Evaluation of a multiplexed, multispecies nuclear receptor assay for chemical hazard assessment.
Ecotoxicology
Endocrine disruptors
Multiplexed assay
Nuclear receptor
Reporter gene
Zebrafish
Journal
Toxicology in vitro : an international journal published in association with BIBRA
ISSN: 1879-3177
Titre abrégé: Toxicol In Vitro
Pays: England
ID NLM: 8712158
Informations de publication
Date de publication:
Apr 2021
Apr 2021
Historique:
received:
19
06
2020
revised:
21
09
2020
accepted:
05
10
2020
pubmed:
14
10
2020
medline:
17
7
2022
entrez:
13
10
2020
Statut:
ppublish
Résumé
Sensitivity to potential endocrine disrupting chemicals in the environment varies across species and is influenced by sequence conservation of their nuclear receptor targets. Here, we evaluated a multiplexed, in vitro assay testing receptors relevant to endocrine and metabolic disruption from five species. The TRANS-FACTORIAL™ system of human nuclear receptors was modified to include additional species: mouse (Mus musculus), frog (Xenopus laevis), zebrafish (Danio rerio), chicken (Gallus gallus), and turtle (Chrysemys picta). Receptors regulating endocrine function and xenobiotic recognition were included, specifically: ERα, ERβ, AR, TRα, TRβ, PPARγ and PXR. The assay, ECOTOX-FACTORIAL™, was evaluated with 191 chemicals enriched with known receptor ligands. Hierarchical clustering of potency values demonstrated strong coherence of receptor families. Interspecies comparisons of responses within a receptor family showed moderate to high concordance for potencies under 50 μM. PPARγ showed high concordance between mammalian species, 89%, but only 63% between mammalian and zebrafish. For chemicals with potencies below 1 μM, concordances were 89-100% for all receptors except PXR. Concordance showed a strong positive relationship to ligand-binding domain sequence similarity and critical amino acid residues obtained by the Sequence Alignment to Predict Across Species Susceptibility (SeqAPASS) tool. In combination with SeqAPASS, ECOTOX-FACTORIAL may provide efficient screening of important receptors to identify species of high priority for effects monitoring.
Identifiants
pubmed: 33049310
pii: S0887-2333(20)30566-X
doi: 10.1016/j.tiv.2020.105016
pii:
doi:
Substances chimiques
Hazardous Substances
0
Receptors, Cytoplasmic and Nuclear
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
105016Informations de copyright
Copyright © 2020. Published by Elsevier Ltd.