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Increased Chromosome Aberrations in Cells Exposed Simultaneously to Simulated Microgravity and Radiation
Space radiation and microgravity (μG) are two major environmental stressors for humans in space travel. One of the fundamental questions in space biology research is whether the combined effects of μG and exposure to cosmic radiation are interactive. While studies addressing this question have been...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337712/ https://www.ncbi.nlm.nih.gov/pubmed/30583489 http://dx.doi.org/10.3390/ijms20010043 |
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author | Hada, Megumi Ikeda, Hiroko Rhone, Jordan R. Beitman, Andrew J. Plante, Ianik Souda, Hikaru Yoshida, Yukari Held, Kathryn D. Fujiwara, Keigi Saganti, Premkumar B. Takahashi, Akihisa |
author_facet | Hada, Megumi Ikeda, Hiroko Rhone, Jordan R. Beitman, Andrew J. Plante, Ianik Souda, Hikaru Yoshida, Yukari Held, Kathryn D. Fujiwara, Keigi Saganti, Premkumar B. Takahashi, Akihisa |
author_sort | Hada, Megumi |
collection | PubMed |
description | Space radiation and microgravity (μG) are two major environmental stressors for humans in space travel. One of the fundamental questions in space biology research is whether the combined effects of μG and exposure to cosmic radiation are interactive. While studies addressing this question have been carried out for half a century in space or using simulated μG on the ground, the reported results are ambiguous. For the assessment and management of human health risks in future Moon and Mars missions, it is necessary to obtain more basic data on the molecular and cellular responses to the combined effects of radiation and µG. Recently we incorporated a μG–irradiation system consisting of a 3D clinostat synchronized to a carbon-ion or X-ray irradiation system. Our new experimental setup allows us to avoid stopping clinostat rotation during irradiation, which was required in all other previous experiments. Using this system, human fibroblasts were exposed to X-rays or carbon ions under the simulated μG condition, and chromosomes were collected with the premature chromosome condensation method in the first mitosis. Chromosome aberrations (CA) were quantified by the 3-color fluorescent in situ hybridization (FISH) method. Cells exposed to irradiation under the simulated μG condition showed a higher frequency of both simple and complex types of CA compared to cells irradiated under the static condition by either X-rays or carbon ions. |
format | Online Article Text |
id | pubmed-6337712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63377122019-01-22 Increased Chromosome Aberrations in Cells Exposed Simultaneously to Simulated Microgravity and Radiation Hada, Megumi Ikeda, Hiroko Rhone, Jordan R. Beitman, Andrew J. Plante, Ianik Souda, Hikaru Yoshida, Yukari Held, Kathryn D. Fujiwara, Keigi Saganti, Premkumar B. Takahashi, Akihisa Int J Mol Sci Article Space radiation and microgravity (μG) are two major environmental stressors for humans in space travel. One of the fundamental questions in space biology research is whether the combined effects of μG and exposure to cosmic radiation are interactive. While studies addressing this question have been carried out for half a century in space or using simulated μG on the ground, the reported results are ambiguous. For the assessment and management of human health risks in future Moon and Mars missions, it is necessary to obtain more basic data on the molecular and cellular responses to the combined effects of radiation and µG. Recently we incorporated a μG–irradiation system consisting of a 3D clinostat synchronized to a carbon-ion or X-ray irradiation system. Our new experimental setup allows us to avoid stopping clinostat rotation during irradiation, which was required in all other previous experiments. Using this system, human fibroblasts were exposed to X-rays or carbon ions under the simulated μG condition, and chromosomes were collected with the premature chromosome condensation method in the first mitosis. Chromosome aberrations (CA) were quantified by the 3-color fluorescent in situ hybridization (FISH) method. Cells exposed to irradiation under the simulated μG condition showed a higher frequency of both simple and complex types of CA compared to cells irradiated under the static condition by either X-rays or carbon ions. MDPI 2018-12-22 /pmc/articles/PMC6337712/ /pubmed/30583489 http://dx.doi.org/10.3390/ijms20010043 Text en © 2018 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 Hada, Megumi Ikeda, Hiroko Rhone, Jordan R. Beitman, Andrew J. Plante, Ianik Souda, Hikaru Yoshida, Yukari Held, Kathryn D. Fujiwara, Keigi Saganti, Premkumar B. Takahashi, Akihisa Increased Chromosome Aberrations in Cells Exposed Simultaneously to Simulated Microgravity and Radiation |
title | Increased Chromosome Aberrations in Cells Exposed Simultaneously to Simulated Microgravity and Radiation |
title_full | Increased Chromosome Aberrations in Cells Exposed Simultaneously to Simulated Microgravity and Radiation |
title_fullStr | Increased Chromosome Aberrations in Cells Exposed Simultaneously to Simulated Microgravity and Radiation |
title_full_unstemmed | Increased Chromosome Aberrations in Cells Exposed Simultaneously to Simulated Microgravity and Radiation |
title_short | Increased Chromosome Aberrations in Cells Exposed Simultaneously to Simulated Microgravity and Radiation |
title_sort | increased chromosome aberrations in cells exposed simultaneously to simulated microgravity and radiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337712/ https://www.ncbi.nlm.nih.gov/pubmed/30583489 http://dx.doi.org/10.3390/ijms20010043 |
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