Proteases induce production of thymic stromal lymphopoietin by airway epithelial cells through protease-activated receptor-2

J Immunol. 2009 Jul 15;183(2):1427-34. doi: 10.4049/jimmunol.0900904. Epub 2009 Jun 26.

Abstract

Thymic stromal lymphopoietin (TSLP) is produced by epithelial cells and triggers dendritic cell-mediated Th2-type inflammation. Although TSLP is up-regulated in epithelium of patients with asthma, the factors that control TSLP production have not been studied extensively. Because mouse models suggest roles for protease(s) in Th2-type immune responses, we hypothesized that proteases from airborne allergens may induce TSLP production in a human airway epithelial cell line, BEAS-2B. TSLP mRNA and protein were induced when BEAS-2B cells were exposed to prototypic proteases, namely, trypsin and papain. TSLP induction by trypsin required intact protease activity and also a protease-sensing G protein-coupled receptor, protease-activated receptor (PAR)-2; TSLP induction by papain was partially dependent on PAR-2. In humans, exposure to ubiquitous airborne fungi, such as Alternaria, is implicated in the development and exacerbation of asthma. When BEAS-2B cells or normal human bronchial epithelial cells were exposed to Alternaria extract, TSLP was potently induced. The TSLP-inducing activity of Alternaria was partially blocked by treating the extract with a cysteine protease inhibitor, E-64, or by infecting BEAS-2B cells with small interfering RNA for PAR-2. Protease-induced TSLP production by BEAS-2B cells was enhanced synergistically by IL-4 and abolished by IFN-gamma. These findings demonstrate that TSLP expression is induced in airway epithelial cells by exposure to allergen-derived proteases and that PAR-2 is involved in the process. By promoting TSLP production in the airways, proteases associated with airborne allergens may facilitate the development and/or exacerbation of Th2-type airway inflammation, particularly in allergic individuals.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allergens / pharmacology
  • Cell Line
  • Cytokines / biosynthesis*
  • Cytokines / genetics
  • Epithelial Cells / metabolism*
  • Humans
  • Papain / pharmacology
  • Peptide Hydrolases / pharmacology*
  • RNA, Messenger / biosynthesis
  • Receptor, PAR-2 / physiology*
  • Respiratory System / cytology
  • Respiratory System / metabolism*
  • Thymic Stromal Lymphopoietin
  • Transcriptional Activation*
  • Trypsin / pharmacology

Substances

  • Allergens
  • Cytokines
  • RNA, Messenger
  • Receptor, PAR-2
  • Peptide Hydrolases
  • Trypsin
  • Papain
  • Thymic Stromal Lymphopoietin