Darzynkiewicz Zbigniew
The Brander Cancer Research Institute and Department of Pathology, New York Medical Center, Valhalla, NY, USA.
Curr Protoc Cytom. 2010 Apr;Chapter 7:Unit7.2. doi: 10.1002/0471142956.cy0702s52.
This unit covers general aspects of DNA content analysis and provides introductory or complementary information to the specific protocols of DNA content assessment in this chapter. It describes principles of DNA content analysis and outlines difficulties and pitfalls common to these methods. It also reviews methods of DNA staining in live, permeabilized, and fixed cells, and in cell nuclei isolated from paraffin-embedded tissues, as well as the approaches to stain DNA concurrently with cell immunophenotype. This unit addresses factors affecting accuracy of DNA measurement, such as chromatin features restricting accessibility of fluorochromes to DNA, stoichiometry of interaction with DNA, and "mass action law" characterizing binding to DNA in relation to unbound fluorochrome concentration. It also describes controls to ensure accuracy and quality control of DNA content determination and principles of DNA ploidy assessment. Because many aspects of DNA content analysis are common to protocols in UNITS 7.3, 7.6, 7.16, 7.20, 7.23, & 7.25, certain parts of this unit provide information redundant with commentaries in these units.
本单元涵盖DNA含量分析的一般方面,并为本章中DNA含量评估的具体方案提供介绍性或补充信息。它描述了DNA含量分析的原理,并概述了这些方法常见的困难和陷阱。它还综述了在活细胞、通透细胞和固定细胞中,以及从石蜡包埋组织中分离的细胞核中进行DNA染色的方法,以及与细胞免疫表型同时对DNA进行染色的方法。本单元讨论了影响DNA测量准确性的因素,如限制荧光染料接近DNA的染色质特征、与DNA相互作用的化学计量关系,以及与未结合荧光染料浓度相关的DNA结合“质量作用定律”。它还描述了确保DNA含量测定准确性和质量控制的对照以及DNA倍性评估的原则。由于DNA含量分析的许多方面在单元7.3、7.6、7.16、7.20、7.23和7.25的方案中是共有的,因此本单元的某些部分提供了与这些单元中的注释重复的信息。