Cross-linking of human FcgammaRIIIb induces the production of granulocyte colony-stimulating factor and granulocyte-macrophage colony-stimulating factor by polymorphonuclear neutrophils

J Immunol. 2001 Oct 1;167(7):3996-4007. doi: 10.4049/jimmunol.167.7.3996.

Abstract

We have reported that human autoantibodies reacting with the polymorphonuclear neutrophil (PMN)-anchored FcgammaRIIIb (CD16) protect these cells from spontaneous apoptosis. In this study, we used anti-CD16 F(ab')(2) to delineate the mechanism(s) whereby the PMN life span is extended. As documented using four methods, CD16 cross-linking impeded spontaneous apoptosis, whereas anti-CD18 F(ab')(2) exerted no effect. Incubation of PMNs with anti-CD16 prevented the up-regulation of beta(2) integrins, particularly CD11b, which is the alpha-chain of complement receptor type 3, but also CD18, which is its beta-chain, as well as CD11a and CD11c. Anti-CD16-conditioned supernatant of PMNs diminished the percentage of annexin V-binding fresh PMNs after another 18 h in culture, whereas the negative control anti-CD18 had no effect. The expression of mRNA for G-CSF and GM-CSF was induced by anti-CD16, followed by the release of G-CSF and GM-CSF in a dose-dependent manner. Anti-G-CSF and anti-GM-CSF mAbs abrogated the antiapoptotic effect of the related growth factors. The delay in apoptosis was accompanied by a down-regulated expression of Bax, and a partial reduction of caspase-3 activity. These data suggest an autocrine involvement of anti-CD16-induced survival factors in the rescue of PMNs from spontaneous apoptosis. Thus, apoptosis of aged PMNs can be modulated by signaling through FcgammaRIIIb, which may occur in patients with PMN-binding anti-FcgammaRIIIb autoantibodies.

MeSH terms

  • Antibodies, Monoclonal / immunology
  • Antigens, CD / immunology
  • Antigens, CD / physiology*
  • Apoptosis*
  • Biological Factors / biosynthesis
  • CD18 Antigens / metabolism
  • Caspase 3
  • Caspases / metabolism
  • Cells, Cultured
  • Culture Media, Conditioned / pharmacology
  • GPI-Linked Proteins
  • Granulocyte Colony-Stimulating Factor / biosynthesis*
  • Granulocyte Colony-Stimulating Factor / genetics
  • Granulocyte Colony-Stimulating Factor / physiology
  • Granulocyte-Macrophage Colony-Stimulating Factor / biosynthesis*
  • Granulocyte-Macrophage Colony-Stimulating Factor / genetics
  • Granulocyte-Macrophage Colony-Stimulating Factor / physiology
  • Humans
  • Kinetics
  • Neutrophils / cytology
  • Neutrophils / immunology*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-bcl-2*
  • RNA, Messenger / biosynthesis
  • Receptors, IgG / immunology
  • Receptors, IgG / physiology*
  • Transcriptional Activation*
  • bcl-2-Associated X Protein

Substances

  • Antibodies, Monoclonal
  • Antigens, CD
  • BAX protein, human
  • Biological Factors
  • CD18 Antigens
  • Culture Media, Conditioned
  • FCGR3B protein, human
  • GPI-Linked Proteins
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Messenger
  • Receptors, IgG
  • bcl-2-Associated X Protein
  • Granulocyte Colony-Stimulating Factor
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • CASP3 protein, human
  • Caspase 3
  • Caspases