Université François-Rabelais de Tours, Tours, France.
PLoS One. 2013 Jul 30;8(7):e68425. doi: 10.1371/journal.pone.0068425. Print 2013.
An optimal technology for cell cycle analysis would allow the concomitant measurement of apoptosis, G0, G1, S, G2 and M phases in combination with cell surface phenotyping. We have developed an easy method in flow cytometry allowing this discrimination in an only two-color fluorescent plot. It is based on the concomitant use of 7-amino-actinomycin D and the antibodies anti-Ki67 and anti-phospho(Ser10)-histone H3, both conjugated to Alexa Fluor®488 to discriminate G0 and M phases, respectively. The method is particularly valuable in a clinical setting as verified in our laboratory by analyzing human leukemic cells from marrow samples or after exposure to cell cycle modifiers.
一种理想的细胞周期分析技术应该能够同时测量细胞凋亡、G0、G1、S、G2 和 M 期,并结合细胞表面表型进行分析。我们已经开发了一种简单的流式细胞术方法,可以在仅使用两种荧光标记的二维散点图中实现这种区分。该方法基于同时使用 7-氨基放线菌素 D 和抗 Ki67 抗体及磷酸化组蛋白 H3(Ser10)抗体(均与 Alexa Fluor®488 偶联)来分别区分 G0 和 M 期。该方法在临床环境中特别有价值,我们通过分析骨髓样本中的人类白血病细胞或在接触细胞周期调节剂后在实验室中进行了验证。