House dust mite, Dermatophagoides pteronissinus increases expression of MCP-1, IL-6, and IL-8 in human monocytic THP-1 cells

Cytokine. 2008 Jun;42(3):365-71. doi: 10.1016/j.cyto.2008.03.010. Epub 2008 May 19.

Abstract

The house dust mite (Dermatophagoides pteronissinus) plays an important role in the pathogenesis of allergic diseases, including atopic dermatitis, and asthma. Monocyte chemotactic protein 1 (MCP-1/CCL2)/IL-6/IL-8 (CXCL8) plays a pivotal role in mediating the infiltration of various cells into the skin of atopic dermatitis and psoriasis. The aim of this study was to investigate the effect of D. pteronissinus extract (DpE) on expression of MCP-1/IL-6/IL-8 mRNA and protein and the signal transduction in the human monocytic cell line, THP-1. The mRNA and protein expression of MCP-1/CCL2, IL-6, and IL-8 were elevated by DpE in a time and dose-dependent manner in THP-1 cells. The increased expression of MCP-1, IL-6, and IL-8 was not affected by aprotinin (serine protease inhibitor) or E64 (cysteine protease inhibitor). We found that MCP-1 and IL-6 expression due to DpE was related to Src, protein kinase C delta (PKC delta), extracellular-signal-regulated kinase (ERK) and p38 mitogen-activated protein kinase (MAPK) and IL-8 expression was involved in Src family tyrosine kinase, PKC delta, ERK. DpE increased the phosphorylation of ERK and p38 MAPK after 5min and peaked at 30min. The activation was significantly blocked by PP2, an inhibitor of Src family tyrosine kinase and rottlerin, an inhibitor of PKC delta (p<0.01). DpE increases MCP-1, IL-6, and IL-8 expression and transduces its signal via Src family tyrosine kinase, PKC, and ERK in a protease-independent manner. This finding may contribute to the elucidation of the pathogenic mechanism triggered by DpE .

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetophenones / pharmacology
  • Allergens / immunology*
  • Animals
  • Antigens, Dermatophagoides / immunology*
  • Benzopyrans / pharmacology
  • Cell Line
  • Chemokine CCL2 / biosynthesis
  • Cysteine Proteinase Inhibitors / pharmacology
  • Dermatophagoides pteronyssinus / immunology*
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Humans
  • Interleukin-6 / biosynthesis
  • Interleukin-8 / biosynthesis
  • Monocytes / drug effects
  • Monocytes / metabolism*
  • Phosphorylation
  • Protein Kinase C-delta / metabolism
  • Pyrimidines / pharmacology
  • RNA, Messenger / analysis
  • Serine Proteinase Inhibitors / pharmacology
  • Signal Transduction*
  • Time Factors
  • p38 Mitogen-Activated Protein Kinases / metabolism
  • src-Family Kinases / metabolism

Substances

  • AG 1879
  • Acetophenones
  • Allergens
  • Antigens, Dermatophagoides
  • Benzopyrans
  • CCL2 protein, human
  • CXCL8 protein, human
  • Chemokine CCL2
  • Cysteine Proteinase Inhibitors
  • IL6 protein, human
  • Interleukin-6
  • Interleukin-8
  • Pyrimidines
  • RNA, Messenger
  • Serine Proteinase Inhibitors
  • rottlerin
  • src-Family Kinases
  • Protein Kinase C-delta
  • Extracellular Signal-Regulated MAP Kinases
  • p38 Mitogen-Activated Protein Kinases