Primary human bone marrow adipocytes support TNF-α-induced osteoclast differentiation and function through RANKL expression

Cytokine. 2011 Dec;56(3):662-8. doi: 10.1016/j.cyto.2011.09.005. Epub 2011 Oct 1.

Abstract

Purpose: In previous reports, it was demonstrated that bone marrow adipocytes were related to steroid osteoporosis through osteoclastogenesis induced by Receptor Activator of Nuclear factor κ-B Ligand (RANKL) expression. The purpose of this study was to evaluate the effect of Tumor necrosis factor-alpha (TNF-α) on RANKL expression in bone marrow adipocytes, and osteoclast differentiation supported by human bone marrow adipocytes.

Methods: RANKL, osteoprotegerin (OPG), and macrophage-colony stimulating factor (M-CSF) mRNA expression in bone marrow adipocytes and their regulation by TNF-α treatment were measured by real-time RT-PCR. Co-cultures of bone marrow adipocytes and osteoclast precursors were performed with or without TNF-α, and osteoclast differentiation was evaluated morphologically and functionally.

Results: RANKL expression and an increase in the RANKL/OPG ratio in bone marrow adipocytes were stimulated by TNF-α treatment. In co-culture of bone marrow adipocytes and osteoclast precursors with TNF-α, the number of TRAP-positive multinuclear cells and resorption cavity formations of calcium phosphate film were increased. Osteoclast differentiation was suppressed by anti-RANKL antibody treatment. In co-culture with non-cell-contact conditions, no TRAP-positive cells or resorption cavity formations were observed.

Conclusions: TNF-α increased RANKL expression in primary human bone marrow adipocytes. TNF-α induced the ability of bone marrow adipocytes to promote osteoclast differentiation and activity in a manner directly related to RANKL expression.

MeSH terms

  • Acid Phosphatase / metabolism
  • Adipocytes / cytology*
  • Adipocytes / drug effects
  • Adipocytes / metabolism*
  • Aged
  • Aged, 80 and over
  • Bone Marrow Cells / cytology*
  • Cell Adhesion / drug effects
  • Cell Differentiation / drug effects*
  • Cell Differentiation / genetics
  • Cells, Cultured
  • Coculture Techniques
  • Female
  • Gene Expression Regulation / drug effects
  • Humans
  • Isoenzymes / metabolism
  • Male
  • Middle Aged
  • Osteoclasts / cytology*
  • Osteoclasts / drug effects
  • Osteoclasts / enzymology
  • RANK Ligand / genetics*
  • RANK Ligand / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Real-Time Polymerase Chain Reaction
  • Staining and Labeling
  • Tartrate-Resistant Acid Phosphatase
  • Time Factors
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Isoenzymes
  • RANK Ligand
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Acid Phosphatase
  • Tartrate-Resistant Acid Phosphatase