Involvement of p38 mitogen-activated protein kinase signaling pathway in osteoclastogenesis mediated by receptor activator of NF-κB ligand (RANKL)

被引:460
作者
Matsumoto, M
Sudo, T
Saito, T
Osada, A
Tsujimoto, M
机构
[1] RIKEN, Lab Cellular Biochem, Wako, Saitama 3510198, Japan
[2] RIKEN, Lab Antibiot, Wako, Saitama 3510198, Japan
关键词
D O I
10.1074/jbc.M001229200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The receptor activator of NF-kappa B ligand (RANKL) induces osteoclast differentiation from bone marrow cells in the presence of macrophage colony-stimulating factor, We found that treatment of bone marrow cells with SB203580 inhibited osteoclast differentiation via inhibition of the RANKL-mediated signaling pathway. To elucidate the role of p38 mitogen-activated protein (MAP) kinase pathway in osteoclastogenesis, we employed RAW264 cells which could differentiate into osteoclastlike cells following treatment with RANKL. In a dose-dependent manner, SB203580 but not PD98059, inhibited RANKL-induced differentiation. Among three MAP kinase families tested, this inhibition profile coincided only with the activation of p38 MAP kinase. Expression in RAW264 cells of the dominant negative form of either p38 alpha MAP kinase or MAP kinase kinase (MKK) 6 significantly inhibited RAM(L-induced differentiation of the cells, These results indicate that activation of the p38 MAP kinase pathway plays an important role in RANKL-induced osteoclast differentiation of precursor bone marrow cells.
引用
收藏
页码:31155 / 31161
页数:7
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