Montelukast regulates eosinophil protease activity through a leukotriene-independent mechanism

J Allergy Clin Immunol. 2006 Jul;118(1):113-9. doi: 10.1016/j.jaci.2006.03.010. Epub 2006 May 19.

Abstract

Background: Migration of eosinophils into bronchial mucosa requires proteolysis. Montelukast, a cysteinyl leukotriene (CysLT) 1 receptor antagonist used in asthma treatment, decreases eosinophil infiltration into the asthmatic airways, suggesting that CysLTs modulate eosinophil protease activity.

Objective: We sought to determine whether CysLTs and montelukast regulate eosinophil protease activity.

Methods: Purified blood eosinophils were treated with or without montelukast; MK-0591, a 5-lipoxygenase-activating protein inhibitor; or leukotriene (LT) D(4). Migration assays through Matrigel were performed in the presence of 5-oxo-6,8,11,14-eicosatetraenoic acid (5-oxo-ETE), a potent eosinophil chemotactic factor, or LTD(4). Expression of molecules implicated in plasmin generation and matrix metalloproteinase (MMP) 9 release were also evaluated.

Results: Montelukast and MK-0591 decreased eosinophil migration promoted by 5-oxo-ETE, whereas LTD(4) failed to induce eosinophil migration. However, LTD(4) significantly boosted the migration rate obtained with a suboptimal concentration of 5-oxo-ETE and partially reversed the inhibition obtained with MK-0591. Montelukast significantly reduced the maximal rate of activation of plasminogen into plasmin by eosinophils obtained with 5-oxo-ETE. 5-Oxo-ETE increased the number of eosinophils expressing urokinase plasminogen activator receptor and stimulated secretion of MMP-9. Montelukast, but neither MK-0591 nor LTD(4), reduced the expression of urokinase plasminogen activator receptor and the secretion of MMP-9 and increased total cellular activity of urokinase plasminogen activator and the expression of plasminogen activator inhibitor 2 mRNA.

Conclusion: Montelukast inhibits eosinophil protease activity in vitro through a mechanism that might be independent of its antagonist effect on CysLT 1 receptor.

Clinical implications: This could partially explain montelukast's anti-inflammatory effect in asthma and eventually amplify to improve its therapeutic efficacy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetates / pharmacology*
  • Adult
  • Arachidonic Acids / pharmacology
  • Cell Movement / drug effects
  • Cyclopropanes
  • Cysteine / physiology*
  • Enzyme Activation
  • Eosinophils / drug effects*
  • Eosinophils / enzymology
  • Eosinophils / physiology
  • Female
  • Humans
  • Indoles / pharmacology
  • Leukotriene Antagonists / pharmacology*
  • Leukotrienes / physiology*
  • Male
  • Matrix Metalloproteinase 9 / metabolism
  • Quinolines / pharmacology*
  • Receptors, Cell Surface / analysis
  • Receptors, Urokinase Plasminogen Activator
  • Sulfides
  • Urokinase-Type Plasminogen Activator / metabolism

Substances

  • Acetates
  • Arachidonic Acids
  • Cyclopropanes
  • Indoles
  • Leukotriene Antagonists
  • Leukotrienes
  • PLAUR protein, human
  • Quinolines
  • Receptors, Cell Surface
  • Receptors, Urokinase Plasminogen Activator
  • Sulfides
  • cysteinyl-leukotriene
  • 5-oxo-6,8,11,14-eicosatetraenoic acid
  • MK 0591
  • Urokinase-Type Plasminogen Activator
  • Matrix Metalloproteinase 9
  • Cysteine
  • montelukast