Potential roles of nuclear receptors in mediating neurodevelopmental toxicity of known endocrine-disrupting chemicals in ascidian embryos

Mol Reprod Dev. 2019 Oct;86(10):1333-1347. doi: 10.1002/mrd.23219. Epub 2019 Jun 19.

Abstract

Endocrine Disrupting Chemicals (EDCs) are molecules able to interfere with the vertebrate hormonal system in different ways, a major one being the modification of the activity of nuclear receptors (NRs). Several NRs are expressed in the vertebrate brain during embryonic development and these NRs are suspected to be responsible for the neurodevelopmental defects induced by exposure to EDCs in fishes or amphibians and to participate in several neurodevelopmental disorders observed in humans. Known EDCs exert toxicity not only on vertebrate forms of marine life but also on marine invertebrates. However, because hormonal systems of invertebrates are poorly understood, it is not clear whether the teratogenic effects of known EDCs are because of endocrine disruption. The most conserved actors of endocrine systems are the NRs which are present in all metazoan genomes but their functions in invertebrate organisms are still insufficiently characterized. EDCs like bisphenol A have recently been shown to affect neurodevelopment in marine invertebrate chordates called ascidians. Because such phenotypes can be mediated by NRs expressed in the ascidian embryo, we review all the information available about NRs expression during ascidian embryogenesis and discuss their possible involvement in the neurodevelopmental phenotypes induced by EDCs.

Keywords: endocrine-disrupting chemicals; marine invertebrate; mode-of-action; neurodevelopment; nuclear receptors.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Embryo, Nonmammalian / drug effects
  • Embryonic Development / drug effects
  • Endocrine Disruptors / toxicity*
  • Models, Biological
  • Nervous System* / drug effects
  • Nervous System* / embryology
  • Nervous System* / growth & development
  • Neurotoxins / toxicity*
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Urochordata* / drug effects
  • Urochordata* / embryology
  • Urochordata* / growth & development

Substances

  • Endocrine Disruptors
  • Neurotoxins
  • Receptors, Cytoplasmic and Nuclear