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Repair Kinetics of DNA Double Strand Breaks Induced by Simulated Space Radiation
Radiation is unavoidable in space. Energetic particles in space radiation are reported to induce cluster DNA damage that is difficult to repair. In this study, normal human fibroblasts were irradiated with components of space radiation such as proton, helium, or carbon ion beams. Immunostaining for...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763067/ https://www.ncbi.nlm.nih.gov/pubmed/33321941 http://dx.doi.org/10.3390/life10120341 |
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author | Oizumi, Takashi Ohno, Rieko Yamabe, Souichiro Funayama, Tomoo Nakamura, Asako J. |
author_facet | Oizumi, Takashi Ohno, Rieko Yamabe, Souichiro Funayama, Tomoo Nakamura, Asako J. |
author_sort | Oizumi, Takashi |
collection | PubMed |
description | Radiation is unavoidable in space. Energetic particles in space radiation are reported to induce cluster DNA damage that is difficult to repair. In this study, normal human fibroblasts were irradiated with components of space radiation such as proton, helium, or carbon ion beams. Immunostaining for γ-H2AX and 53BP1 was performed over time to evaluate the kinetics of DNA damage repair. Our data clearly show that the repair kinetics of DNA double strand breaks (DSBs) induced by carbon ion irradiation, which has a high linear energy transfer (LET), are significantly slower than those of proton and helium ion irradiation. Mixed irradiation with carbon ions, followed by helium ions, did not have an additive effect on the DSB repair kinetics. Interestingly, the mean γ-H2AX focus size was shown to increase with LET, suggesting that the delay in repair kinetics was due to damage that is more complex. Further, the 53BP1 focus size also increased in an LET-dependent manner. Repair of DSBs, characterized by large 53BP1 foci, was a slow process within the biphasic kinetics of DSB repair, suggesting non-homologous end joining with error-prone end resection. Our data suggest that the biological effects of space radiation may be significantly influenced by the dose as well as the type of radiation exposure. |
format | Online Article Text |
id | pubmed-7763067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77630672020-12-27 Repair Kinetics of DNA Double Strand Breaks Induced by Simulated Space Radiation Oizumi, Takashi Ohno, Rieko Yamabe, Souichiro Funayama, Tomoo Nakamura, Asako J. Life (Basel) Article Radiation is unavoidable in space. Energetic particles in space radiation are reported to induce cluster DNA damage that is difficult to repair. In this study, normal human fibroblasts were irradiated with components of space radiation such as proton, helium, or carbon ion beams. Immunostaining for γ-H2AX and 53BP1 was performed over time to evaluate the kinetics of DNA damage repair. Our data clearly show that the repair kinetics of DNA double strand breaks (DSBs) induced by carbon ion irradiation, which has a high linear energy transfer (LET), are significantly slower than those of proton and helium ion irradiation. Mixed irradiation with carbon ions, followed by helium ions, did not have an additive effect on the DSB repair kinetics. Interestingly, the mean γ-H2AX focus size was shown to increase with LET, suggesting that the delay in repair kinetics was due to damage that is more complex. Further, the 53BP1 focus size also increased in an LET-dependent manner. Repair of DSBs, characterized by large 53BP1 foci, was a slow process within the biphasic kinetics of DSB repair, suggesting non-homologous end joining with error-prone end resection. Our data suggest that the biological effects of space radiation may be significantly influenced by the dose as well as the type of radiation exposure. MDPI 2020-12-10 /pmc/articles/PMC7763067/ /pubmed/33321941 http://dx.doi.org/10.3390/life10120341 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Oizumi, Takashi Ohno, Rieko Yamabe, Souichiro Funayama, Tomoo Nakamura, Asako J. Repair Kinetics of DNA Double Strand Breaks Induced by Simulated Space Radiation |
title | Repair Kinetics of DNA Double Strand Breaks Induced by Simulated Space Radiation |
title_full | Repair Kinetics of DNA Double Strand Breaks Induced by Simulated Space Radiation |
title_fullStr | Repair Kinetics of DNA Double Strand Breaks Induced by Simulated Space Radiation |
title_full_unstemmed | Repair Kinetics of DNA Double Strand Breaks Induced by Simulated Space Radiation |
title_short | Repair Kinetics of DNA Double Strand Breaks Induced by Simulated Space Radiation |
title_sort | repair kinetics of dna double strand breaks induced by simulated space radiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763067/ https://www.ncbi.nlm.nih.gov/pubmed/33321941 http://dx.doi.org/10.3390/life10120341 |
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