Chen Zhan-kun, Lv Hou-shan, Jiang Jun
Arthritis Clinic & Research Center, Peking University People's Hospital, Beijing, China.
Artif Cells Blood Substit Immobil Biotechnol. 2010;38(1):52-6. doi: 10.3109/10731190903495785.
Our previous study showed that Leukotriene B4 can directly stimulate osteoclast differentiation independent of RANKL. In order to determine whether Leukotriene B4 could indirectly stimulate human osteoclast differentiation through increasing RANKL expression of rheumatoid arthritis fibroblast-like synoviocytes, we utilize the coculture model of rheumatoid arthritis fibroblast-like synoviocytes and monocyte, which were stimulated in the presence of 2.5 ng/ml M-CSF in the control group, 2.5 ng/ml M-CSF+10(-8)M LTB4 in the experimental group a, and 2.5 ng/ml M-CSF+10(-8)M LTB4+100 ng/ml OPG in the experimental group b. After culture for 3 weeks, the number of multinucleated TRAP staining positive osteoclast-like cells stained with TRAP was counted to evaluate the differentiation effect in each group. There was almost no osteoclast-like cell in the control group and the experimental group b. There were many osteoclast-like cells in the experimental group a. These results indicated that Leukotriene B4 is capable of inducing osteoclast differentiation by a RANKL-dependent mechanism.
我们之前的研究表明,白三烯B4可独立于核因子κB受体活化因子配体(RANKL)直接刺激破骨细胞分化。为了确定白三烯B4是否可通过增加类风湿关节炎成纤维样滑膜细胞的RANKL表达来间接刺激人破骨细胞分化,我们采用了类风湿关节炎成纤维样滑膜细胞与单核细胞的共培养模型,对照组在2.5 ng/ml巨噬细胞集落刺激因子(M-CSF)存在的情况下进行刺激,实验组a在2.5 ng/ml M-CSF + 10(-8)M白三烯B4存在的情况下进行刺激,实验组b在2.5 ng/ml M-CSF + 10(-8)M白三烯B4 + 100 ng/ml骨保护素(OPG)存在的情况下进行刺激。培养3周后,对用抗酒石酸酸性磷酸酶(TRAP)染色的多核TRAP染色阳性破骨细胞样细胞数量进行计数,以评估每组的分化效果。对照组和实验组b中几乎没有破骨细胞样细胞。实验组a中有许多破骨细胞样细胞。这些结果表明,白三烯B4能够通过RANKL依赖性机制诱导破骨细胞分化。