Allen P D, Newland A C
Department of Haematology, St. Bartholomew's and the Royal London Hospital School of Medicine and Dentistry, Whitechapel, London.
Mol Biotechnol. 1998 Jun;9(3):247-51. doi: 10.1007/BF02915798.
There are many techniques available for the detection of apoptotic cells; some are based on morphological changes, others on biochemical events. However, electrophoretic detection of the systematic cleavage of DNA into oligonucleosomal multimers of 180-200 bp remains the "hallmark" of apoptosis. Conventional constant field agarose gel electrophoresis of DNA from apoptotic cells can be used to resolve the multimers into the characteristic DNA ladders indicative of apoptotic cell death. More recently, it has become clear that the generation of the lower molecular weight oligonucleosomal DNA is preceded by the generation of higher molecular weight fragments. In some cell types, DNA cleavage proceeds no further than the formation of 300 and/or 50 kbp cleavage products. DNA fragmentation of this size can only be resolved using a form of pulsed-field gel electrophoresis. Basic "starter" protocols for conventional and pulsed field electrophoresis for the detection of apoptotic cell DNA are described in this article.
有许多技术可用于检测凋亡细胞;一些基于形态学变化,另一些基于生化事件。然而,通过电泳检测DNA系统切割成180 - 200 bp的寡核小体多聚体仍然是凋亡的“标志”。凋亡细胞DNA的常规恒定电场琼脂糖凝胶电泳可用于将多聚体解析为指示凋亡细胞死亡的特征性DNA梯带。最近,已经清楚的是,较低分子量寡核小体DNA的产生之前会先产生较高分子量的片段。在某些细胞类型中,DNA切割仅进行到形成300和/或50 kbp切割产物的程度。这种大小的DNA片段化只能使用一种脉冲场凝胶电泳形式来解析。本文描述了用于检测凋亡细胞DNA的常规和脉冲场电泳的基本“入门”方案。