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Biological studies using mammalian cell lines and the current status of the microbeam irradiation system,SPICE
Authors:T. Konishi  T. Ishikawa  H. Iso  N. Yasuda  M. Oikawa  Y. Higuchi  T. Kato  K. Hafer  K. Kodama  T. Hamano  N. Suya  H. Imaseki
Affiliation:1. Dept. of Technical Support and Development, Fundamental Technology Center, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba 263-8555, Japan;2. Neos-Tech Co. Ltd., Benten 4-11-13-202, Chuo-ku, Chiba 206-0045, Japan;3. Graduate School of Science, Rikkyo University, 3-34-1 Nishi-Ikebukuro, Toshimaku, Tokyo 171-8501, Japan;4. Department of Radiation Oncology, UCLA School of Medicine, Los Angeles, CA, USA
Abstract:The development of SPICE (single-particle irradiation system to cell), a microbeam irradiation system, has been completed at the National Institute of Radiological Sciences (NIRS). The beam size has been improved to approximately 5 μm in diameter, and the cell targeting system can irradiate up to 400–500 cells per minute. Two cell dishes have been specially designed: one a Si3N4 plate (2.5 mm × 2.5 mm area with 1 μm thickness) supported by a 7.5 mm × 7.5 mm frame of 200 μm thickness, and the other a Mylar film stretched by pressing with a metal ring. Both dish types may be placed on a voice coil stage equipped on the cell targeting system, which includes a fluorescent microscope and a CCD camera for capturing cell images. This microscope system captures images of dyed cell nuclei, computes the location coordinates of individual cells, and synchronizes this with the voice coil motor stage and single-particle irradiation system consisting of a scintillation counter and a beam deflector. Irradiation of selected cells with a programmable number of protons is now automatable. We employed the simultaneous detection method for visualizing the position of mammalian cells and proton traversal through CR-39 to determine whether the targeted cells are actually irradiated. An immuno-assay was also performed against γ-H2AX, to confirm the induction of DNA double-strand breaks in the target cells.
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