Suppr超能文献

基于微核频率评估细胞周期中 HeLa 细胞放射敏感性的波动。

Fluctuation in radioresponse of HeLa cells during the cell cycle evaluated based on micronucleus frequency.

机构信息

Division of Oral Health Sciences, Department of Oral Radiation Oncology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8549, Japan.

Division of Oral Health Sciences, Department of Oral and Maxillofacial Surgery, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8549, Japan.

出版信息

Sci Rep. 2020 Nov 30;10(1):20873. doi: 10.1038/s41598-020-77969-0.

Abstract

In this study, we examined the fluctuation in radioresponse of HeLa cells during the cell cycle. For this purpose, we used HeLa cells expressing two types of fluorescent ubiquitination-based cell cycle indicators (Fucci), HeLa-Fucci (CA)2 and HeLa-Fucci (SA), and combined this approach with the micronucleus (MN) assay to assess radioresponse. The Fucci system distinguishes cell cycle phases based on the colour of fluorescence and cell morphology under live conditions. Time-lapse imaging allowed us to further identify sub-positions within the G1 and S phases at the time of irradiation by two independent means, and to quantitate the number of MNs by following each cell through M phase until the next G1 phase. Notably, we found that radioresponse was low in late G1 phase, but rapidly increased in early S phase. It then decreased until late S phase and increased in G2 phase. For the first time, we demonstrated the unique fluctuation of radioresponse by the MN assay during the cell cycle in HeLa cells. We discuss the difference between previous clonogenic experiments using M phase-synchronised cell populations and ours, as well as the clinical implications of the present findings.

摘要

在这项研究中,我们研究了 HeLa 细胞在细胞周期中放射反应的波动。为此,我们使用表达两种荧光泛素化细胞周期指示剂(Fucci)的 HeLa 细胞,即 HeLa-Fucci(CA)2 和 HeLa-Fucci(SA),并将这种方法与微核(MN)测定相结合,以评估放射反应。Fucci 系统基于荧光颜色和活细胞条件下的细胞形态来区分细胞周期阶段。延时成像使我们能够通过两种独立的方法进一步识别照射时 G1 和 S 期的亚位置,并通过跟踪每个细胞穿过 M 期直到下一个 G1 期来定量 MN 的数量。值得注意的是,我们发现晚期 G1 期的放射反应较低,但在早期 S 期迅速增加。然后,它在晚期 S 期下降,并在 G2 期增加。我们首次通过 MN 测定法在 HeLa 细胞的细胞周期中证明了放射反应的独特波动。我们讨论了我们与之前使用 M 期同步化细胞群体进行的克隆形成实验之间的差异,以及本研究结果的临床意义。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验