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Radiosafe micro-computed tomography for longitudinal evaluation of murine disease models
Implementation of in vivo high-resolution micro-computed tomography (µCT), a powerful tool for longitudinal analysis of murine lung disease models, is hampered by the lack of data on cumulative low-dose radiation effects on the investigated disease models. We aimed to measure radiation doses and eff...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879529/ https://www.ncbi.nlm.nih.gov/pubmed/31772203 http://dx.doi.org/10.1038/s41598-019-53876-x |
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author | Berghen, Nathalie Dekoster, Kaat Marien, Eyra Dabin, Jérémie Hillen, Amy Wouters, Jens Deferme, Jasmine Vosselman, Thibault Tiest, Eline Lox, Marleen Vanoirbeek, Jeroen De Langhe, Ellen Bogaerts, Ria Hoylaerts, Marc Lories, Rik Vande Velde, Greetje |
author_facet | Berghen, Nathalie Dekoster, Kaat Marien, Eyra Dabin, Jérémie Hillen, Amy Wouters, Jens Deferme, Jasmine Vosselman, Thibault Tiest, Eline Lox, Marleen Vanoirbeek, Jeroen De Langhe, Ellen Bogaerts, Ria Hoylaerts, Marc Lories, Rik Vande Velde, Greetje |
author_sort | Berghen, Nathalie |
collection | PubMed |
description | Implementation of in vivo high-resolution micro-computed tomography (µCT), a powerful tool for longitudinal analysis of murine lung disease models, is hampered by the lack of data on cumulative low-dose radiation effects on the investigated disease models. We aimed to measure radiation doses and effects of repeated µCT scans, to establish cumulative radiation levels and scan protocols without relevant toxicity. Lung metastasis, inflammation and fibrosis models and healthy mice were weekly scanned over one-month with µCT using high-resolution respiratory-gated 4D and expiration-weighted 3D protocols, comparing 5-times weekly scanned animals with controls. Radiation dose was measured by ionization chamber, optical fiberradioluminescence probe and thermoluminescent detectors in a mouse phantom. Dose effects were evaluated by in vivo µCT and bioluminescence imaging read-outs, gold standard endpoint evaluation and blood cell counts. Weekly exposure to 4D µCT, dose of 540–699 mGy/scan, did not alter lung metastatic load nor affected healthy mice. We found a disease-independent decrease in circulating blood platelets and lymphocytes after repeated 4D µCT. This effect was eliminated by optimizing a 3D protocol, reducing dose to 180–233 mGy/scan while maintaining equally high-quality images. We established µCT safety limits and protocols for weekly repeated whole-body acquisitions with proven safety for the overall health status, lung, disease process and host responses under investigation, including the radiosensitive blood cell compartment. |
format | Online Article Text |
id | pubmed-6879529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68795292019-12-05 Radiosafe micro-computed tomography for longitudinal evaluation of murine disease models Berghen, Nathalie Dekoster, Kaat Marien, Eyra Dabin, Jérémie Hillen, Amy Wouters, Jens Deferme, Jasmine Vosselman, Thibault Tiest, Eline Lox, Marleen Vanoirbeek, Jeroen De Langhe, Ellen Bogaerts, Ria Hoylaerts, Marc Lories, Rik Vande Velde, Greetje Sci Rep Article Implementation of in vivo high-resolution micro-computed tomography (µCT), a powerful tool for longitudinal analysis of murine lung disease models, is hampered by the lack of data on cumulative low-dose radiation effects on the investigated disease models. We aimed to measure radiation doses and effects of repeated µCT scans, to establish cumulative radiation levels and scan protocols without relevant toxicity. Lung metastasis, inflammation and fibrosis models and healthy mice were weekly scanned over one-month with µCT using high-resolution respiratory-gated 4D and expiration-weighted 3D protocols, comparing 5-times weekly scanned animals with controls. Radiation dose was measured by ionization chamber, optical fiberradioluminescence probe and thermoluminescent detectors in a mouse phantom. Dose effects were evaluated by in vivo µCT and bioluminescence imaging read-outs, gold standard endpoint evaluation and blood cell counts. Weekly exposure to 4D µCT, dose of 540–699 mGy/scan, did not alter lung metastatic load nor affected healthy mice. We found a disease-independent decrease in circulating blood platelets and lymphocytes after repeated 4D µCT. This effect was eliminated by optimizing a 3D protocol, reducing dose to 180–233 mGy/scan while maintaining equally high-quality images. We established µCT safety limits and protocols for weekly repeated whole-body acquisitions with proven safety for the overall health status, lung, disease process and host responses under investigation, including the radiosensitive blood cell compartment. Nature Publishing Group UK 2019-11-26 /pmc/articles/PMC6879529/ /pubmed/31772203 http://dx.doi.org/10.1038/s41598-019-53876-x Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Berghen, Nathalie Dekoster, Kaat Marien, Eyra Dabin, Jérémie Hillen, Amy Wouters, Jens Deferme, Jasmine Vosselman, Thibault Tiest, Eline Lox, Marleen Vanoirbeek, Jeroen De Langhe, Ellen Bogaerts, Ria Hoylaerts, Marc Lories, Rik Vande Velde, Greetje Radiosafe micro-computed tomography for longitudinal evaluation of murine disease models |
title | Radiosafe micro-computed tomography for longitudinal evaluation of murine disease models |
title_full | Radiosafe micro-computed tomography for longitudinal evaluation of murine disease models |
title_fullStr | Radiosafe micro-computed tomography for longitudinal evaluation of murine disease models |
title_full_unstemmed | Radiosafe micro-computed tomography for longitudinal evaluation of murine disease models |
title_short | Radiosafe micro-computed tomography for longitudinal evaluation of murine disease models |
title_sort | radiosafe micro-computed tomography for longitudinal evaluation of murine disease models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879529/ https://www.ncbi.nlm.nih.gov/pubmed/31772203 http://dx.doi.org/10.1038/s41598-019-53876-x |
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