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Age-related long-term response in rat thyroid tissue and plasma after internal low dose exposure to (131)I

(131)I is used clinically for therapy, and may be released during nuclear accidents. After the Chernobyl accident papillary thyroid carcinoma incidence increased in children, but not adults. The aims of this study were to compare (131)I irradiation-dependent differences in RNA and protein expression...

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Autores principales: Larsson, Malin, Rudqvist, Nils-Petter, Spetz, Johan, Parris, Toshima Z., Langen, Britta, Helou, Khalil, Forssell-Aronsson, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825795/
https://www.ncbi.nlm.nih.gov/pubmed/35136135
http://dx.doi.org/10.1038/s41598-022-06071-4
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author Larsson, Malin
Rudqvist, Nils-Petter
Spetz, Johan
Parris, Toshima Z.
Langen, Britta
Helou, Khalil
Forssell-Aronsson, Eva
author_facet Larsson, Malin
Rudqvist, Nils-Petter
Spetz, Johan
Parris, Toshima Z.
Langen, Britta
Helou, Khalil
Forssell-Aronsson, Eva
author_sort Larsson, Malin
collection PubMed
description (131)I is used clinically for therapy, and may be released during nuclear accidents. After the Chernobyl accident papillary thyroid carcinoma incidence increased in children, but not adults. The aims of this study were to compare (131)I irradiation-dependent differences in RNA and protein expression in the thyroid and plasma of young and adult rats, and identify potential age-dependent biomarkers for (131)I exposure. Twelve young (5 weeks) and twelve adult Sprague Dawley rats (17 weeks) were i.v. injected with 50 kBq (131)I (absorbed dose to thyroid = 0.1 Gy), and sixteen unexposed age-matched rats were used as controls. The rats were killed 3–9 months after administration. Microarray analysis was performed using RNA from thyroid samples, while LC–MS/MS analysis was performed on proteins extracted from thyroid tissue and plasma. Canonical pathways, biological functions and upstream regulators were analysed for the identified transcripts and proteins. Distinct age-dependent differences in gene and protein expression were observed. Novel biomarkers for thyroid (131)I exposure were identified: (PTH), age-dependent dose response (CA1, FTL1, PVALB (youngsters) and HSPB6 (adults)), thyroid function (Vegfb (adults)). Further validation using clinical samples are needed to explore the role of the identified biomarkers.
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spelling pubmed-88257952022-02-09 Age-related long-term response in rat thyroid tissue and plasma after internal low dose exposure to (131)I Larsson, Malin Rudqvist, Nils-Petter Spetz, Johan Parris, Toshima Z. Langen, Britta Helou, Khalil Forssell-Aronsson, Eva Sci Rep Article (131)I is used clinically for therapy, and may be released during nuclear accidents. After the Chernobyl accident papillary thyroid carcinoma incidence increased in children, but not adults. The aims of this study were to compare (131)I irradiation-dependent differences in RNA and protein expression in the thyroid and plasma of young and adult rats, and identify potential age-dependent biomarkers for (131)I exposure. Twelve young (5 weeks) and twelve adult Sprague Dawley rats (17 weeks) were i.v. injected with 50 kBq (131)I (absorbed dose to thyroid = 0.1 Gy), and sixteen unexposed age-matched rats were used as controls. The rats were killed 3–9 months after administration. Microarray analysis was performed using RNA from thyroid samples, while LC–MS/MS analysis was performed on proteins extracted from thyroid tissue and plasma. Canonical pathways, biological functions and upstream regulators were analysed for the identified transcripts and proteins. Distinct age-dependent differences in gene and protein expression were observed. Novel biomarkers for thyroid (131)I exposure were identified: (PTH), age-dependent dose response (CA1, FTL1, PVALB (youngsters) and HSPB6 (adults)), thyroid function (Vegfb (adults)). Further validation using clinical samples are needed to explore the role of the identified biomarkers. Nature Publishing Group UK 2022-02-08 /pmc/articles/PMC8825795/ /pubmed/35136135 http://dx.doi.org/10.1038/s41598-022-06071-4 Text en © The Author(s) 2022 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
Larsson, Malin
Rudqvist, Nils-Petter
Spetz, Johan
Parris, Toshima Z.
Langen, Britta
Helou, Khalil
Forssell-Aronsson, Eva
Age-related long-term response in rat thyroid tissue and plasma after internal low dose exposure to (131)I
title Age-related long-term response in rat thyroid tissue and plasma after internal low dose exposure to (131)I
title_full Age-related long-term response in rat thyroid tissue and plasma after internal low dose exposure to (131)I
title_fullStr Age-related long-term response in rat thyroid tissue and plasma after internal low dose exposure to (131)I
title_full_unstemmed Age-related long-term response in rat thyroid tissue and plasma after internal low dose exposure to (131)I
title_short Age-related long-term response in rat thyroid tissue and plasma after internal low dose exposure to (131)I
title_sort age-related long-term response in rat thyroid tissue and plasma after internal low dose exposure to (131)i
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825795/
https://www.ncbi.nlm.nih.gov/pubmed/35136135
http://dx.doi.org/10.1038/s41598-022-06071-4
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