Open AccessInterleukin‐27 inhibits human osteoclastogenesis by abrogating RANKL‐mediated induction of nuclear factor of activated T cells c1 and suppressing proximal RANK signaling
Author(s) -
Kalliolias George D.,
Zhao Baohong,
Triantafyllopoulou Antigoni,
ParkMin KyungHyun,
Ivashkiv Lionel B.
Publication year - 2010
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.27200
Subject(s) - rankl , signal transduction , chemistry , microbiology and biotechnology , cancer research , interleukin , medicine , biology , cytokine , receptor , activator (genetics) , biochemistry
Objective Interleukin‐27 (IL‐27) has stimulatory and regulatory immune functions and is expressed in rheumatoid arthritis (RA) synovium. This study was undertaken to investigate the effects of IL‐27 on human osteoclastogenesis, to determine whether IL‐27 can stimulate or attenuate the osteoclast‐mediated bone resorption that is a hallmark of RA. Methods Osteoclasts were generated from blood‐derived human CD14+ cells. The effects of IL‐27 on osteoclast formation were evaluated by counting the number of tartrate‐resistant acid phosphatase–positive multinucleated cells and measuring the expression of osteoclast‐related genes. The induction of nuclear factor of activated T cells c1 (NFATc1) and the activation of signaling pathways downstream of RANK were measured by immunoblotting. The expression of key molecules implicated in osteoclastogenesis (NFATc1, RANK, costimulatory receptors, and immunoreceptor tyrosine–based activation motif–harboring adaptor proteins) was measured by real‐time reverse transcription–polymerase chain reaction. Murine osteoclast precursors obtained from mouse bone marrow and synovial fluid macrophages derived from RA patients were also tested for their responsiveness to IL‐27. Results IL‐27 inhibited human osteoclastogenesis, suppressed the induction of NFATc1, down‐regulated the expression of RANK and triggering receptor expressed on myeloid cells 2 (TREM‐2), and inhibited RANKL‐mediated activation of ERK, p38, and NF‐κB in osteoclast precursors. Synovial fluid macrophages from RA patients were refractory to the effects of IL‐27. In contrast to the findings in humans, IL‐27 only moderately suppressed murine osteoclastogenesis, and this was likely attributable to low expression of the IL‐27 receptor subunit WSX‐1 on murine osteoclast precursors. Conclusion IL‐27 inhibits human osteoclastogenesis by a direct mechanism that suppresses the responses of osteoclast precursors to RANKL. These findings suggest that, in addition to its well‐known antiinflammatory effects, IL‐27 plays a homeostatic role in restraining bone erosion. This homeostatic function is compromised under conditions of chronic inflammation such as in RA synovitis.