Differential contribution of osteoclast- and osteoblast-lineage cells to CpG-oligodeoxynucleotide (CpG-ODN) modulation of osteoclastogenesis

J Bone Miner Res. 2005 Sep;20(9):1692-9. doi: 10.1359/JBMR.050515. Epub 2005 May 23.

Abstract

CpG-ODNs modulate osteoclast differentiation through Toll-like receptor 9 (TLR9). Using TLR9-deficient mice, we found that activation of TLR9 on both osteoclast precursors and osteoblasts mediate the osteoclastogenic effect of CpG-ODN. Osteoclastic TLR9 is more important for this activity.

Introduction: Bacterial infections cause pathological bone loss by accelerating differentiation and activation of the osteoclast. A variety of bacteria-derived molecules have been shown to enhance osteoclast differentiation through activation of Toll-like receptors (TLRs). We have shown that CpG-oligodeoxynucleotides (CpG-ODNs), mimicking bacterial DNA and exerting their cellular activities through TLR9, modulate osteoclast differentiation in a complex manner: the ODNs inhibit the activity of the physiological osteoclast differentiation factor RANKL in early osteoclast precursors (OCPs) but markedly stimulate osteoclastogenesis in cells primed by RANKL.

Materials and methods: Osteoclast precursors and osteoblasts from TLR9-deficient (TLR9-/-) and wildtype (TLR9+/+) mice were used for in vitro analyses of osteoclast differentiation and modulation of signal transduction and gene expression.

Results: As expected CpG-ODN did not exert any activity in cells derived from TLR9-/-mice; these cells, however, responded in a normal manner to other stimuli. Using bone marrow/osteoblasts co-cultures from all possible combinations of TLR9-/- and TLR9+/+ mice-derived cells, we showed that TLR9 in the two lineages is required for CpG-ODN induction of osteoclastogenesis.

Conclusions: CpG-ODN modulates osteoclastogenesis in a TLR9-dependent manner. Activation of TLR9 in bone marrow-derived osteoclasts precursors is more crucial to induction of osteoclastogenesis than activation of the osteoblastic TLR9.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Northern
  • Blotting, Western
  • Bone Marrow Cells / cytology*
  • Carrier Proteins / biosynthesis
  • Cell Differentiation
  • Cell Lineage
  • Coculture Techniques
  • CpG Islands
  • Culture Media, Serum-Free / pharmacology
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation*
  • Macrophages / cytology
  • Membrane Glycoproteins / biosynthesis
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Oligodeoxyribonucleotides / pharmacology*
  • Osteoblasts / cytology*
  • Osteoblasts / metabolism
  • Osteoclasts / cytology*
  • Phosphorylation
  • RANK Ligand
  • Receptor Activator of Nuclear Factor-kappa B
  • Time Factors
  • Toll-Like Receptor 9 / genetics
  • Toll-Like Receptor 9 / physiology*
  • Tumor Necrosis Factor-alpha / biosynthesis
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • CPG-oligonucleotide
  • Carrier Proteins
  • Culture Media, Serum-Free
  • Membrane Glycoproteins
  • Oligodeoxyribonucleotides
  • RANK Ligand
  • Receptor Activator of Nuclear Factor-kappa B
  • Tnfrsf11a protein, mouse
  • Tnfsf11 protein, mouse
  • Toll-Like Receptor 9
  • Tumor Necrosis Factor-alpha
  • p38 Mitogen-Activated Protein Kinases