Ishikawa Mayuko, Ogihara Yusuke, Miura Masahiko
Oral Radiation Oncology, Department of Oral Restitution, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Biochem Biophys Res Commun. 2009 Nov 20;389(3):426-30. doi: 10.1016/j.bbrc.2009.08.160. Epub 2009 Sep 2.
Ionizing radiation (IR) influences cell cycle-associated events in tumor cells. We expressed the fusion protein of Azami Green (AG) and the destruction box plus nuclear localization signal of human Geminin, an inhibitor of DNA replication licensing factor, in oral tumor cells. This approach allowed us to visualize G2 arrest in living cells following irradiation. The combination of time-lapse imaging analysis allowed us to observe the nuclear envelope break down (NEBD) at early M phase, and disappearance of fluorescence (DF) at the end of M phase. The duration from NEBD to DF was not much affected in irradiated cells; however, most of daughter cells harbored double-strand breaks. Complete DF was also observed in cells exhibiting abnormal mitosis or cytokinesis. We conclude that the fluorescent Geminin probe could function as a stable cell cycle indicator irrespective of genome integrity.
电离辐射(IR)会影响肿瘤细胞中与细胞周期相关的事件。我们在口腔肿瘤细胞中表达了Azami Green(AG)与人类Geminin的破坏盒加核定位信号的融合蛋白,Geminin是一种DNA复制许可因子的抑制剂。这种方法使我们能够在照射后可视化活细胞中的G2期阻滞。延时成像分析相结合使我们能够观察到早期M期的核膜破裂(NEBD)以及M期末期荧光消失(DF)。照射后的细胞中从NEBD到DF的持续时间受影响不大;然而,大多数子细胞都存在双链断裂。在表现出异常有丝分裂或胞质分裂的细胞中也观察到了完全的DF。我们得出结论,荧光Geminin探针可作为一种稳定的细胞周期指示剂,而与基因组完整性无关。