Aryl hydrocarbon receptor upregulates IL-1β expression in hCMEC/D3 human cerebral microvascular endothelial cells after TCDD exposure

Toxicol In Vitro. 2017 Jun:41:200-204. doi: 10.1016/j.tiv.2017.03.001. Epub 2017 Mar 8.

Abstract

The AhR is a cytosolic ligand-dependent transcription factor activated by both endogenous and exogenous chemicals. It can regulate expression of many target genes including some inflammatory cytokines and chemokines. To date AhR implication in the regulation of inflammatory cytokines and chemokines at human cerebral endothelium has not been addressed. In the present study, we investigated whether AhR could regulate the expression of two pro-inflammatory cytokines and one chemokine i.e. IL-1β, IL-6 and IL-8 in the hCMEC/D3 human cerebral microvascular endothelial cell line. Exposure to TCDD increased IL-1β mRNA expression levels in hCMEC/D3. By using small interfering RNA against AhR we demonstrated that TCDD effects on IL-1β expression were mediated through AhR activation. Regarding IL-6 and IL-8, TCDD exposure had little or no effect on their mRNA levels in hCMEC/D3. In conclusion, our findings suggest that AhR-mediated IL-1β regulation in cerebral endothelium could induce BBB breakdown and contribute to the pathogenesis of a variety of neurologic disorders.

Keywords: Aryl hydrocarbon receptor; Blood-brain barrier; Pro-inflammatory cytokines; hCMEC/D3.

MeSH terms

  • Brain / cytology
  • Cell Line
  • Endothelial Cells / drug effects*
  • Endothelial Cells / metabolism
  • Humans
  • Interleukin-1beta / genetics*
  • Interleukin-6 / genetics
  • Interleukin-8 / genetics
  • Microvessels / cytology
  • Polychlorinated Dibenzodioxins / toxicity*
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / genetics
  • Receptors, Aryl Hydrocarbon / genetics*

Substances

  • CXCL8 protein, human
  • IL6 protein, human
  • Interleukin-1beta
  • Interleukin-6
  • Interleukin-8
  • Polychlorinated Dibenzodioxins
  • RNA, Messenger
  • RNA, Small Interfering
  • Receptors, Aryl Hydrocarbon