Transcriptional response to 131I exposure of rat thyroid gland.

Humans are exposed to 131I in medical diagnostics and treatment but also from nuclear accidents, and better knowledge of the molecular response in thyroid is needed. The aim of the study was to examine the transcriptional response in thyroid tissue 24 h after 131I administration in rats. The exposur...

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Main Authors: Nils Rudqvist, Johan Spetz, Emil Schüler, Toshima Z Parris, Britta Langen, Khalil Helou, Eva Forssell-Aronsson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5319760?pdf=render
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spelling doaj-39c276427c7a4c1f9cc8ad1ee11e72be2020-11-25T02:10:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01122e017179710.1371/journal.pone.0171797Transcriptional response to 131I exposure of rat thyroid gland.Nils RudqvistJohan SpetzEmil SchülerToshima Z ParrisBritta LangenKhalil HelouEva Forssell-AronssonHumans are exposed to 131I in medical diagnostics and treatment but also from nuclear accidents, and better knowledge of the molecular response in thyroid is needed. The aim of the study was to examine the transcriptional response in thyroid tissue 24 h after 131I administration in rats. The exposure levels were chosen to simulate both the clinical situation and the case of nuclear fallout. Thirty-six male rats were i.v. injected with 0-4700 kBq 131I, and killed at 24 h after injection (Dthyroid = 0.0058-3.0 Gy). Total RNA was extracted from individual thyroid tissue samples and mRNA levels were determined using oligonucleotide microarray technique. Differentially expressed transcripts were determined using Nexus Expression 3.0. Hierarchical clustering was performed in the R statistical computing environment. Pathway analysis was performed using the Ingenuity Pathway Analysis tool and the Gene Ontology database. T4 and TSH plasma concentrations were measured using ELISA. Totally, 429 differentially regulated transcripts were identified. Downregulation of thyroid hormone biosynthesis associated genes (e.g. thyroglobulin, thyroid peroxidase, the sodium-iodine symporter) was identified in some groups, and an impact on thyroid function was supported by the pathway analysis. Recurring downregulation of Dbp and Slc47a2 was found. Dbp exhibited a pattern with monotonous reduction of downregulation with absorbed dose at 0.0058-0.22 Gy. T4 plasma levels were increased and decreased in rats whose thyroids were exposed to 0.057 and 0.22 Gy, respectively. Different amounts of injected 131I gave distinct transcriptional responses in the rat thyroid. Transcriptional response related to thyroid function and changes in T4 plasma levels were found already at very low absorbed doses to thyroid.http://europepmc.org/articles/PMC5319760?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Nils Rudqvist
Johan Spetz
Emil Schüler
Toshima Z Parris
Britta Langen
Khalil Helou
Eva Forssell-Aronsson
spellingShingle Nils Rudqvist
Johan Spetz
Emil Schüler
Toshima Z Parris
Britta Langen
Khalil Helou
Eva Forssell-Aronsson
Transcriptional response to 131I exposure of rat thyroid gland.
PLoS ONE
author_facet Nils Rudqvist
Johan Spetz
Emil Schüler
Toshima Z Parris
Britta Langen
Khalil Helou
Eva Forssell-Aronsson
author_sort Nils Rudqvist
title Transcriptional response to 131I exposure of rat thyroid gland.
title_short Transcriptional response to 131I exposure of rat thyroid gland.
title_full Transcriptional response to 131I exposure of rat thyroid gland.
title_fullStr Transcriptional response to 131I exposure of rat thyroid gland.
title_full_unstemmed Transcriptional response to 131I exposure of rat thyroid gland.
title_sort transcriptional response to 131i exposure of rat thyroid gland.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Humans are exposed to 131I in medical diagnostics and treatment but also from nuclear accidents, and better knowledge of the molecular response in thyroid is needed. The aim of the study was to examine the transcriptional response in thyroid tissue 24 h after 131I administration in rats. The exposure levels were chosen to simulate both the clinical situation and the case of nuclear fallout. Thirty-six male rats were i.v. injected with 0-4700 kBq 131I, and killed at 24 h after injection (Dthyroid = 0.0058-3.0 Gy). Total RNA was extracted from individual thyroid tissue samples and mRNA levels were determined using oligonucleotide microarray technique. Differentially expressed transcripts were determined using Nexus Expression 3.0. Hierarchical clustering was performed in the R statistical computing environment. Pathway analysis was performed using the Ingenuity Pathway Analysis tool and the Gene Ontology database. T4 and TSH plasma concentrations were measured using ELISA. Totally, 429 differentially regulated transcripts were identified. Downregulation of thyroid hormone biosynthesis associated genes (e.g. thyroglobulin, thyroid peroxidase, the sodium-iodine symporter) was identified in some groups, and an impact on thyroid function was supported by the pathway analysis. Recurring downregulation of Dbp and Slc47a2 was found. Dbp exhibited a pattern with monotonous reduction of downregulation with absorbed dose at 0.0058-0.22 Gy. T4 plasma levels were increased and decreased in rats whose thyroids were exposed to 0.057 and 0.22 Gy, respectively. Different amounts of injected 131I gave distinct transcriptional responses in the rat thyroid. Transcriptional response related to thyroid function and changes in T4 plasma levels were found already at very low absorbed doses to thyroid.
url http://europepmc.org/articles/PMC5319760?pdf=render
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