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National Institute of Environmental Health Sciences

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Your Environment. Your Health.

Publication Detail

Title: Trichloroethylene perturbs HNF4a expression and activity in the developing chick heart.

Authors: Harris, Alondra P; Ismail, Kareem A; Nunez, Martha; Martopullo, Ira; Lencinas, Alejandro; Selmin, Ornella I; Runyan, Raymond B

Published In Toxicol Lett, (2018 Mar 15)

Abstract: Exposure to trichloroethylene (TCE) is linked to formation of congenital heart defects in humans and animals. Prior interactome analysis identified the transcription factor, Hepatocyte Nuclear Factor 4 alpha (HNF4a), as a potential target of TCE exposure. As a role for HNF4a is unknown in the heart, we examined developing avian hearts for HNF4a expression and for sensitivity to TCE and the HNF4a agonist, Benfluorex. In vitro analysis using a HNF4a reporter construct showed both TCE and HFN4a to be antagonists of HNF4a-mediated transcription at the concentrations tested. HNF4a mRNA is expressed transiently in the embryonic heart during valve formation and cardiac development. Embryos were examined for altered gene expression in the presence of TCE or Benfluorex. TCE altered expression of selected mRNAs including HNF4a, TRAF6 and CYP2C45. There was a transition between inhibition and induction of marker gene expression in embryos as TCE concentration increased. Benfluorex was largely inhibitory to selected markers. Echocardiography of exposed embryos showed reduced cardiac function with both TCE and Benfluorex. Cardiac contraction was reduced by 29% and 23%, respectively at 10 ppb. The effects of TCE and Benfluorex on autocrine regulation of HNF4a, selected markers and cardiac function argue for a functional interaction of TCE and HNF4a. Further, the dose-sensitive shift between inhibition and induction of marker expression may explain the nonmonotonic-like dose response observed with TCE exposure in the heart.

PubMed ID: 29306027 Exiting the NIEHS site

MeSH Terms: Animals; Chick Embryo; Dose-Response Relationship, Drug; Echocardiography; Environmental Pollutants/toxicity*; Fenfluramine/analogs & derivatives; Fenfluramine/pharmacology; Genes, Reporter; Heart/diagnostic imaging; Heart/drug effects*; Heart/embryology; Hep G2 Cells; Hepatocyte Nuclear Factor 4/agonists; Hepatocyte Nuclear Factor 4/genetics*; Humans; Myocardium/metabolism; Transcription, Genetic/drug effects*; Trichloroethylene/toxicity*

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