Retene causes multifunctional transcriptomic changes in the heart of rainbow trout (Oncorhynchus mykiss) embryos

Environ Toxicol Pharmacol. 2016 Jan:41:95-102. doi: 10.1016/j.etap.2015.11.015. Epub 2015 Nov 28.

Abstract

Fish are particularly sensitive to aryl hydrocarbon receptor (AhR)-mediated developmental toxicity. The molecular mechanisms behind these adverse effects have remained largely unresolved in salmonids, and for AhR-agonistic polycyclic aromatic hydrocarbons (PAHs). This study explored the cardiac transcriptome of rainbow trout (Oncorhynchus mykiss) eleuteroembryos exposed to retene, an AhR-agonistic PAH. The embryos were exposed to retene (nominal concentration 32 μg/L) and control, their hearts were collected before, at and after the onset of the visible signs of developmental toxicity, and transcriptomic changes were studied by microarray analysis. Retene up- or down-regulated 122 genes. The largest Gene Ontology groups were signal transduction, transcription, apoptosis, cell growth, cytoskeleton, cell adhesion/mobility, cardiovascular development, xenobiotic metabolism, protein metabolism, lipid metabolism and transport, and amino acid metabolism. Together these findings suggest that retene affects multiple signaling cascades in the heart of rainbow trout embryos, and potentially disturbs processes related to cardiovascular development and function.

Keywords: Dioxin-like toxicity; Fish embryo; Transcriptomics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Embryo, Nonmammalian / drug effects
  • Embryonic Development / drug effects
  • Gene Expression Profiling / methods
  • Gene Expression Regulation, Developmental / drug effects*
  • Heart / drug effects*
  • Heart / growth & development
  • Oligonucleotide Array Sequence Analysis / methods
  • Oncorhynchus mykiss / embryology
  • Oncorhynchus mykiss / genetics*
  • Phenanthrenes / toxicity*

Substances

  • Phenanthrenes
  • retene