TNF-alpha induces the late-phase airway hyperresponsiveness and airway inflammation through cytosolic phospholipase A(2) activation

J Allergy Clin Immunol. 2005 Sep;116(3):537-43. doi: 10.1016/j.jaci.2005.05.034.

Abstract

Background: Late-phase airway hyperresponsiveness (AHR) in asthma is considered the event leading to persistent inflammation in the lungs, but the molecular mechanisms involved in this process are poorly understood.

Objective: To examine the role of TNF-alpha in the development of a late AHR and airway inflammation in asthma.

Methods: We established a murine model of asthma with not only biphasic AHR to methacholine but also airway eosinophilia. The effect of TNF-alpha blockade was determined by using anti-TNF-alpha antibody and TNF-alpha knockout mice. Cytosolic phospholipase A(2) (cPLA(2)) mRNA expression and activity were assessed by using RT-PCR and 1-stearoyl-2-[1-(14)C] arachidonyl-sn-glycero-3-phosphocholine as the substrate, respectively.

Results: TNF-alpha blockade resulted in significant inhibition of the late AHR without affecting the early AHR, and reduction in airway eosinophilia and inflammation. cPLA(2) activity was increased in asthmatic lungs in a TNF-alpha-dependent way, and cPLA(2) inhibitor blocked late AHR and airway eosinophilia. TNF-alpha also stimulated the synthesis of cPLA(2) metabolites such as leukotriene B(4) and platelet-activating factor in the airway. Specific inhibitors of cPLA(2) metabolites inhibited the late AHR and airway eosinophilia.

Conclusions: TNF-alpha is the proximal key cytokine capable of developing late-phase AHR and subsequent airway inflammation through expression/activation of cPLA(2).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Asthma / immunology*
  • Asthma / physiopathology
  • Bronchial Hyperreactivity / chemically induced
  • Bronchial Hyperreactivity / immunology*
  • Bronchial Hyperreactivity / physiopathology
  • Bronchoalveolar Lavage Fluid / chemistry
  • Bronchoconstrictor Agents / pharmacology
  • Cytosol / metabolism
  • Disease Models, Animal
  • Enzyme Activation / physiology
  • Histamine / immunology
  • Histamine / metabolism
  • Inflammation / immunology*
  • Leukotriene B4 / immunology
  • Leukotriene B4 / metabolism
  • Male
  • Methacholine Chloride / pharmacology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Phospholipases A / immunology
  • Phospholipases A / metabolism*
  • Platelet Activating Factor / immunology
  • Platelet Activating Factor / metabolism
  • Pulmonary Eosinophilia / immunology
  • RNA, Messenger / analysis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / immunology*

Substances

  • Bronchoconstrictor Agents
  • Platelet Activating Factor
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Methacholine Chloride
  • Leukotriene B4
  • Histamine
  • Phospholipases A