Wållberg Fredrik, Tenev Tencho, Meier Pascal
Chester Beatty Laboratories, The Breakthrough Toby Robins Breast Cancer Research Centre, Institute of Cancer Research, London, UK.
Methods Mol Biol. 2013;1004:17-29. doi: 10.1007/978-1-62703-383-1_2.
The processes of dying are as tightly regulated as those of growth and proliferation. Recent work into the molecular pathways that regulate and execute cell death have uncovered a plethora of signalling cascades that lead to distinct modes of cell death, including "apoptosis," "necrosis," "autophagic cell death," and "mitotic catastrophe." Given that cells can readily switch from one form of death to another, it is vital to carefully monitor the form of death under investigation. Particularly, end-point techniques are intrinsically unsuitable for assessing apoptosis versus necrosis, as they cannot reconstruct the sequence of events that have led to cell death. Since apoptotic cells frequently undergo secondary necrosis under in vitro culture conditions, novel methods relying on high-throughput time-lapse fluorescence video microscopy have been developed. Here we describe the use of this technique to reliably distinguish necrosis from apoptosis and secondary necrosis.
细胞死亡过程与细胞生长和增殖过程一样受到严格调控。最近对调控和执行细胞死亡的分子途径的研究发现了大量信号级联反应,这些反应导致了不同的细胞死亡模式,包括“凋亡”、“坏死”、“自噬性细胞死亡”和“有丝分裂灾难”。鉴于细胞能够轻易地从一种死亡形式转变为另一种死亡形式,仔细监测所研究的死亡形式至关重要。特别是,终点技术本质上不适用于评估凋亡与坏死,因为它们无法重建导致细胞死亡的事件序列。由于凋亡细胞在体外培养条件下经常会发生继发性坏死,因此已经开发出了依赖高通量延时荧光视频显微镜的新方法。在此,我们描述了使用该技术可靠地区分坏死与凋亡以及继发性坏死的方法。