ADAM-8, a metalloproteinase, drives acute allergen-induced airway inflammation.

نویسندگان

  • Geneviève Paulissen
  • Natacha Rocks
  • Maud M Guéders
  • Denis Bedoret
  • Céline Crahay
  • Florence Quesada-Calvo
  • Jonathan Hacha
  • Sandrine Bekaert
  • Christophe Desmet
  • Jean-Michel Foidart
  • Fabrice Bureau
  • Agnès Noel
  • Didier D Cataldo
چکیده

Asthma is a complex disease linked to various pathophysiological events including the activity of proteinases. The multifunctional A disintegrin and metalloproteinases (ADAMs) displaying the ability to cleave membrane-bound mediators or cytokines appear to be key mediators in various inflammatory processes. In the present study, we investigated ADAM-8 expression and production in a mouse model of allergen-induced airway inflammation. In allergen-exposed animals, increased expression of ADAM-8 was found in the lung parenchyma and in DC purified from the lungs. The potential role of ADAM-8 in the development of allergen-induced airway inflammation was further investigated by the use of an anti-ADAM-8 antibody and ADAM-8 knockout animals. We observed a decrease in allergen-induced acute inflammation both in BALF and the peribronchial area in anti-ADAM-8 antibody-treated mice and in ADAM-8-deficient mice (ADAM-8(-/-) ) after allergen exposure. ADAM-8 depletion led to a significant decrease of the CD11c(+) lung DC. We also report lower levels of CCL11 and CCL22 production in antibody-treated mice and ADAM-8- deficient mice that might be explained by decreased eosinophilic inflammation and lower numbers of DC, respectively. In conclusion, ADAM-8 appears to favour allergen-induced acute airway inflammation by promoting DC recruitment and CCL11 and CCL22 production.

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عنوان ژورنال:
  • European journal of immunology

دوره 41 2  شماره 

صفحات  -

تاریخ انتشار 2011