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Pilot investigation on the dose-dependent impact of irradiation on primary human alveolar osteoblasts in vitro
Radiotherapy of head and neck squamous cell carcinoma can lead to long-term complications like osteoradionecrosis, resulting in severe impairment of the jawbone. Current standard procedures require a 6-month wait after irradiation before dental reconstruction can begin. A comprehensive characterizat...
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/PMC8494843/ https://www.ncbi.nlm.nih.gov/pubmed/34615948 http://dx.doi.org/10.1038/s41598-021-99323-8 |
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author | Amler, Anna-Klara Schlauch, Domenic Tüzüner, Selin Thomas, Alexander Neckel, Norbert Tinhofer, Ingeborg Heiland, Max Lauster, Roland Kloke, Lutz Stromberger, Carmen Nahles, Susanne |
author_facet | Amler, Anna-Klara Schlauch, Domenic Tüzüner, Selin Thomas, Alexander Neckel, Norbert Tinhofer, Ingeborg Heiland, Max Lauster, Roland Kloke, Lutz Stromberger, Carmen Nahles, Susanne |
author_sort | Amler, Anna-Klara |
collection | PubMed |
description | Radiotherapy of head and neck squamous cell carcinoma can lead to long-term complications like osteoradionecrosis, resulting in severe impairment of the jawbone. Current standard procedures require a 6-month wait after irradiation before dental reconstruction can begin. A comprehensive characterization of the irradiation-induced molecular and functional changes in bone cells could allow the development of novel strategies for an earlier successful dental reconstruction in patients treated by radiotherapy. The impact of ionizing radiation on the bone-forming alveolar osteoblasts remains however elusive, as previous studies have relied on animal-based models and fetal or animal-derived cell lines. This study presents the first in vitro data obtained from primary human alveolar osteoblasts. Primary human alveolar osteoblasts were isolated from healthy donors and expanded. After X-ray irradiation with 2, 6 and 10 Gy, cells were cultivated under osteogenic conditions and analyzed regarding their proliferation, mineralization, and expression of marker genes and proteins. Proliferation of osteoblasts decreased in a dose-dependent manner. While cells recovered from irradiation with 2 Gy, application of 6 and 10 Gy doses not only led to a permanent impairment of proliferation, but also resulted in altered cell morphology and a disturbed structure of the extracellular matrix as demonstrated by immunostaining of collagen I and fibronectin. Following irradiation with any of the examined doses, a decrease of marker gene expression levels was observed for most of the investigated genes, revealing interindividual differences. Primary human alveolar osteoblasts presented a considerably changed phenotype after irradiation, depending on the dose administered. Mechanisms for these findings need to be further investigated. This could facilitate improved patient care by re-evaluating current standard procedures and investigating faster and safer reconstruction concepts, thus improving quality of life and social integrity. |
format | Online Article Text |
id | pubmed-8494843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84948432021-10-08 Pilot investigation on the dose-dependent impact of irradiation on primary human alveolar osteoblasts in vitro Amler, Anna-Klara Schlauch, Domenic Tüzüner, Selin Thomas, Alexander Neckel, Norbert Tinhofer, Ingeborg Heiland, Max Lauster, Roland Kloke, Lutz Stromberger, Carmen Nahles, Susanne Sci Rep Article Radiotherapy of head and neck squamous cell carcinoma can lead to long-term complications like osteoradionecrosis, resulting in severe impairment of the jawbone. Current standard procedures require a 6-month wait after irradiation before dental reconstruction can begin. A comprehensive characterization of the irradiation-induced molecular and functional changes in bone cells could allow the development of novel strategies for an earlier successful dental reconstruction in patients treated by radiotherapy. The impact of ionizing radiation on the bone-forming alveolar osteoblasts remains however elusive, as previous studies have relied on animal-based models and fetal or animal-derived cell lines. This study presents the first in vitro data obtained from primary human alveolar osteoblasts. Primary human alveolar osteoblasts were isolated from healthy donors and expanded. After X-ray irradiation with 2, 6 and 10 Gy, cells were cultivated under osteogenic conditions and analyzed regarding their proliferation, mineralization, and expression of marker genes and proteins. Proliferation of osteoblasts decreased in a dose-dependent manner. While cells recovered from irradiation with 2 Gy, application of 6 and 10 Gy doses not only led to a permanent impairment of proliferation, but also resulted in altered cell morphology and a disturbed structure of the extracellular matrix as demonstrated by immunostaining of collagen I and fibronectin. Following irradiation with any of the examined doses, a decrease of marker gene expression levels was observed for most of the investigated genes, revealing interindividual differences. Primary human alveolar osteoblasts presented a considerably changed phenotype after irradiation, depending on the dose administered. Mechanisms for these findings need to be further investigated. This could facilitate improved patient care by re-evaluating current standard procedures and investigating faster and safer reconstruction concepts, thus improving quality of life and social integrity. Nature Publishing Group UK 2021-10-06 /pmc/articles/PMC8494843/ /pubmed/34615948 http://dx.doi.org/10.1038/s41598-021-99323-8 Text en © The Author(s) 2021 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 Amler, Anna-Klara Schlauch, Domenic Tüzüner, Selin Thomas, Alexander Neckel, Norbert Tinhofer, Ingeborg Heiland, Max Lauster, Roland Kloke, Lutz Stromberger, Carmen Nahles, Susanne Pilot investigation on the dose-dependent impact of irradiation on primary human alveolar osteoblasts in vitro |
title | Pilot investigation on the dose-dependent impact of irradiation on primary human alveolar osteoblasts in vitro |
title_full | Pilot investigation on the dose-dependent impact of irradiation on primary human alveolar osteoblasts in vitro |
title_fullStr | Pilot investigation on the dose-dependent impact of irradiation on primary human alveolar osteoblasts in vitro |
title_full_unstemmed | Pilot investigation on the dose-dependent impact of irradiation on primary human alveolar osteoblasts in vitro |
title_short | Pilot investigation on the dose-dependent impact of irradiation on primary human alveolar osteoblasts in vitro |
title_sort | pilot investigation on the dose-dependent impact of irradiation on primary human alveolar osteoblasts in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494843/ https://www.ncbi.nlm.nih.gov/pubmed/34615948 http://dx.doi.org/10.1038/s41598-021-99323-8 |
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