Irradiation of mammalian cultured cells with a collimated heavy-ion microbeam

被引:32
作者
Funayama, T [1 ]
Wada, S [1 ]
Kobayashi, Y [1 ]
Watanabe, H [1 ]
机构
[1] JAERI Takasaki, Res Grp Biotechnol Dev, Takasaki, Gumma 3701292, Japan
关键词
D O I
10.1667/RR3301
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
As the first step for the analysis of the biological effect of heavy charged-particle radiation, we established a method for the irradiation of individual cells with a heavy-ion microbeam apparatus at JAERI-Takasaki. CHO-K1 cells attached on a thin film of an ion track detector, CR-39, were automatically detected under a fluorescence microscope and irradiated individually with an Ar-40(13+) ion (11.5 MeV/nucleon, LET 1260 keV/mum) microbeam. Without killing the irradiated cells, trajectories of irradiated ions were visualized as etch pits by treatment of the CR-39 with an alkaline-ethanol solution at 37degreesC. The exact positions of ion hits were determined by overlaying images of both cells and etch pits. The cells that were irradiated with argon ions showed a reduced growth in postirradiation observations. Moreover, a single hit of an argon ion to the cell nucleus resulted in strong growth inhibition. These results tell us that our verified irradiation method enables us to start a precise study of the effects of high-LET radiation on cells. (C) 2005 by Radiation Research Society.
引用
收藏
页码:241 / 246
页数:6
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