A novel subset of NK cells expressing high levels of inhibitory FcgammaRIIB modulating antibody-dependent function

J Leukoc Biol. 2008 Dec;84(6):1511-20. doi: 10.1189/jlb.0608343. Epub 2008 Aug 21.

Abstract

NK cells can kill antibody-coated target cells following engagement of FcgammaRIIIA, the major activating FcgammaR expressed by these cells. The presence of FcgammaRIIC (CD32C) has also been reported, but its contribution to the FcgammaR-dependent effector functions of NK cells remains debated. We demonstrate here that inhibitory FcgammaRIIB is also expressed by a small subset of CD56+/NKp46+ NK cells and can efficiently down-modulate their FcgammaR-dependent effector function. Immunofluorescence analyses of NK cells from 52 healthy donors showed the presence of CD56bright/FcgammaRII(-) (5.2%+/-3.4), CD56dim/FcgammaRII(lo/-) (94.1%+/-3.4), and CD56dim/FcgammaRIIbright (0.64%+/-0.72) cells. QRT-PCR and protein analyses performed on isolated FcgammaRIIbright NK cells indicated that FcgammaRIIB is strongly expressed by these cells but not by FcgammaRII(lo/-) cells. In addition, FcgammaRIIbright cells showed a weaker antibody-dependent degranulation when incubated with IgG-coated target cells compared with FcgammaRII(lo/-) NK cells, although a strong FcgammaRIIIA expression was detected in both cells. Furthermore, the addition of anti-FcgammaRII Fab paralleled a higher degranulation of FcgammaRIIbright NK cells, indicating a direct role for FcgammaRIIB in this down-modulating effect. Thus, it is proposed that FcgammaRIIBbright NK cells represent a new NK cell compartment able to down-modulate NK cell functions triggered by the engagement of activating FcgammaR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / metabolism
  • Blotting, Western
  • Cell Culture Techniques
  • Flow Cytometry
  • Fluorescent Antibody Technique
  • Humans
  • Immunoglobulin G / genetics
  • Immunoglobulin G / immunology*
  • Immunoglobulin G / metabolism*
  • Immunoprecipitation
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / metabolism*
  • Killer Cells, Natural / ultrastructure
  • Lymphocyte Subsets*
  • Phenotype
  • Receptors, IgG / genetics
  • Receptors, IgG / metabolism*

Substances

  • Antigens, CD
  • Fc gamma receptor IIB
  • Immunoglobulin G
  • Receptors, IgG