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Development of hematopoietic syndrome mice model for localized radiation exposure
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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794306/ https://www.ncbi.nlm.nih.gov/pubmed/33420217 http://dx.doi.org/10.1038/s41598-020-80075-w |
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author | Yashavarddhan, M. H. Sharma, Ajay Kumar Chaudhary, Pankaj Bajaj, Sania Singh, Sukhvir Shukla, Sandeep Kumar |
author_facet | Yashavarddhan, M. H. Sharma, Ajay Kumar Chaudhary, Pankaj Bajaj, Sania Singh, Sukhvir Shukla, Sandeep Kumar |
author_sort | Yashavarddhan, M. H. |
collection | PubMed |
description | 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 cobalt(60) 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 LD(100) and 17 Gy as LD(50.) 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. |
format | Online Article Text |
id | pubmed-7794306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77943062021-01-11 Development of hematopoietic syndrome mice model for localized radiation exposure Yashavarddhan, M. H. Sharma, Ajay Kumar Chaudhary, Pankaj Bajaj, Sania Singh, Sukhvir Shukla, Sandeep Kumar Sci Rep Article 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 cobalt(60) 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 LD(100) and 17 Gy as LD(50.) 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. Nature Publishing Group UK 2021-01-08 /pmc/articles/PMC7794306/ /pubmed/33420217 http://dx.doi.org/10.1038/s41598-020-80075-w Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yashavarddhan, M. H. Sharma, Ajay Kumar Chaudhary, Pankaj Bajaj, Sania Singh, Sukhvir Shukla, Sandeep Kumar Development of hematopoietic syndrome mice model for localized radiation exposure |
title | 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_short | Development of hematopoietic syndrome mice model for localized radiation exposure |
title_sort | development of hematopoietic syndrome mice model for localized radiation exposure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794306/ https://www.ncbi.nlm.nih.gov/pubmed/33420217 http://dx.doi.org/10.1038/s41598-020-80075-w |
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