Intravenous Immunoglobulin (IVIG) Attenuates TNF-Induced Pathologic Bone Resorption and Suppresses Osteoclastogenesis by Inducing A20 Expression

J Cell Physiol. 2016 Feb;231(2):449-458. doi: 10.1002/jcp.25091.

Abstract

Investigations on the therapeutic effects of intravenous immunoglobulin (IVIG) have focused on the suppression of autoantibody and immune complex-mediated inflammatory pathogenesis. Inflammatory diseases such as rheumatoid arthritis are often accompanied by excessive bone erosion but the effect of IVIG on osteoclasts, bone-resorbing cells, has not been studied. Here, we investigate whether IVIG directly regulates osteoclast differentiation and has therapeutic potential for suppressing osteoclast-mediated pathologic bone resorption. IVIG or cross-linking of Fcγ receptors with plate-bound IgG suppressed receptor activator of nuclear factor-κ B ligand (RANKL)-induced osteoclastogenesis and expression of osteoclast-related genes such as integrin β3 and cathepsin K in a dose-dependent manner. Mechanistically, IVIG or plate-bound IgG suppressed osteoclastogenesis by downregulating RANKL-induced expression of NFATC1, the master regulator of osteoclastogenesis. IVIG suppressed NFATC1 expression by attenuating RANKL-induced NF-κB signaling, explained in part by induction of the inflammatory signaling inhibitor A20. IVIG administration attenuated in vivo osteoclastogenesis and suppressed bone resorption in the tumor necrosis factor (TNF)-induced calvarial osteolysis model. Our findings show that, in addition to suppressing inflammation, IVIG directly inhibits osteoclastogenesis through a mechanism involving suppression of RANK signaling. Direct suppression of osteoclast differentiation may provide beneficial effects on preserving bone mass when IVIG is used to treat rheumatic disorders.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Bone Resorption / metabolism
  • Bone Resorption / pathology
  • Bone Resorption / therapy*
  • Cell Differentiation
  • Cysteine Endopeptidases / biosynthesis*
  • Disease Models, Animal
  • Female
  • Immunoglobulins, Intravenous / therapeutic use*
  • Intracellular Signaling Peptides and Proteins / biosynthesis*
  • Mice
  • Mice, Inbred C57BL
  • NF-kappa B / metabolism
  • NFATC Transcription Factors / genetics
  • Osteoclasts / drug effects
  • Osteoclasts / metabolism
  • Osteoclasts / pathology
  • RANK Ligand / metabolism
  • Rheumatic Diseases / metabolism
  • Rheumatic Diseases / pathology
  • Rheumatic Diseases / therapy
  • Signal Transduction
  • Tumor Necrosis Factor alpha-Induced Protein 3
  • Tumor Necrosis Factor-alpha / physiology

Substances

  • Immunoglobulins, Intravenous
  • Intracellular Signaling Peptides and Proteins
  • NF-kappa B
  • NFATC Transcription Factors
  • Nfatc1 protein, mouse
  • RANK Ligand
  • Tnfsf11 protein, mouse
  • Tumor Necrosis Factor-alpha
  • Tumor Necrosis Factor alpha-Induced Protein 3
  • Cysteine Endopeptidases
  • Tnfaip3 protein, mouse