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Effect of recombinant TRAIL in a murine co-culture system of osteoclastogenesis

机译:重组TRAIL在小鼠破骨细胞共培养系统中的作用

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摘要

Although some experimental evidence has implicated the TRAIL/TRAIL-receptor system in the regulation of osteoclastogenesis, the only available studies performed so far have been performed on isolated pre-osteoclasts, induced to differentiate by the addition of recombinant RANKL and M-CSF Using a more physiological co-culture system in the absence of exogenous cytokines, we have here demonstrated that recombinant TRAIL inhibits osteoclast formation, but only at relatively high concentrations (500 ng/mL).
机译:尽管一些实验证据表明TRAIL / TRAIL受体系统参与破骨细胞生成的调控,但迄今为止,仅有的研究仅针对分离的破骨细胞,通过添加重组RANKL和M-CSF诱导分化。在没有外源细胞因子的情况下,在更多的生理共培养系统中,我们证明了重组TRAIL可以抑制破骨细胞的形成,但只能在相对较高的浓度(500 ng / mL)下进行。

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