Modulation of antigenic phenotype in cultured human osteoblast-like cells by FGFb, TGFbeta1, PDGF-BB, IL-2, IL-1beta, LPS and IFNgamma

Biosci Rep. 2006 Aug;26(4):281-9. doi: 10.1007/s10540-006-9022-z.

Abstract

Background/aims: Recent reports demonstrated that osteoblast-like cells can also exert activities directly associated with the immune system (cytokine synthesis, antigen presentation, phagocytosis and stimulation of T lymphocytes). The present study aimed to analyze the effect of Transforming growth factorbeta1 (TGFbeta1), Fibroblast growth factor basic (FGFb), Platelet-derived growth factor-BB (PDGF-BB), Interleukin-1beta (IL-1beta), Interleukin-2 (IL-2), Lipopolysaccharide (LPS) and Interferon-gamma (IFNgamma) on the expression on osteoblast-like cells of antigens involved in antigen presentation.

Methods: Flow cytometry was used to investigate whether the growth factors FGFb, TGFbeta1, PDGF-BB, IL-2, IL-1beta, LPS and IFNgamma modulate the expression on cultured human osteoblast-like cells of different antigens involved in antigen-presentation and T cell activation.

Results: TGFbeta1 treatment significantly reduced the expression of CD54 and CD86. IL-1beta treatment significantly enhanced the expression of CD54, CD86 and HLA-DR. LPS and IFNgamma treatments produced a major increase in CD54, CD80, CD86 and HLA-DR expression. Expression of these antigen-presenting molecules was not significantly modified by FGFb, PDGF-BB or IL-2 treatment.

MeSH terms

  • Adult
  • Antigens, CD / metabolism
  • B7-1 Antigen / metabolism
  • B7-2 Antigen / metabolism
  • Becaplermin
  • Cells, Cultured
  • Cytokines / pharmacology*
  • Female
  • Fibroblast Growth Factor 2 / pharmacology
  • Flow Cytometry
  • HLA-DR Antigens / metabolism
  • Humans
  • Intercellular Adhesion Molecule-1 / metabolism
  • Interferon-gamma / pharmacology*
  • Interleukin-1beta / pharmacology*
  • Interleukin-2 / pharmacology
  • Lipopolysaccharides / pharmacology*
  • Male
  • Osteoblasts / cytology
  • Osteoblasts / drug effects*
  • Osteoblasts / metabolism
  • Platelet-Derived Growth Factor / pharmacology
  • Proto-Oncogene Proteins c-sis
  • Transforming Growth Factor beta1 / pharmacology*

Substances

  • Antigens, CD
  • B7-1 Antigen
  • B7-2 Antigen
  • Cytokines
  • HLA-DR Antigens
  • Interleukin-1beta
  • Interleukin-2
  • Lipopolysaccharides
  • Platelet-Derived Growth Factor
  • Proto-Oncogene Proteins c-sis
  • Transforming Growth Factor beta1
  • Fibroblast Growth Factor 2
  • Intercellular Adhesion Molecule-1
  • Becaplermin
  • Interferon-gamma