Dexamethasone coordinately regulates angiopoietin-1 and VEGF: a mechanism of glucocorticoid-induced stabilization of blood-brain barrier

Biochem Biophys Res Commun. 2008 Jul 18;372(1):243-8. doi: 10.1016/j.bbrc.2008.05.025. Epub 2008 May 15.

Abstract

Glucocorticoids stabilize the blood-brain barrier (BBB), leading to attenuation of vasogenic brain edema. However, the action mechanism of glucocorticoids has been poorly elucidated. To elucidate the mechanism, we investigated whether dexamethasone (Dex), a synthetic glucocorticoid hormone, regulates the levels of key permeability regulating factors such as angiopoietin-1, angiopoietin-2, and vascular endothelial growth factor (VEGF) in the three types of cells comprising BBB. Dex increased the level of angiopoietin-1 mRNA and protein and decreased VEGF mRNA and protein in brain astrocytes and pericytes, but not in endothelial cells. The mRNA and protein of angiopoietin-2 were detected only in endothelial cells and not regulated by Dex. The Dex-induced regulation of angiopoietin-1 and VEGF was inhibited by RU486, suggestive of glucocorticoid receptor mediation. The mRNA stability of angiopoietin-1 and VEGF was not changed by Dex treatment, implying that Dex increases angiopoietin-1 and decreases VEGF through transcriptional regulation. This is the first study showing the coordinate regulation of angiopoietin-1 and VEGF by glucocorticoids, suggesting a novel mechanism underlying glucocorticoids-induced stabilization of BBB.

MeSH terms

  • Angiopoietin-1 / genetics
  • Angiopoietin-1 / metabolism*
  • Blood-Brain Barrier / drug effects*
  • Blood-Brain Barrier / metabolism
  • Cell Line
  • Dexamethasone / antagonists & inhibitors
  • Dexamethasone / pharmacology*
  • Glucocorticoids / antagonists & inhibitors
  • Glucocorticoids / pharmacology*
  • Hormone Antagonists / pharmacology
  • Humans
  • Mifepristone / pharmacology
  • RNA Stability / drug effects
  • RNA, Messenger / metabolism
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor A / metabolism*

Substances

  • Angiopoietin-1
  • Glucocorticoids
  • Hormone Antagonists
  • RNA, Messenger
  • Vascular Endothelial Growth Factor A
  • Mifepristone
  • Dexamethasone