PUBLICATION

Triclosan Lacks Anti-Estrogenic Effects in Zebrafish Cells but Modulates Estrogen Response in Zebrafish Embryos

Authors
Serra, H., Brion, F., Porcher, J.M., Budzinski, H., Aït-Aïssa, S.
ID
ZDB-PUB-180418-28
Date
2018
Source
International Journal of Molecular Sciences   19(4): (Journal)
Registered Authors
Keywords
brain aromatase, estrogen receptor, in vitro, in vivo, triclosan, zebrafish
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Cell Line
  • Estradiol/metabolism*
  • Gene Expression Regulation, Developmental/drug effects
  • Genes, Reporter
  • Humans
  • MCF-7 Cells
  • Receptors, Estrogen/metabolism*
  • Transcription, Genetic/drug effects*
  • Triclosan/pharmacology*
  • Zebrafish/embryology*
  • Zebrafish/genetics
  • Zebrafish/metabolism
  • Zebrafish Proteins/metabolism
PubMed
29649157 Full text @ Int. J. Mol. Sci.
Abstract
Triclosan (TCS), an antimicrobial agent widely found in the aquatic environment, is suspected to act as an endocrine disrupting compound, however mechanistic information is lacking in regards to aquatic species. This study assessed the ability of TCS to interfere with estrogen receptor (ER) transcriptional activity, in zebrafish-specific in vitro and in vivo reporter gene assays. We report that TCS exhibits a lack of either agonistic or antagonistic effects on a panel of ER-expressing zebrafish (ZELH-zfERα and -zfERβ) and human (MELN) cell lines. At the organism level, TCS at concentrations of up to 0.3 µM had no effect on ER-regulated brain aromatase gene expression in transgenic cyp19a1b-GFP zebrafish embryos. At a concentration of 1 µM, TCS interfered with the E2 response in an ambivalent manner by potentializing a low E2 response (0.625 nM), but decreasing a high E2 response (10 nM). Altogether, our study suggests that while modulation of ER-regulated genes by TCS may occur in zebrafish, it does so irrespective of a direct binding and activation of zfERs.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping