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| Hauptseite > Publikationsdatenbank > Genotoxicity of the Auger electron emitter I-123-iododeoxyuridine in vitro > print |
| Hauptseite > Publikationsdatenbank > Genotoxicity of the Auger electron emitter I-123-iododeoxyuridine in vitro > print |
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| 100 | 1 | _ | |a Unverricht, Marcus |0 P:(DE-Juel1)133466 |b 0 |e Corresponding author |u fzj |
| 111 | 2 | _ | |a 38th Annual Meeting of the European Radiation Research Society |g ERRS |c Stockholm |d 2010-09-05 - 2010-09-09 |w Sweden |
| 245 | _ | _ | |a Genotoxicity of the Auger electron emitter I-123-iododeoxyuridine in vitro |
| 260 | _ | _ | |c 2010 |
| 336 | 7 | _ | |a Conference Paper |0 33 |2 EndNote |
| 336 | 7 | _ | |a INPROCEEDINGS |2 BibTeX |
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| 520 | _ | _ | |a OBJECTIVES: The biological effectiveness of Auger electron emitters (AEE) is attributed to the numerous short-range electrons released during the decay of the radionuclide. Damage on cellular level depends largely on the intracellular distribution of the radionuclides. AEE located exclusively in the cytoplasm produce low-LET type cell survival curves, whereas DNA-associated AEE cause high-LET type survival curves. To determine whether AEE induce high-LET type genotoxic effects micronucleus induction and γ-H2AX formation were analyzed after exposure to I-123-iododeoxyuridine (I-123-UdR) in comparison to high- and low-LET radiation.MATERIALS AND METHODS: Human T-lymphoma Jurkat cells were either exposed to I-123-UdR (0.5-50 kBq/ml) for 20 h or irradiated with different doses of low-LET Cs-137 γ-rays or high-LET Am-241 α-particles. Cells were assayed for micronucleus formation (Cytochalasin B assay) employing automated image analysis (MetaSystems, Germany). The γ-H2AX foci were quantified by measuring the mean signal intensity of γ-H2AX foci per cell using flow cytometry and by counting the number of γ-H2AX foci with a fluorescence microscope.RESULTS: In contrast to γ- and α-irradiation the numbers of γ-H2AX foci per cell showed a much more pronounced increase after exposure to I-123-UdR. However, the mean intensity of γ H2AX signals per cell, as measured by flow cytometry, was very similar for exposure to I-123-UdR and α-particles. Single γ H2AX foci induced by I-123-UdR appear to be smaller and/or less intense stained than those after α-irradiation and resemble γ H2AX foci induced by γ-rays. Micronucleus induction was almost identical for all three investigated radiation qualities.CONCLUSIONS: I-123-UdR is a very potent inducer of γ H2AX foci in comparison to γ- and α-radiation. Taken into account the very low dose rate of I-123-UdR exposure the effect is even more pronounced. Micronucleus induction does not depend on radiation quality in Jurkat cells.Supported by the Federal Ministry of Education and Research, BMBF |
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