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细胞绘画增强版:通过迭代染色-洗脱循环扩展基于细胞绘画的表型分析的多重检测能力。

Cell Painting PLUS: expanding the multiplexing capacity of Cell Painting-based phenotypic profiling using iterative staining-elution cycles.

作者信息

von Coburg Elena, Wedler Marlene, Muino Jose M, Wolff Christopher, Körber Nils, Dunst Sebastian, Liu Shu

机构信息

German Centre for the Protection of Laboratory Animals (Bf3R), German Federal Institute for Risk Assessment (BfR), Berlin, Germany.

Department of Food Chemistry, University of Potsdam, Potsdam, Germany.

出版信息

Nat Commun. 2025 Apr 24;16(1):3857. doi: 10.1038/s41467-025-58765-8.

Abstract

Phenotypic changes in the morphology and internal organization of cells can indicate perturbations in cell functions. Therefore, imaging-based high-throughput phenotypic profiling (HTPP) applications such as Cell Painting (CP) play an important role in basic and translational research, drug discovery, and regulatory toxicology. Here we present the Cell Painting PLUS (CPP) assay, an efficient, robust and broadly applicable approach that further expands the versatility of available HTPP methods and offers additional options for addressing mode-of-action specific research questions. An iterative staining-elution cycle allows multiplexing of at least seven fluorescent dyes that label nine different subcellular compartments and organelles including the plasma membrane, actin cytoskeleton, cytoplasmic RNA, nucleoli, lysosomes, nuclear DNA, endoplasmic reticulum, mitochondria, and Golgi apparatus. In this way, CPP significantly expands the flexibility, customizability, and multiplexing capacity of the original CP method and, importantly, also improves the organelle-specificity and diversity of the phenotypic profiles due to the separate imaging and analysis of single dyes in individual channels.

摘要

细胞形态和内部组织的表型变化可表明细胞功能的扰动。因此,基于成像的高通量表型分析(HTPP)应用,如细胞绘画(CP),在基础研究和转化研究、药物发现及监管毒理学中发挥着重要作用。在此,我们介绍细胞绘画增强版(CPP)分析方法,这是一种高效、稳健且广泛适用的方法,它进一步拓展了现有HTPP方法的多功能性,并为解决特定作用模式的研究问题提供了更多选择。一个迭代的染色 - 洗脱循环允许至少七种荧光染料进行多重标记,这些染料可标记九个不同的亚细胞区室和细胞器,包括质膜、肌动蛋白细胞骨架、细胞质RNA、核仁、溶酶体、核DNA、内质网、线粒体和高尔基体。通过这种方式,CPP显著扩展了原始CP方法的灵活性、可定制性和多重标记能力,重要的是,由于在各个通道中对单个染料进行单独成像和分析,它还提高了表型谱的细胞器特异性和多样性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b710/12022024/c38daf2573be/41467_2025_58765_Fig1_HTML.jpg

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