Center for Computational Toxicology and Exposure (CCTE), Office of Research and Development, U.S. Environmental Protection Agency, Durham, NC, USA.
Oak Ridge Associated Universities (ORAU), Oak Ridge, TN, USA.
SLAS Discov. 2020 Aug;25(7):755-769. doi: 10.1177/2472555220928004. Epub 2020 Jun 17.
Cell Painting is a high-throughput phenotypic profiling assay that uses fluorescent cytochemistry to visualize a variety of organelles and high-content imaging to derive a large number of morphological features at the single-cell level. Most Cell Painting studies have used the U-2 OS cell line for chemical or functional genomics screening. The Cell Painting assay can be used with many other human-derived cell types, given that the assay is based on the use of fluoroprobes that label organelles that are present in most (if not all) human cells. Questions remain, however, regarding the optimization steps required and overall ease of deployment of the Cell Painting assay to novel cell types. Here, we used the Cell Painting assay to characterize the phenotypic effects of 14 phenotypic reference chemicals in concentration-response screening mode across six biologically diverse human-derived cell lines (U-2 OS, MCF7, HepG2, A549, HTB-9 and ARPE-19). All cell lines were labeled using the same cytochemistry protocol, and the same set of phenotypic features was calculated. We found it necessary to optimize image acquisition settings and cell segmentation parameters for each cell type, but did not adjust the cytochemistry protocol. For some reference chemicals, similar subsets of phenotypic features corresponding to a particular organelle were associated with the highest-effect magnitudes in each affected cell type. Overall, for certain chemicals, the Cell Painting assay yielded qualitatively similar biological activity profiles among a group of diverse, morphologically distinct human-derived cell lines without the requirement for cell type-specific optimization of cytochemistry protocols.
细胞画像是一种高通量表型分析检测方法,它利用荧光细胞化学技术来可视化各种细胞器,并利用高内涵成像技术在单细胞水平上获得大量形态特征。大多数细胞画谱研究都使用 U-2 OS 细胞系进行化学或功能基因组筛选。细胞画谱检测可以用于许多其他源自人类的细胞类型,因为该检测方法基于使用荧光探针标记存在于大多数(如果不是全部)人类细胞中的细胞器。然而,对于需要优化的步骤以及将细胞画谱检测方法应用于新型细胞类型的总体易用性,仍然存在一些问题。在这里,我们使用细胞画谱检测方法在浓度反应筛选模式下,在六个具有不同生物学特性的人类衍生细胞系(U-2 OS、MCF7、HepG2、A549、HTB-9 和 ARPE-19)中,对 14 种表型参考化学物质的表型效应进行了特征描述。所有细胞系均使用相同的细胞化学方案进行标记,并计算了相同的表型特征集。我们发现有必要针对每种细胞类型优化图像采集设置和细胞分割参数,但无需调整细胞化学方案。对于某些参考化学物质,与特定细胞器相对应的类似表型特征子集与受影响的每种细胞类型中的最高效应幅度相关。总体而言,对于某些化学物质,细胞画谱检测方法在一组形态不同的多样化人类衍生细胞系中产生了定性相似的生物学活性谱,而无需针对细胞化学方案进行特定于细胞类型的优化。