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Advancing in vitro assessment of iodide uptake inhibition: integrating a novel biotransformation pretreatment step
P. Kumari, S. Lungu-Mitea, J. Novák, K. Hilscherová
Language English Country Germany
Document type Journal Article
Grant support
CZ.02.01.01/00/22_008/0004644
Ministerstvo Školství, Mládeže a Tělovýchovy
LM2023069
Ministerstvo Školství, Mládeže a Tělovýchovy
857560
Horizon 2020 Framework Programme
825753
Horizon 2020 Framework Programme
- MeSH
- Biological Assay methods MeSH
- Biotransformation MeSH
- Cell Line MeSH
- Endocrine Disruptors * toxicity MeSH
- Thyroid Hormones metabolism MeSH
- Iodides * metabolism MeSH
- Rats MeSH
- Humans MeSH
- Thyroid Gland metabolism drug effects cytology MeSH
- Symporters * antagonists & inhibitors metabolism genetics MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
Thyroid hormones (TH) are essential for vertebrate development, growth, and metabolism. The increasing prevalence of anthropogenic chemicals with TH-disrupting potential highlights the urgent need for advanced methods to assess their impact on TH homeostasis. Inhibition of the sodium-iodide symporter (NIS) has been identified as a key molecular initiating event disrupting the TH system across species, with significant relevance for diagnostic and therapeutic applications in various carcinomas. This study presents in vitro bioassays for evaluating the effects of compounds on iodide uptake into cells, a critical step in TH production mediated by NIS. Two novel stably transfected human cell lines overexpressing human NIS were employed along with a rat thyroid cell model FRTL-5, using colorimetric Sandell-Kolthoff (SK) reaction for iodide detection. The results from 23 model compounds demonstrate comparability across various in vitro models and radioactivity-based assays. To enhance physiological relevance, an external biotransformation system (BTS) was integrated and optimized for live-cell compatibility without inducing cytotoxicity or interfering with the assay. Compounds identified as NIS inhibitors were evaluated using the BTS-augmented assay, which revealed that metabolic activity mitigated the inhibitory effects of some chemicals. The augmented assay exhibited strong concordance with in vivo and in silico biotransformation data. Protein sequence alignment confirmed high conservation of NIS functional domains across vertebrates, reinforcing the cross-species applicability of the findings. The SK-based NIS assay, with optional BTS integration, represents a sensitive, robust, and high-throughput amendable alternative to radioactivity-based methods, for characterizing the impacts of individual compounds and complex environmental mixtures on TH homeostasis.
References provided by Crossref.org
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