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通过流式细胞术分析细胞DNA含量

Analysis of Cellular DNA Content by Flow Cytometry.

作者信息

Darzynkiewicz Zbigniew, Huang Xuan, Zhao Hong

机构信息

Department of Pathology and Brander Cancer Research Institute, New York Medical College, Valhalla, New York.

Hematology/Oncology, Case Western Reserve University Cleveland, Ohio.

出版信息

Curr Protoc Cytom. 2017 Oct 2;82:7.5.1-7.5.20. doi: 10.1002/cpcy.28.

Abstract

Cellular DNA content can be measured by flow cytometry with the aim of : (1) revealing cell distribution within the major phases of the cell cycle, (2) estimating frequency of apoptotic cells with fractional DNA content, and/or (3) disclosing 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/or proteolytic treatment to permeabilize cells and make DNA accessible to fluorochrome. Additionally, supravital cell staining with Hoechst 33342, which is primarily used for sorting live cells based on DNA-content differences for their subsequent culturing, is described. Also presented are methods for staining cell nuclei isolated from paraffin-embedded tissues. Available algorithms are listed for deconvolution of DNA-content-frequency histograms to estimate percentage of cells in major phases of the cell cycle and frequency of apoptotic cells with fractional DNA content. © 2017 by John Wiley & Sons, Inc.

摘要

细胞DNA含量可通过流式细胞术进行测量,目的如下:(1) 揭示细胞在细胞周期主要阶段的分布情况;(2) 利用DNA含量分数估计凋亡细胞的频率;和/或(3) 揭示被测细胞群体的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/或蛋白水解处理使细胞通透并使DNA能够被荧光染料染色的方法。此外,还描述了用Hoechst 33342进行的超活细胞染色,该方法主要用于根据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。列出了可用的算法,用于对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。© 2017约翰威立父子出版公司

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