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Time-Resolved Study of Nanoparticle Induced Apoptosis Using Microfabricated Single Cell Arrays

机译:时间分辨研究的纳米粒子诱导的细胞凋亡使用微制造的单细胞阵列。

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摘要

Cell fate decisions like apoptosis are heterogeneously implemented within a cell population and, consequently, the population response is recognized as sum of many individual dynamic events. Here, we report on the use of micro-patterned single-cell arrays for real-time tracking of nanoparticle-induced (NP) cell death in sets of thousands of cells in parallel. Annexin (pSIVA) and propidium iodide (PI), two fluorescent indicators of apoptosis, are simultaneously monitored after exposure to functionalized polystyrene (PS − NH2) nanobeads as a model system. We find that the distribution of Annexin onset times shifts to later times and broadens as a function of decreasing NP dose. We discuss the mean time-to-death as a function of dose, and show how the EC50 value depends both on dose and time of measurement. In addition, the correlations between the early and late apoptotic markers indicate a systematic shift from apoptotic towards necrotic cell death during the course of the experiment. Thus, our work demonstrates the potential of array-based single cell cytometry for kinetic analysis of signaling cascades in a high-throughput format.
机译:诸如凋亡等细胞命运决定是在细胞群体中异质实现的,因此,群体响应被认为是许多个体动态事件的总和。在这里,我们报告使用微模式的单细胞阵列实时跟踪并行的成千上万的细胞中的纳米粒子诱导(NP)细胞死亡。暴露于功能化聚苯乙烯(PS-NH2)纳米珠作为模型系统后,膜联蛋白(pSIVA)和碘化丙啶(PI)是细胞凋亡的两个荧光指示剂,同时进行监测。我们发现,膜联蛋白起效时间的分布转移到较晚的时间,并随着NP剂量的减少而变宽。我们讨论了平均死亡时间与剂量的关系,并显示EC50值如何取决于剂量和测量时间。另外,早期和晚期凋亡标记之间的相关性表明在实验过程中从凋亡向坏死细胞的系统转移。因此,我们的工作证明了以阵列为基础的单细胞细胞计数技术以高通量格式对信号级联反应进行动力学分析的潜力。

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