IL-4 enhances proliferation and mediator release in mature human mast cells

Proc Natl Acad Sci U S A. 1999 Jul 6;96(14):8080-5. doi: 10.1073/pnas.96.14.8080.

Abstract

Tissue mast cells (MC) are recognized as key effector cells of immediate-type allergic reactions releasing inflammatory mediators and cytokines on stimulation with antigen, but they also might be involved in IgE-independent inflammatory and tissue repair processes. The mechanism of human MC regulation in tissue is not fully understood. Here, we show that IL-4, in synergy with stem cell factor (SCF), regulates the function of purified human MC isolated from intestinal tissue. Whereas SCF induced only marginal proliferation of MC cultured in vitro up to 4 weeks, addition of IL-4 and SCF strongly increased the proliferation rate. Moreover, IL-4, which by itself had no visible effect on human MC, enhanced the release of histamine, leukotriene C4, and IL-5 in MC triggered by IgE receptor crosslinking. The IL-4 effects occurred in a dose-dependent fashion (ED50 = 100 pg/ml) and could be totally blocked by a competitive IL-4 receptor antagonist. Our data indicate that IL-4 is an important regulator of human MC function and suggest that mature MC retain the capacity to proliferate in a particular tissue environment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Division / drug effects
  • Cells, Cultured
  • Cytokines / genetics*
  • Drug Synergism
  • Gene Expression Regulation / immunology
  • Humans
  • Interleukin-4 / pharmacology*
  • Interleukin-5 / genetics
  • Intestines / immunology
  • Kinetics
  • Leukotriene C4 / biosynthesis
  • Mast Cells / cytology
  • Mast Cells / drug effects
  • Mast Cells / immunology*
  • Recombinant Proteins / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stem Cell Factor / pharmacology
  • Time Factors
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Cytokines
  • Interleukin-5
  • Recombinant Proteins
  • Stem Cell Factor
  • Tumor Necrosis Factor-alpha
  • Interleukin-4
  • Leukotriene C4