Sherman Sean P, Alva Jackelyn A, Thakore-Shah Kaushali, Pyle April D
Lab of Dr. April D. Pyle, Molecular Biology Institute, University of California, Los Angeles, Los Angeles, CA, USA.
Methods Mol Biol. 2011;767:283-95. doi: 10.1007/978-1-61779-201-4_21.
High-content screening (HCS) permits simultaneous observation and analysis of multiple cellular variables including cell morphology, survival, and differentiation in live cells at the single-cell level, at the level of the culture well, and across the entire culture. By combining high-throughput technologies such as robotics, chemical libraries, and automated high-resolution microscopy, scientists are able to evaluate a much broader array of experimental conditions than can be studied using conventional cell biological techniques that study fewer parameters at any one time. Thus, HCS assays provide a means to vastly improve our basic understanding of stem cell biology. We have developed a HCS assay that allows the study of the effects of hundreds of small molecules in parallel. The protocol described in this chapter was developed to assess the effects of small molecules on the survival, proliferation, and expression of pluripotent markers following single-cell dissociation of human embryonic stem cells, but can be applied to the study of other types of stem cells including induced pluripotent stem cells. A detailed protocol for the setup of HCS assays and the parameters used to identify chemical modifiers of survival in human pluripotent stem cells, as well as secondary assays used to validate the small-molecule "hits" obtained during the high-content screen, are described.
高内涵筛选(HCS)允许在单细胞水平、培养孔水平以及整个培养体系中同时观察和分析多个细胞变量,包括活细胞中的细胞形态、存活和分化情况。通过结合机器人技术、化学文库和自动化高分辨率显微镜等高通量技术,科学家能够评估比使用传统细胞生物学技术更广泛的一系列实验条件,传统细胞生物学技术在任何时候研究的参数都较少。因此,HCS分析为极大地增进我们对干细胞生物学的基本理解提供了一种手段。我们开发了一种HCS分析方法,可同时研究数百种小分子的作用。本章所述方案旨在评估小分子对人胚胎干细胞单细胞解离后存活、增殖和多能性标志物表达的影响,但也可应用于包括诱导多能干细胞在内的其他类型干细胞的研究。文中描述了HCS分析设置的详细方案、用于鉴定人多能干细胞存活化学调节剂的参数,以及用于验证在高内涵筛选中获得的小分子“命中物”的二次分析方法。