Development of hematopoietic syndrome mice model for localized radiation exposure
Abstract Current models to study the hematopoietic syndrome largely rely on the uniform whole-body exposures. However, in the radio-nuclear accidents or terrorist events, exposure can be non-uniform. The data available on the non-uniform exposures is limited. Thus, we have developed a mice model for...
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doaj-d0f3564a89ec42b6a0fd3abb5eb265782021-01-10T12:46:44ZengNature Publishing GroupScientific Reports2045-23222021-01-0111111210.1038/s41598-020-80075-wDevelopment of hematopoietic syndrome mice model for localized radiation exposureM. H. Yashavarddhan0Ajay Kumar Sharma1Pankaj Chaudhary2Sania Bajaj3Sukhvir Singh4Sandeep Kumar Shukla5National Institute of Cancer Prevention & Research, Indian Council of Medical ResearchInstitute of Nuclear Medicine and Allied Sciences, Defence Research and Development OrganisationThe Patrick G Johnston Centre for Cancer Research, Queen’s University BelfastInstitute of Nuclear Medicine and Allied Sciences, Defence Research and Development OrganisationInstitute of Nuclear Medicine and Allied Sciences, Defence Research and Development OrganisationInstitute of Nuclear Medicine and Allied Sciences, Defence Research and Development OrganisationAbstract Current models to study the hematopoietic syndrome largely rely on the uniform whole-body exposures. However, in the radio-nuclear accidents or terrorist events, exposure can be non-uniform. The data available on the non-uniform exposures is limited. Thus, we have developed a mice model for studying the hematopoietic syndrome in the non-uniform or partial body exposure scenarios using the localized cobalt60 gamma radiation exposure. Femur region of Strain ‘A’ male mice was exposed to doses ranging from 7 to 20 Gy. The 30 day survival assay showed 19 Gy as LD100 and 17 Gy as LD50. We measured an array of cytokines and important stem cell markers such as IFN-γ, IL-3, IL-6, GM-CSF, TNF-α, G-CSF, IL-1α, IL-1β, CD 34 and Sca 1. We found significant changes in IL-6, GM-CSF, TNF-α, G-CSF, and IL-1β levels compared to untreated groups and amplified levels of CD 34 and Sca 1 positive population in the irradiated mice compared to the untreated controls. Overall, we have developed a mouse model of the hematopoietic acute radiation syndrome that might be useful for understanding of the non-uniform body exposure scenarios. This may also be helpful in the screening of drugs intended for individuals suffering from radiation induced hematopoietic syndrome.https://doi.org/10.1038/s41598-020-80075-w |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
M. H. Yashavarddhan Ajay Kumar Sharma Pankaj Chaudhary Sania Bajaj Sukhvir Singh Sandeep Kumar Shukla |
spellingShingle |
M. H. Yashavarddhan Ajay Kumar Sharma Pankaj Chaudhary Sania Bajaj Sukhvir Singh Sandeep Kumar Shukla Development of hematopoietic syndrome mice model for localized radiation exposure Scientific Reports |
author_facet |
M. H. Yashavarddhan Ajay Kumar Sharma Pankaj Chaudhary Sania Bajaj Sukhvir Singh Sandeep Kumar Shukla |
author_sort |
M. H. Yashavarddhan |
title |
Development of hematopoietic syndrome mice model for localized radiation exposure |
title_short |
Development of hematopoietic syndrome mice model for localized radiation exposure |
title_full |
Development of hematopoietic syndrome mice model for localized radiation exposure |
title_fullStr |
Development of hematopoietic syndrome mice model for localized radiation exposure |
title_full_unstemmed |
Development of hematopoietic syndrome mice model for localized radiation exposure |
title_sort |
development of hematopoietic syndrome mice model for localized radiation exposure |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-01-01 |
description |
Abstract Current models to study the hematopoietic syndrome largely rely on the uniform whole-body exposures. However, in the radio-nuclear accidents or terrorist events, exposure can be non-uniform. The data available on the non-uniform exposures is limited. Thus, we have developed a mice model for studying the hematopoietic syndrome in the non-uniform or partial body exposure scenarios using the localized cobalt60 gamma radiation exposure. Femur region of Strain ‘A’ male mice was exposed to doses ranging from 7 to 20 Gy. The 30 day survival assay showed 19 Gy as LD100 and 17 Gy as LD50. We measured an array of cytokines and important stem cell markers such as IFN-γ, IL-3, IL-6, GM-CSF, TNF-α, G-CSF, IL-1α, IL-1β, CD 34 and Sca 1. We found significant changes in IL-6, GM-CSF, TNF-α, G-CSF, and IL-1β levels compared to untreated groups and amplified levels of CD 34 and Sca 1 positive population in the irradiated mice compared to the untreated controls. Overall, we have developed a mouse model of the hematopoietic acute radiation syndrome that might be useful for understanding of the non-uniform body exposure scenarios. This may also be helpful in the screening of drugs intended for individuals suffering from radiation induced hematopoietic syndrome. |
url |
https://doi.org/10.1038/s41598-020-80075-w |
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