The principal eosinophil peroxidase product, HOSCN, is a uniquely potent phagocyte oxidant inducer of endothelial cell tissue factor activity: a potential mechanism for thrombosis in eosinophilic inflammatory states

Blood. 2006 Jan 15;107(2):558-65. doi: 10.1182/blood-2005-05-2152. Epub 2005 Sep 15.

Abstract

In vivo, bromide (Br(-)), nitrite (NO(2)(-)), and thiocyanate (SCN(-)) compete for oxidation by eosinophil peroxidase (EPO) and H(2)O(2), yielding, respectively, HOBr, NO(2)., and HOSCN. We have recently shown that SCN(-) is the strongly preferred substrate for EPO in vivo and that HOSCN, in contrast with other EPO-generated oxidants and HOCl, is a relatively weak, cell-permeant, sulfhydryl (SH)-reactive oxidant. We here show that HOSCN is a uniquely potent (up to 100-fold) phagocyte oxidant inducer of tissue factor (TF) activity in human umbilical vein endothelial cells (HUVECs). This induction is attributable to transcriptional up-regulation of TF gene expression dependent upon both activation of the p65/c-Rel TF-kappaB transcription factor and activity of the ERK1/2 kinase pathway upstream of Egr-1 and was markedly further enhanced in the presence of wortmannin, an inhibitor of the PI3 kinase/Akt pathway. HOSCN also markedly activates the proinflammatory p65/p50 NF-kappaB pathway. Based on these findings we hypothesize that HOSCN generated by adherent and infiltrating eosinophils may provoke the development of a prothrombotic and proinflammatory endothelial/endocardial phenotype that promotes the pronounced thrombotic diathesis characteristic of the hypereosinophilic syndrome.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Early Growth Response Protein 1 / metabolism
  • Electrophoretic Mobility Shift Assay
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / metabolism*
  • Eosinophil Peroxidase / metabolism
  • Eosinophils / enzymology
  • Humans
  • Lipopolysaccharides / pharmacology
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • NF-kappa B / metabolism
  • Oxidants / pharmacology*
  • Oxidation-Reduction
  • Phagocytes / cytology
  • Phagocytes / metabolism*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction*
  • Thiocyanates / pharmacology*
  • Thromboplastin / metabolism*
  • Thrombosis / immunology*
  • Thrombosis / metabolism
  • Transcription Factor AP-1 / metabolism
  • Transcription Factor RelA / genetics
  • Transcription Factor RelA / metabolism
  • Transcription, Genetic
  • Umbilical Veins / cytology
  • Umbilical Veins / metabolism
  • Up-Regulation

Substances

  • Early Growth Response Protein 1
  • Lipopolysaccharides
  • NF-kappa B
  • Oxidants
  • Thiocyanates
  • Transcription Factor AP-1
  • Transcription Factor RelA
  • Thromboplastin
  • Eosinophil Peroxidase
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3