Interleukin-4 induces activation of mitogen-activated protein kinase and phosphorylation of shc in human keratinocytes

J Biol Chem. 1996 Apr 12;271(15):8529-32. doi: 10.1074/jbc.271.15.8529.

Abstract

Most cytokines stimulate the p21ras pathway, leading to MAP kinase activation. One exception is interleukin-4 (IL-4), which has been shown not to activate this pathway in hematopoietic cells. However, IL-4 acts on a broad range of cells, including keratinocytes, in which it induces IL-6 production. We report here that IL-4 stimulation of human keratinocytic cell lines or primary cultures activates MAP kinase. In these cells, IL-4 stimulation induces the tyrosine phosphorylation of p42/44 MAP kinase as well as its catalytic activity. We also observed an increased phosphorylation of p46shc, an SH2-containing protein involved in the Ras pathway, as a result of IL-4 stimulation in human keratinocytic cell lines but not in T lymphocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing*
  • Adaptor Proteins, Vesicular Transport*
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism*
  • Cells, Cultured
  • Humans
  • Interleukin-4 / pharmacology*
  • Keratinocytes / metabolism
  • Lymphocyte Activation
  • Phosphorylation
  • Phosphotyrosine / metabolism*
  • Proteins / metabolism*
  • Recombinant Proteins
  • Shc Signaling Adaptor Proteins
  • Signal Transduction
  • Src Homology 2 Domain-Containing, Transforming Protein 1
  • T-Lymphocytes / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Adaptor Proteins, Vesicular Transport
  • Proteins
  • Recombinant Proteins
  • SHC1 protein, human
  • Shc Signaling Adaptor Proteins
  • Src Homology 2 Domain-Containing, Transforming Protein 1
  • Interleukin-4
  • Phosphotyrosine
  • Calcium-Calmodulin-Dependent Protein Kinases