17beta-estradiol mediates protection against microvascular endothelial cell hyperpermeability

Am J Surg. 2009 Feb;197(2):147-54. doi: 10.1016/j.amjsurg.2008.10.003.

Abstract

Background: Previous work from our laboratory demonstrated the involvement of "intrinsic" mitochondrial apoptotic signaling in vascular hyperpermeability. The objective of this study was to determine if 17beta-estradiol, a known inhibitor of apoptosis, would attenuate microvascular endothelial cell hyperpermeability.

Methods: Rat lung microvascular endothelial cell monolayers were treated with 17beta-estradiol or estrogen-receptor antagonist ICI 182780 after transfection with BAK peptide (5 microg/mL). Fluorescein isothiocyanate (FITC)-albumin was used to determine the change in permeability. Mitochondrial reactive oxygen species (ROS) formation and transmembrane potential were determined using 123 dihydrorhodamine and JC-1, respectively. Cytosolic cytochrome c levels and caspase-3 activity were determined using enzyme-linked immunosorbent assay and fluorometric assay respectively.

Results: 17beta-estradiol (10 nm) attenuated BAK-induced hyperpermeability (P < .05), ROS formation, cytochrome c release, and caspase-3 activation. The estrogen receptor antagonist ICI 182780 blocked the protective effect of 17beta-estradiol on hyperpermeability (P < .05).

Conclusions: 17beta-estradiol attenuates BAK-induced hyperpermeability in rat lung microvascular endothelial cells by way of an estrogen-receptor mediated pathway.

MeSH terms

  • Animals
  • Capillary Permeability / drug effects*
  • Cardiovascular Agents / pharmacology*
  • Cells, Cultured
  • Endothelial Cells / drug effects*
  • Estradiol / pharmacology*
  • Lung / blood supply
  • Rats
  • Vascular Diseases / prevention & control*

Substances

  • Cardiovascular Agents
  • Estradiol