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A microscopy-based small molecule screen in primary neurons reveals neuroprotective properties of the FDA-approved anti-viral drug Elvitegravir

机译:原发性神经元的基于显微镜的小分子筛网揭示了FDA批准的抗病毒药物ElviteGravir的神经保护性能

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摘要

Development of a screening assay using primary neurons. a Schematic representation of the workflow. b Example images illustrating data analysis with CellProfiler (segmentation) and CellProfiler Analyst (training and classification). Dead neurons can be identified based on their shrunken and brightly stained nuclei. c Heatmap illustrating the variability of neuronal viability between technical replicate wells. Z-scores (the number of standard deviations by which each value differs from the mean) were calculated independently for control and NMDA-treated wells. d Comparison of cell viability values that were either calculated for each single well of the plate shown in c, or based on the summed cell counts from groups of two, three, or five wells from that plate. Error bars indicate the SD
机译:使用原发性神经元进行筛选测定。工作流程的示意图。 b示例图像通过CellProfiler(分段)和CellProfiler分析师(培训和分类)说明数据分析。可以基于它们的缩小和染色的核来鉴定死神经元。 C热线图说明了技术复制孔之间神经元存量的可变性。 Z分数(每个值与平均值不同的标准偏差的数量)独立计算对照和NMDA处理的孔。 d比较C的每个单个孔的单个孔的细胞活力值,或者基于来自该板的两组,三个或五个孔的汇总细胞计数。错误栏表示SD

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