Differential effects of cytokines and corticosteroids on toll-like receptor 2 expression and activity in human airway epithelia

Respir Res. 2009 Oct 16;10(1):96. doi: 10.1186/1465-9921-10-96.

Abstract

Background: The recognition of microbial molecular patterns via toll-like receptors (TLRs) is critical for mucosal defenses.

Methods: Using well-differentiated primary cultures of human airway epithelia, we investigated the effects of exposure of the cells to cytokines (TNF-alpha and IFN-gamma) and dexamethasone (dex) on responsiveness to the TLR2/TLR1 ligand Pam3CSK4. Production of IL-8, CCL20, and airway surface liquid antimicrobial activity were used as endpoints.

Results: Microarray expression profiling in human airway epithelia revealed that first response cytokines markedly induced TLR2 expression. Real-time PCR confirmed that cytokines (TNF-alpha and IFN-gamma), dexamethasone (dex), or cytokines + dex increased TLR2 mRNA abundance. A synergistic increase was seen with cytokines + dex. To assess TLR2 function, epithelia pre-treated with cytokines +/- dex were exposed to the TLR2/TLR1 ligand Pam3CSK4 for 24 hours. While cells pre-treated with cytokines alone exhibited significantly enhanced IL-8 and CCL20 secretion following Pam3CSK4, mean IL-8 and CCL20 release decreased in Pam3CSK4 stimulated cells following cytokines + dex pre-treatment. This marked increase in inflammatory gene expression seen after treatment with cytokines followed by the TLR2 ligand did not correlate well with NF-kappaB, Stat1, or p38 MAP kinase pathway activation. Cytokines also enhanced TLR2 agonist-induced beta-defensin 2 mRNA expression and increased the antimicrobial activity of airway surface liquid. Dex blocked these effects.

Conclusion: While dex treatment enhanced TLR2 expression, co-administration of dex with cytokines inhibited airway epithelial cell responsiveness to TLR2/TLR1 ligand over cytokines alone. Enhanced functional TLR2 expression following exposure to TNF-alpha and IFN-gamma may serve as a dynamic means to amplify epithelial innate immune responses during infectious or inflammatory pulmonary diseases.

Publication types

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

MeSH terms

  • Adrenal Cortex Hormones / pharmacology*
  • Cells, Cultured
  • Chemokine CCL20 / metabolism
  • Cytokines / metabolism*
  • Dexamethasone / pharmacology*
  • Epithelial Cells / drug effects*
  • Epithelial Cells / immunology
  • Escherichia coli / immunology
  • Gene Expression Profiling / methods
  • Humans
  • Immunity, Innate / drug effects*
  • Inflammation Mediators / metabolism*
  • Interferon-gamma / metabolism
  • Interleukin-1beta / metabolism
  • Interleukin-8 / metabolism
  • Ligands
  • Lipopeptides / pharmacology
  • Listeria monocytogenes / immunology
  • Oligonucleotide Array Sequence Analysis
  • Pseudomonas aeruginosa / immunology
  • RNA, Messenger / metabolism
  • Recombinant Proteins / metabolism
  • Respiratory Mucosa / drug effects*
  • Respiratory Mucosa / immunology
  • Toll-Like Receptor 2 / drug effects*
  • Toll-Like Receptor 2 / genetics
  • Toll-Like Receptor 2 / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Adrenal Cortex Hormones
  • CCL20 protein, human
  • CXCL8 protein, human
  • Chemokine CCL20
  • Cytokines
  • Inflammation Mediators
  • Interleukin-1beta
  • Interleukin-8
  • Ligands
  • Lipopeptides
  • Pam(3)CSK(4) peptide
  • RNA, Messenger
  • Recombinant Proteins
  • TLR2 protein, human
  • Toll-Like Receptor 2
  • Tumor Necrosis Factor-alpha
  • Dexamethasone
  • Interferon-gamma