Ikeda Fumiyo, Nishimura Riko, Matsubara Takuma, Tanaka Sakae, Inoue Jun-ichiro, Reddy Sakamuri V, Hata Kenji, Yamashita Kenji, Hiraga Toru, Watanabe Toshiyuki, Kukita Toshio, Yoshioka Katsuji, Rao Anjana, Yoneda Toshiyuki
Department of Biochemistry, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka 565-0871, Japan.
J Clin Invest. 2004 Aug;114(4):475-84. doi: 10.1172/JCI19657.
Receptor activator of NF-kappaB ligand (RANKL) plays an essential role in osteoclast formation and bone resorption. Although genetic and biochemical studies indicate that RANKL regulates osteoclast differentiation by activating receptor activator of NF-kappaB and associated signaling molecules, the molecular mechanisms of RANKL-regulated osteoclast differentiation have not yet been fully established. We investigated the role of the transcription factor c-Jun, which is activated by RANKL, in osteoclastogenesis using transgenic mice expressing dominant-negative c-Jun specifically in the osteoclast lineage. We found that the transgenic mice manifested severe osteopetrosis due to impaired osteoclastogenesis. Blockade of c-Jun signaling also markedly inhibited soluble RANKL-induced osteoclast differentiation in vitro. Overexpression of nuclear factor of activated T cells 1 (NFAT1) (NFATc2/NFATp) or NFAT2 (NFATc1/NFATc) promoted differentiation of osteoclast precursor cells into tartrate-resistant acid phosphatase-positive (TRAP-positive) multinucleated osteoclast-like cells even in the absence of RANKL. Overexpression of NFAT1 also markedly transactivated the TRAP gene promoter. These osteoclastogenic activities of NFAT were abrogated by overexpression of dominant-negative c-Jun. Importantly, osteoclast differentiation and induction of NFAT2 expression by NFAT1 overexpression or soluble RANKL treatment were profoundly diminished in spleen cells of the transgenic mice. Collectively, these results indicate that c-Jun signaling in cooperation with NFAT is crucial for RANKL-regulated osteoclast differentiation.
核因子κB受体活化因子配体(RANKL)在破骨细胞形成和骨吸收过程中发挥着至关重要的作用。尽管遗传学和生物化学研究表明,RANKL通过激活核因子κB受体活化因子及相关信号分子来调节破骨细胞分化,但RANKL调节破骨细胞分化的分子机制尚未完全明确。我们利用在破骨细胞谱系中特异性表达显性负性c-Jun的转基因小鼠,研究了由RANKL激活的转录因子c-Jun在破骨细胞生成中的作用。我们发现,由于破骨细胞生成受损,转基因小鼠表现出严重的骨质硬化。阻断c-Jun信号也显著抑制了可溶性RANKL在体外诱导的破骨细胞分化。即使在没有RANKL的情况下,活化T细胞核因子1(NFAT1)(NFATc2/NFATp)或NFAT2(NFATc1/NFATc)的过表达也能促进破骨细胞前体细胞分化为抗酒石酸酸性磷酸酶阳性(TRAP阳性)的多核破骨细胞样细胞。NFAT1的过表达也显著反式激活了TRAP基因启动子。显性负性c-Jun的过表达消除了NFAT的这些破骨细胞生成活性。重要的是,在转基因小鼠的脾细胞中,NFAT1过表达或可溶性RANKL处理诱导的破骨细胞分化及NFAT2表达的诱导显著减少。总体而言,这些结果表明,c-Jun信号与NFAT协同作用对于RANKL调节的破骨细胞分化至关重要。