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In vitro effects of 0 to 120 Grays of irradiation on bone viability and release of growth factors
BACKGROUND: High dose radiation therapy is commonly used in maxillofacial surgeries to treat a number of head and neck tumors. Despite its widespread use, little information is available regarding the effects of irradiation on bone cell viability and release of growth factors following dose-dependen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948100/ https://www.ncbi.nlm.nih.gov/pubmed/27431387 http://dx.doi.org/10.1186/s12903-016-0241-9 |
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author | Sawada, Kosaku Fujioka-Kobayashi, Masako Kobayashi, Eizaburo Brömme, Jens O. Schaller, Benoit Miron, Richard J. |
author_facet | Sawada, Kosaku Fujioka-Kobayashi, Masako Kobayashi, Eizaburo Brömme, Jens O. Schaller, Benoit Miron, Richard J. |
author_sort | Sawada, Kosaku |
collection | PubMed |
description | BACKGROUND: High dose radiation therapy is commonly used in maxillofacial surgeries to treat a number of head and neck tumors. Despite its widespread use, little information is available regarding the effects of irradiation on bone cell viability and release of growth factors following dose-dependent irradiation. METHODS: Bone samples were collected from porcine mandibular cortical bone and irradiated at doses of 0, 7.5, 15, 30, 60 and 120 Grays. Thereafter, cell viability was quantified, and the release of growth factors including TGFβ1, BMP2, VEGF, IL1β and RANKL were investigated over time. RESULTS: It was observed that at only 7.5Gy of irradiation, over 85 % of cells were non-vital and by 60 Gy, all cells underwent apoptosis. Furthermore, over a 7-fold decrease in VEGF and a 2-fold decrease in TGFβ1 were observed following irradiation at all tested doses. Little change was observed for BMP2 and IL1β whereas RANKL was significantly increased for all irradiated samples. CONCLUSIONS: These results demonstrate the pronounced effects of irradiation on bone-cell vitality and subsequent release of growth factors. Interestingly, the largest observed change in gene expression was the 7-fold decrease in VEGF protein following irradiation. Future research aimed at improving our understanding of bone following irradiation is necessary to further improve future clinical treatments. |
format | Online Article Text |
id | pubmed-4948100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49481002016-07-19 In vitro effects of 0 to 120 Grays of irradiation on bone viability and release of growth factors Sawada, Kosaku Fujioka-Kobayashi, Masako Kobayashi, Eizaburo Brömme, Jens O. Schaller, Benoit Miron, Richard J. BMC Oral Health Research Article BACKGROUND: High dose radiation therapy is commonly used in maxillofacial surgeries to treat a number of head and neck tumors. Despite its widespread use, little information is available regarding the effects of irradiation on bone cell viability and release of growth factors following dose-dependent irradiation. METHODS: Bone samples were collected from porcine mandibular cortical bone and irradiated at doses of 0, 7.5, 15, 30, 60 and 120 Grays. Thereafter, cell viability was quantified, and the release of growth factors including TGFβ1, BMP2, VEGF, IL1β and RANKL were investigated over time. RESULTS: It was observed that at only 7.5Gy of irradiation, over 85 % of cells were non-vital and by 60 Gy, all cells underwent apoptosis. Furthermore, over a 7-fold decrease in VEGF and a 2-fold decrease in TGFβ1 were observed following irradiation at all tested doses. Little change was observed for BMP2 and IL1β whereas RANKL was significantly increased for all irradiated samples. CONCLUSIONS: These results demonstrate the pronounced effects of irradiation on bone-cell vitality and subsequent release of growth factors. Interestingly, the largest observed change in gene expression was the 7-fold decrease in VEGF protein following irradiation. Future research aimed at improving our understanding of bone following irradiation is necessary to further improve future clinical treatments. BioMed Central 2016-07-04 /pmc/articles/PMC4948100/ /pubmed/27431387 http://dx.doi.org/10.1186/s12903-016-0241-9 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Sawada, Kosaku Fujioka-Kobayashi, Masako Kobayashi, Eizaburo Brömme, Jens O. Schaller, Benoit Miron, Richard J. In vitro effects of 0 to 120 Grays of irradiation on bone viability and release of growth factors |
title | In vitro effects of 0 to 120 Grays of irradiation on bone viability and release of growth factors |
title_full | In vitro effects of 0 to 120 Grays of irradiation on bone viability and release of growth factors |
title_fullStr | In vitro effects of 0 to 120 Grays of irradiation on bone viability and release of growth factors |
title_full_unstemmed | In vitro effects of 0 to 120 Grays of irradiation on bone viability and release of growth factors |
title_short | In vitro effects of 0 to 120 Grays of irradiation on bone viability and release of growth factors |
title_sort | in vitro effects of 0 to 120 grays of irradiation on bone viability and release of growth factors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948100/ https://www.ncbi.nlm.nih.gov/pubmed/27431387 http://dx.doi.org/10.1186/s12903-016-0241-9 |
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