Histamine differentially interacts with tumor necrosis factor-alpha and thrombin in endothelial tissue factor induction: the role of c-Jun NH2-terminal kinase

J Thromb Haemost. 2006 Nov;4(11):2452-60. doi: 10.1111/j.1538-7836.2006.02175.x. Epub 2006 Aug 25.

Abstract

Background: Histamine plays an important role in vascular disease. Tissue factor (TF) expression is induced in vascular inflammation and acute coronary syndromes.

Objectives: This study examined the effect of histamine on tumor necrosis factor-alpha- (TNF-alpha-) vs. thrombin-induced endothelial TF expression.

Methods and results: Histamine (10(-8)-10(-5) mol L-1), TNF-alpha (5 ng mL-1), and thrombin (1 U mL-1) induced TF expression in human endothelial cells. Although TF expression by TNF-alpha and thrombin was identical, histamine augmented TNF-alpha-induced expression 7.0-fold, but thrombin-induced expression only 2.6-fold. Similar responses occurred with TF activity. The H1-receptor antagonist mepyramine abrogated these effects. Differential augmentation by histamine was also observed at the mRNA level. Histamine-induced p38 activation preceded a weak second activation to both TNF-alpha and thrombin. Histamine-induced c-Jun NH2-terminal kinase (JNK) activation was followed by a strong second activation to TNF-alpha, and less to thrombin. Selective inhibition of this second JNK activation by SP600125 reduced TF induction to histamine plus TNF-alpha by 67%, but to histamine plus thrombin by only 32%. Histamine augmented TNF-alpha- and thrombin-induced vascular cell adhesion molecule 1 (VCAM-1) expression to a similar extent. Consistent with this observation, VCAM-1 induction to TNF-alpha and thrombin was mediated by p38, but not by JNK.

Conclusions: Histamine differentially augments TNF-alpha- vs. thrombin-induced TF expression and activity, which is mediated by the H1-receptor, occurs at the mRNA level, and is related to differential JNK activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Anthracenes / pharmacology
  • Cell Adhesion / drug effects
  • Cells, Cultured
  • Coronary Disease / metabolism*
  • Endothelial Cells / metabolism
  • Endothelial Cells / pathology
  • Enzyme Activation / drug effects
  • Gene Expression Regulation / drug effects
  • Hemostatics / pharmacology*
  • Histamine / pharmacology*
  • Humans
  • JNK Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • JNK Mitogen-Activated Protein Kinases / metabolism*
  • Receptors, Histamine H1 / metabolism
  • Signal Transduction / drug effects
  • Syndrome
  • Thrombin / pharmacology*
  • Thromboplastin / biosynthesis*
  • Tumor Necrosis Factor-alpha / pharmacology*
  • Vascular Cell Adhesion Molecule-1 / biosynthesis
  • Vasculitis / metabolism*

Substances

  • Anthracenes
  • Hemostatics
  • Receptors, Histamine H1
  • Tumor Necrosis Factor-alpha
  • Vascular Cell Adhesion Molecule-1
  • pyrazolanthrone
  • Histamine
  • Thromboplastin
  • JNK Mitogen-Activated Protein Kinases
  • Thrombin