Comparative Analysis of the Formation of γH2AX Foci in Human Mesenchymal Stem Cells Exposed to 3H-Thymidine, Tritium Oxide, and X-Rays Irradiation

We performed a comparative study of the formation of γН2АХ foci (a marker of DNA doublestrand breaks) in human bone marrow mesenchymal stem cells after 24-h incubation with 3 Н-thimidin and tritium oxide with low specific activities (50-800 MBq/liter). The dependence of the number of γH2AX foci on s...

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Published in:Bulletin of experimental biology and medicine Vol. 166; no. 1; pp. 178 - 181
Main Authors: Vorob’eva, N. Yu, Kochetkov, O. A., Pustovalova, M. V., Grekhova, A. K., Blokhina, T. M., Yashkina, E. I., Osipov, A. A., Kabanov, D. I., Surin, P. P., Barchukov, V. G., Osipov, A. N.
Format: Journal Article
Language:English
Published: New York Springer US 01-11-2018
Springer Nature B.V
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Summary:We performed a comparative study of the formation of γН2АХ foci (a marker of DNA doublestrand breaks) in human bone marrow mesenchymal stem cells after 24-h incubation with 3 Н-thimidin and tritium oxide with low specific activities (50-800 MBq/liter). The dependence of the number of γH2AX foci on specific activity of 3H-thymidine was described by a linear equation y =2.21+43.45 x ( R 2 =0.96), where y is the number of γH2AX foci per nucleus and x is specific activity in 1000 MBq/liter. For tritium oxide, the relationship was described by a linear equation y =2.52+6.70 x ( R 2 =0.97). Thus, the yield of DNA double-strand breaks after exposure to 3 H-thymidine was 6.5-fold higher than after exposure to tritium oxide. Comparison of the effects of tritium oxide and X-ray radiation on the yield of DNA double-strand breaks showed that the relative biological efficiency of tritium oxide in a dose range of 3.78-60.26 mGy was 1.6-fold higher than that of X-ray radiation. Improvement of the methods of analysis of DNA double-strand breaks repair foci is highly promising in the context of creation of highly sensitive biodosimetry technologies for tritium compounds in humans.
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ISSN:0007-4888
1573-8221
DOI:10.1007/s10517-018-4309-1