科研之友
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Background/Aims: Tuberculosis induces bone loss and activates Th1 cells that play an important role in the host defense of Bacille Calmette-Guerin tuberculosis vaccine. However, the role of tuberculosis-activated Th1 cells in differentiation of osteoclast precursors to osteoclasts is unclear. As secretion of IFN-gamma in Th1 cells is induced by tuberculosis, we aimed to investigate the role of anti-IFN-gamma antibody on the differentiation and activation of osteoclasts in bone marrow monocyte-derived macrophages (BMMs). Methods: BMMs were isolated and co-cultured with CD4+T helper 1 cells (Th1 cells), pretreated with anti-IFN-gamma antibody. Then, cell proliferation, expression and release of cytokines, formation of actin ring, differentiation of osteoclasts and bone resorption function were measured by CCK8 assay, qRT-PCR/Western blot/flow cytometry, ELISA, immunofluorescence, tartrate-resistant acidic phosphatase (TRAP) staining and bone absorbance assay, respectively. Results: Anti-IFN-gamma antibody inhibited the cell viability of BMMs, and induced the expressions of RANKL, TNF-alpha, NF-kappa B and TRAF6 in BMMs. In addition, it led to increased expression levels of RANK on cell surfaces, and increased production of RANKL, TNF-alpha, MCP-1 and SDF-1. Anti-IFN-gamma antibody also induced the expression of osteoclast differentiation factor and actin ring formation, but inhibited the expression of osteoprotegerin. TRAP staining and bone resorption assays showed that anti-IFN-gamma antibody induced an increase in osteoclast formation and bone resorption. Conclusion: The anti-IFN-gamma antibody induced osteoclast formation, and is probably mediated by RANKL-induced activation of NF-kappa B, that induces TRAF6 in the RANKL-RANK signaling pathway. Our data suggest an inhibitory role for IFN-gamma in osteoclast formation induced by tuberculosis.
- 出版日期2018
