteins. Supervised linear discriminant analysis of spectra was used to classify cells according to cell cycle phase, and exhibited 97% discrimination between G(0)/G(1)-phase cells and G(2)/M-phase cells. The non-invasive analysis of live cell cycle dynamics with Raman micro-spectroscopy demonstrates the potential of this approach to monitoring biochemical cellular reactions and processes in live cells in the absence of fixatives or labels.
机译:拉曼光谱是一种基于激光的技术,无需标记,标记或染色剂即可对细胞和组织进行快速,无创的​​生化分析。使用拉曼显微光谱法对哺乳动物细胞周期的先前表征包括对活细胞和单个固定和/或干燥细胞的悬浮液的分析。细胞悬浮液不提供特定于细胞的信息,固定/干燥可能会引入伪像,从而使拉曼光谱失真,从而可能使定性和定量分析结果模糊不清。在本文中,我们介绍了与体外单个活细胞内细胞周期动力学有关的生化变化的拉曼光谱表征。获得了在细胞周期的G(0)/ G(1),S和G(2)/ M期同步的人类骨肉瘤细胞的拉曼光谱,并应用多元统计数据来分析细胞光谱随细胞变化的变化循环阶段。主成分分析确定了不同阶段细胞之间的光谱差异,表明相对细胞脂质对拉曼光谱特征的贡献从G(0)/ G(1)降至G(2)/ M,同时信号相对增加核酸和蛋白质。光谱的监督线性判别分析用于根据细胞周期阶段对细胞进行分类,并显示G(0)/ G(1)相细胞和G(2)/ M相细胞之间的区分度为97%。用拉曼光谱对活细胞周期动力学进行的非侵入性分析表明,在没有固定剂或标记物的情况下,这种方法在活细胞中监测生化细胞反应和过程的潜力。

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