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- W2029523356 abstract "TNF-α plays critical roles in bone-resorbing diseases, such as rheumatoid arthritis. Recent evidence suggests that thiazolidinediones (TZDs), which are peroxisome proliferator-activated receptor γ agonists, have anti-inflammatory effects. The aim of this study was to evaluate the effect of TZDs on the TNF-α-mediated osteoclastogenesis of osteoclast precursor cells. TNF-α treatment of RAW264.7 murine macrophages or mouse bone marrow cells induced significant multinuclear osteoclast formation, and these differentiated osteoclast cells possessed bone-resorbing activity. The TZD drugs, rosiglitazone and pioglitazone, significantly inhibited TNF-α-induced osteoclast differentiation from both cell types and subsequent bone resorption. Reverse transcriptase-polymerase chain reaction, reporter gene assays, and Western blot results revealed that TZD treatment significantly suppressed NFATc1 expression. Moreover, GW9662 (a peroxisome proliferator-activated receptor γ antagonist) prevented the inhibitory effect of TZDs on NFATc1 expression and osteoclast differentiation. In summary, our results demonstrate that TZDs inhibit TNF-α-mediated osteoclast differentiation by downregulation of NFATc1 expression. This observation increases the therapeutic applications of TZDs in inflammatory bone-resorbing diseases." @default.
- W2029523356 created "2016-06-24" @default.
- W2029523356 creator A5001793326 @default.
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- W2029523356 date "2010-06-01" @default.
- W2029523356 modified "2023-10-16" @default.
- W2029523356 title "THIAZOLIDINEDIONES INHIBIT TNF-α-MEDIATED OSTEOCLAST DIFFERENTIATION OF RAW264.7 MACROPHAGES AND MOUSE BONE MARROW CELLS THROUGH DOWNREGULATION OF NFATc1" @default.
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- W2029523356 doi "https://doi.org/10.1097/shk.0b013e3181cc0738" @default.
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