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首页> 外文期刊>Biochemical and Biophysical Research Communications >Unusual expression of red fluorescence at M phase induced by anti-microtubule agents in HeLa cells expressing the fluorescent ubiquitination-based cell cycle indicator (Fucci)
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Unusual expression of red fluorescence at M phase induced by anti-microtubule agents in HeLa cells expressing the fluorescent ubiquitination-based cell cycle indicator (Fucci)

机译:抗微管剂在HeLa细胞中表达基于泛素化的细胞周期指示剂(Fucci)的M期红色荧光的异常表达

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Plinabulin (NPI-2358) is a novel microtubule-depolymerizing agent. In HeLa cells, plinabulin arrests the cell-cycle at M phase and subsequently induces mitotic catastrophe. To better understand the effects on this compound on the cell-cycle, we used the fluorescent ubiquitination-based cell cycle indicator (Fucci), which normally enables G1 and S/G2/M cells to emit red and green fluorescence, respectively. When HeLa-Fucci cells were treated with 50. nM plinabulin, cells began to fluoresce both green and red in an unusual pattern; most cells exhibited the new pattern after 24. h of treatment. X-irradiation efficiently induced G2 arrest in plinabulin-treated cells and significantly retarded the emergence of the unusual pattern, suggesting that entering M phase is essential for induction of the pattern. By simultaneously visualizing chromosomes with GFP-histone H2B, we established that the pattern emerges after nuclear envelope breakdown but before metaphase. Pedigree assay revealed a significant relationship between the unusual expression and mitotic catastrophe. Nocodazole, KPU-133 (a more potent derivative of plinabulin), and paclitaxel also exerted similar effects. From these data, we conclude that the unusual pattern may be associated with dysregulation of late M phase-specific E3 ligase activity and mitotic catastrophe following treatment with anti-microtubule agents.
机译:Plinabulin(NPI-2358)是一种新型的微管解聚剂。在HeLa细胞中,纤毛蛋白将细胞周期停滞在M期,随后诱发有丝分裂灾难。为了更好地了解此化合物对细胞周期的影响,我们使用了基于荧光泛素化的细胞周期指示剂(Fucci),该指示剂通常可使G1和S / G2 / M细胞分别发出红色和绿色荧光。当用50nM纤溶蛋白处理HeLa-Fucci细胞时,细胞开始以不寻常的模式发出绿色和红色荧光。在处理24小时后,大多数细胞表现出新的模式。 X射线辐射有效地诱导了纤连蛋白处理的细胞中的G2阻滞,并显着抑制了异常模式的出现,这表明进入M期对于诱导模式至关重要。通过同时可视化与GFP组蛋白H2B的染色体,我们确定该模式出现在核被膜破裂后但进入中期。家谱分析揭示了异常表达与有丝分裂灾难之间的显着关系。诺考达唑,KPU-133(匹拉布林的更有效衍生物)和紫杉醇也发挥了类似的作用。根据这些数据,我们得出结论,这种异常模式可能与使用抗微管剂治疗的晚期M期特异性E3连接酶活性失调和有丝分裂灾难有关。

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