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Radiation-Induced Elevation of Plasma DNA in Mice is Associated with Genomic Background

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Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 737))

Abstract

Genomic background helps determine sensitivity to TBI. Since the LD50/30 (the dose that causes death in half of exposed mice within 30 days) following TBI varies between murine strains, we tested four murine strains to determine whether TBI sensitivity was associated with different levels of circulating DNA after radiation. The LD50/30 for the mice we tested – BALB/c, NIH Swiss, C3H/HeN, and C57BL/6 – is approximately 5.8 ± 0.3, 7.3 ± 0.2, 7.4 ± 0.3, and 8.5 ± 0.3 Gy, respectively. We estimated the radiation dose at which circulating DNA reached a peak level (peakGy), and mice were subjected to different doses at 1.84 Gy/min. The peakGy was 6, 7, 9, and 9 Gy for BALB/c, NIH Swiss, C3H/HeN, and C57BL/6, which corresponds to each strain’s respective LD50/30. BALB/c, the most sensitive strain, had the lowest DNA concentration at peakGy, while C57BL/6, the most resistant strain, had the highest concentration at peakGy. At 7 Gy, the plasma DNA was approximately 3,754 ± 636, 8,238 ± 2,704, 9,773 ± 2,821, and 22,733 ± 5,914 ng/ml for BALB/c, NIH Swiss, C3H/HeN, and C57BL/6, respectively. These findings support our hypothesis that plasma DNA level is associated with genomic background.

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Reference

  1. Zhang L, Zhang M, Yang S et al (2010) A new biodosimetric method: branched DNA-based quantitative detection of B1 DNA in mouse plasma. Br J Radiol 83:694–701

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Acknowledgments

The authors gratefully acknowledge the funding of this work in part by a grant (U19-AI067733) from the National Institute of Allergy and Infectious Diseases (NIAID) and a STTR from DARPA (W31P4Q08C0417).

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Correspondence to Paul Okunieff M.D. .

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© 2012 Springer Science+Business Media, LLC

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Zhang, L. et al. (2012). Radiation-Induced Elevation of Plasma DNA in Mice is Associated with Genomic Background. In: Wolf, M., et al. Oxygen Transport to Tissue XXXIII. Advances in Experimental Medicine and Biology, vol 737. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-1566-4_22

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