Darzynkiewicz Zbigniew, Huang Xuan
New York Medical Center, Valhalla, New York, USA.
Curr Protoc Immunol. 2004 May;Chapter 5:Unit 5.7. doi: 10.1002/0471142735.im0507s60.
Cellular DNA content can be measured by flow or laser-scanning cytometry with the aim of (1) revealing cell distribution within the major phases of the cell cycle, (2) estimating the frequency of apoptotic cells with fractional DNA content, and/or (3) disclosing the DNA-ploidy of the measured cell population. In this unit, simple and universally applicable methods for staining fixed cells are presented, as are methods that utilize detergents and proteolytic treatment to permeabilize cells. Additionally, supravital cell staining with Hoechst 33342, which is primarily used for sorting live cells for subsequent culturing based on DNA-content differences, is also described. Also presented are methods for staining of cell nuclei isolated from paraffin-embedded tissues, and deconvolution of DNA-content-frequency histograms to estimate the percentage of cells in major phases of the cell cycle and frequency of apoptotic cells with fractional DNA content.
细胞DNA含量可通过流式细胞术或激光扫描细胞术进行测量,目的在于:(1)揭示细胞在细胞周期主要阶段的分布情况;(2)通过DNA含量分数估计凋亡细胞的频率;和/或(3)揭示所测细胞群体的DNA倍性。在本单元中,介绍了用于固定细胞染色的简单且普遍适用的方法,以及利用去污剂和蛋白水解处理使细胞通透的方法。此外,还描述了用Hoechst 33342进行的超活细胞染色,该染色主要用于根据DNA含量差异对活细胞进行分选以便后续培养。还介绍了从石蜡包埋组织中分离细胞核的染色方法,以及对DNA含量频率直方图进行反卷积以估计细胞周期主要阶段的细胞百分比和具有分数DNA含量的凋亡细胞频率的方法。