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Non-induction of radioadaptive response in zebrafish embryos by neutrons
In vivo neutron-induced radioadaptive response (RAR) was studied using zebrafish (Danio rerio) embryos. The Neutron exposure Accelerator System for Biological Effect Experiments (NASBEE) facility at the National Institute of Radiological Sciences (NIRS), Japan, was employed to provide 2-MeV neutrons...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915534/ https://www.ncbi.nlm.nih.gov/pubmed/26850927 http://dx.doi.org/10.1093/jrr/rrv089 |
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author | Ng, Candy Y.P. Kong, Eva Y. Kobayashi, Alisa Suya, Noriyoshi Uchihori, Yukio Cheng, Shuk Han Konishi, Teruaki Yu, Kwan Ngok |
author_facet | Ng, Candy Y.P. Kong, Eva Y. Kobayashi, Alisa Suya, Noriyoshi Uchihori, Yukio Cheng, Shuk Han Konishi, Teruaki Yu, Kwan Ngok |
author_sort | Ng, Candy Y.P. |
collection | PubMed |
description | In vivo neutron-induced radioadaptive response (RAR) was studied using zebrafish (Danio rerio) embryos. The Neutron exposure Accelerator System for Biological Effect Experiments (NASBEE) facility at the National Institute of Radiological Sciences (NIRS), Japan, was employed to provide 2-MeV neutrons. Neutron doses of 0.6, 1, 25, 50 and 100 mGy were chosen as priming doses. An X-ray dose of 2 Gy was chosen as the challenging dose. Zebrafish embryos were dechorionated at 4 h post fertilization (hpf), irradiated with a chosen neutron dose at 5 hpf and the X-ray dose at 10 hpf. The responses of embryos were assessed at 25 hpf through the number of apoptotic signals. None of the neutron doses studied could induce RAR. Non-induction of RAR in embryos having received 0.6- and 1-mGy neutron doses was attributed to neutron-induced hormesis, which maintained the number of damaged cells at below the threshold for RAR induction. On the other hand, non-induction of RAR in embryos having received 25-, 50- and 100-mGy neutron doses was explained by gamma-ray hormesis, which mitigated neutron-induced damages through triggering high-fidelity DNA repair and removal of aberrant cells through apoptosis. Separate experimental results were obtained to verify that high-energy photons could disable RAR. Specifically, 5- or 10-mGy X-rays disabled the RAR induced by a priming dose of 0.88 mGy of alpha particles delivered to 5-hpf zebrafish embryos against a challenging dose of 2 Gy of X-rays delivered to the embryos at 10 hpf. |
format | Online Article Text |
id | pubmed-4915534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49155342016-06-22 Non-induction of radioadaptive response in zebrafish embryos by neutrons Ng, Candy Y.P. Kong, Eva Y. Kobayashi, Alisa Suya, Noriyoshi Uchihori, Yukio Cheng, Shuk Han Konishi, Teruaki Yu, Kwan Ngok J Radiat Res Regular Paper In vivo neutron-induced radioadaptive response (RAR) was studied using zebrafish (Danio rerio) embryos. The Neutron exposure Accelerator System for Biological Effect Experiments (NASBEE) facility at the National Institute of Radiological Sciences (NIRS), Japan, was employed to provide 2-MeV neutrons. Neutron doses of 0.6, 1, 25, 50 and 100 mGy were chosen as priming doses. An X-ray dose of 2 Gy was chosen as the challenging dose. Zebrafish embryos were dechorionated at 4 h post fertilization (hpf), irradiated with a chosen neutron dose at 5 hpf and the X-ray dose at 10 hpf. The responses of embryos were assessed at 25 hpf through the number of apoptotic signals. None of the neutron doses studied could induce RAR. Non-induction of RAR in embryos having received 0.6- and 1-mGy neutron doses was attributed to neutron-induced hormesis, which maintained the number of damaged cells at below the threshold for RAR induction. On the other hand, non-induction of RAR in embryos having received 25-, 50- and 100-mGy neutron doses was explained by gamma-ray hormesis, which mitigated neutron-induced damages through triggering high-fidelity DNA repair and removal of aberrant cells through apoptosis. Separate experimental results were obtained to verify that high-energy photons could disable RAR. Specifically, 5- or 10-mGy X-rays disabled the RAR induced by a priming dose of 0.88 mGy of alpha particles delivered to 5-hpf zebrafish embryos against a challenging dose of 2 Gy of X-rays delivered to the embryos at 10 hpf. Oxford University Press 2016-06 2016-06-21 /pmc/articles/PMC4915534/ /pubmed/26850927 http://dx.doi.org/10.1093/jrr/rrv089 Text en © The Author 2016. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Radiation Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Regular Paper Ng, Candy Y.P. Kong, Eva Y. Kobayashi, Alisa Suya, Noriyoshi Uchihori, Yukio Cheng, Shuk Han Konishi, Teruaki Yu, Kwan Ngok Non-induction of radioadaptive response in zebrafish embryos by neutrons |
title | Non-induction of radioadaptive response in zebrafish embryos by neutrons |
title_full | Non-induction of radioadaptive response in zebrafish embryos by neutrons |
title_fullStr | Non-induction of radioadaptive response in zebrafish embryos by neutrons |
title_full_unstemmed | Non-induction of radioadaptive response in zebrafish embryos by neutrons |
title_short | Non-induction of radioadaptive response in zebrafish embryos by neutrons |
title_sort | non-induction of radioadaptive response in zebrafish embryos by neutrons |
topic | Regular Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915534/ https://www.ncbi.nlm.nih.gov/pubmed/26850927 http://dx.doi.org/10.1093/jrr/rrv089 |
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