Activation of human mast cells by aggregated IgG through FcgammaRI: additive effects of C3a

Clin Immunol. 2004 Feb;110(2):172-80. doi: 10.1016/j.clim.2003.11.007.


Human mast cells (huMC) increase surface expression of FcgammaRI (CD64) in response to IFNgamma. Subsequent receptor aggregation of FcgammaR1 using CD64-specific F(ab')(2) or antibody directed against FcgammaR1-bound IgG results in cell activation. Human mast cells may be observed degranulating in inflammation associated with autoimmune disease and where IFNgamma is produced. We sought to determine if human mast cells cultured in IFNgamma would degranulate in response to aggregated IgG, what mediators might be generated (i.e., cytokines and eicosanoids), and whether C3a might enhance such activation. Activation of IFNgamma-treated huMC sensitized with 1 microg/ml aggregated IgG(1) resulted in 15-30% degranulation (beta-hexosaminidase release), which was half-maximal by 7.5 min; no degranulation was observed using heat-generated aggregates of IgG(2), IgG(3), or IgG(4). Activation using aggregated IgG(1) led to PGD(2) and LTC(4) generation as well as enhanced IL-3, IL-13, GM-CSF, and TNFalpha production. Preincubation of cells with F(ab')(2) from CD64-specific clone 10.1 reduced aggregated IgG(1)-mediated beta-hexosaminidase release by 38% while degranulation was unaffected by blocking FcgammaRII with F(ab')(2)-specific antibody (clone 7.3). Simultaneous activation of huMC via aggregated IgG and C3a led to additive degranulation. These data support a mechanism by which mast cells may contribute to the inflammatory component in fibrosis, vasculitis, and arthritis.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cell Degranulation / immunology
  • Complement C3a / immunology*
  • Cytokines / genetics
  • Cytokines / immunology
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Immunoglobulin G / immunology*
  • Interferon-gamma / immunology
  • Leukotriene C4 / immunology
  • Leukotriene C4 / metabolism
  • Mast Cells / cytology
  • Mast Cells / immunology*
  • Prostaglandin D2 / immunology
  • Prostaglandin D2 / metabolism
  • RNA, Messenger / chemistry
  • RNA, Messenger / genetics
  • Receptors, IgG / immunology*
  • Reverse Transcriptase Polymerase Chain Reaction
  • beta-N-Acetylhexosaminidases / immunology
  • beta-N-Acetylhexosaminidases / metabolism


  • Cytokines
  • Immunoglobulin G
  • RNA, Messenger
  • Receptors, IgG
  • Leukotriene C4
  • Complement C3a
  • Interferon-gamma
  • beta-N-Acetylhexosaminidases
  • Prostaglandin D2