Yoshida M, Hosoi Y, Miyachi H, Ishii N, Matsumoto Y, Enomoto A, Nakagawa K, Yamada S, Suzuki N, Ono T
Departments of Radiation Research and Radiology, Tohoku University School of Medicine, Sendai, Japan.
Int J Radiat Biol. 2002 Jun;78(6):503-12. doi: 10.1080/095530002317577321.
The roles of DNA-dependent protein kinase (DNA-PK) and ATM in the cell-cycle-dependent radiosensitivity in human cells were investigated.
A DNA-PK activity-deficient human glioblastoma cell line M059J, ataxia telangiectasia cell lines AT3BISV and AT5BIVA, and control cell lines were used. Wortmannin inhibited DNA-PK and ATM activities. Cells were synchronized by hydroxyurea. Progression through the cell cycle was analysed by flow cytometry.
M059J exhibited hyper-radiosensitivity throughout the cell cycle, with extreme hyper-radiosensitivity in G to early S-phase compared with the control cell line M059K. AT3BISV and AT5BIVA exhibited hyper-radiosensitivity throughout the cell cycle but showed a similar pattern of cell-cycle-dependent radiosensitivity to that observed in LM217 or HeLa cells. In AT3BISV and AT5BIVA, radiosensitization by wortmannin was observed throughout the cell cycle and was most prominent in G1 to early S-phase. Wortmannin did not sensitize M059J to ionizing radiation in any cell-cycle phase. DNA-PK activities were not different throughout the cell cycle.
The results suggest that (1) non-homologous endjoining plays a dominant role in G1 to early S-phase and a minor role in late S to G2-phase in repairing DNA double-strand breaks, (2) the role of ATM in repairing double-strand breaks may be almost cell-cycle-independent and (3) the dominant role of non-homologous end-joining during G1 to early S-phase is not due to cell-cycle-dependent fluctuations in DNA-PK activity.
研究DNA依赖性蛋白激酶(DNA-PK)和ATM在人类细胞周期依赖性放射敏感性中的作用。
使用DNA-PK活性缺陷的人胶质母细胞瘤细胞系M059J、共济失调毛细血管扩张症细胞系AT3BISV和AT5BIVA以及对照细胞系。渥曼青霉素抑制DNA-PK和ATM活性。细胞用羟基脲同步化。通过流式细胞术分析细胞周期进程。
与对照细胞系M059K相比,M059J在整个细胞周期中表现出高放射敏感性,在G期到早S期具有极高的放射敏感性。AT3BISV和AT5BIVA在整个细胞周期中表现出高放射敏感性,但显示出与LM217或HeLa细胞中观察到的类似的细胞周期依赖性放射敏感性模式。在AT3BISV和AT5BIVA中,渥曼青霉素在整个细胞周期中均观察到放射增敏作用,在G1期到早S期最为显著。渥曼青霉素在任何细胞周期阶段均未使M059J对电离辐射敏感。DNA-PK活性在整个细胞周期中无差异。
结果表明:(1)非同源末端连接在修复DNA双链断裂中在G1期到早S期起主导作用,在晚S期到G2期起次要作用;(2)ATM在修复双链断裂中的作用可能几乎与细胞周期无关;(3)G1期到早S期非同源末端连接的主导作用并非由于DNA-PK活性的细胞周期依赖性波动。