Essential role of p38 mitogen-activated protein kinase in contact hypersensitivity

J Biol Chem. 2002 Oct 4;277(40):37896-903. doi: 10.1074/jbc.M207326200. Epub 2002 Jul 22.

Abstract

The present study was designed to elucidate the role of p38 mitogen-activated protein kinase (p38) in the pathogenesis of inflammation, using a mouse contact hypersensitivity (CHS) model induced by 2,4-dinitro-1-fluorobenzene (DNFB). Ear swelling was induced by challenge with DNFB, accompanied by infiltration of mononuclear cells, neutrophils, and eosinophils and a marked increase in mRNA levels of cytokines such as interleukin (IL)-2, interferon (IFN)-gamma, IL-4, IL-5, IL-1beta, IL-18, and tumor necrosis factor-alpha in the challenged ear skin. Both ear swelling and the number of infiltrated cells in DNFB-challenged ear skin were significantly inhibited by treatment with SB202190, a p38 inhibitor. Furthermore, the DNFB-induced expression of all cytokines except IL-4 was significantly inhibited by treatment with SB202190. Ribonuclease protection assay revealed that the mRNA levels of chemokines such as IP-10 and MCP-1 in ear skin were markedly increased at 24 h after challenge with DNFB. The induction of these chemokines was significantly inhibited by treatment with SB202190. In p38alpha +/- mice, both ear swelling and infiltration of cells induced by DNFB were reduced compared with those in wild-type mice. However, induction of cytokines by DNFB was also observed in p38alpha +/- mice, although the induction of IFN-gamma, IL-5, and IL-18 was typically reduced compared with that in wild-type mice. Challenge with DNFB slightly induced IP-10 and MCP-1 mRNA in p38alpha +/- mice, with weaker signals than those in SB202190-treated wild-type mice. These results suggest that p38 plays a key role in CHS and is an important target for the treatment of CHS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allergens
  • Animals
  • Base Sequence
  • DNA Primers
  • Dermatitis, Contact / enzymology*
  • Dinitrofluorobenzene
  • Disease Models, Animal
  • Enzyme Inhibitors / pharmacology
  • Female
  • Imidazoles / pharmacology
  • Inflammation
  • Kinetics
  • Mice
  • Mitogen-Activated Protein Kinases / immunology*
  • Mitogen-Activated Protein Kinases / metabolism*
  • Polymerase Chain Reaction
  • Pyridines / pharmacology
  • Skin / enzymology
  • Skin / pathology*
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Allergens
  • DNA Primers
  • Enzyme Inhibitors
  • Imidazoles
  • Pyridines
  • Dinitrofluorobenzene
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole