Hasegawa Tomokazu, Yoshimura Yoshitaka, Kikuiri Takashi, Yawaka Yasutaka, Takeyama Sadaaki, Matsumoto Akira, Oguchi Haruhisa, Shirakawa Tetsuo
Department of Pediatric Dentistry, School of Dentistry, Hokkaido University, Sapporo, Hokkaido, Japan.
J Periodontal Res. 2002 Dec;37(6):405-11. doi: 10.1034/j.1600-0765.2002.01603.x.
The receptor activator of NF-kappa B ligand (RANKL) and its decoy receptor, osteoprotegerin (OPG), are the important proteins implicated in osteoclastogenesis. In this study, we investigated the expressions of RANKL and OPG in cultured human periodontal ligament (PDL) cells and their roles in osteoclastogenesis. Northern blotting revealed that the OPG mRNA was down-regulated remarkably by application of 10-8 m one-alpha, 25-dihydroxyvitamin D3[1,25-(OH)2D3] and 10-7 m dexamethasone (Dex). In contrast, RANKL mRNA was up-regulated by the same treatment. Western blotting demonstrated decrease of OPG by the application of 1,25-(OH)2D3 and Dex. Tartrate-resistant acid phosphatase-positive multinuclear cells were markedly induced when the PDL cells were cocultured with mouse bone marrow cells in the presence of an anti-OPG antibody together with 1,25-(OH)2D3 and Dex. These results indicate that PDL cells synthesize both RANKL and OPG and that inactivation of OPG may play a key role in the differentiation of osteoclasts.
核因子κB受体活化因子配体(RANKL)及其诱饵受体骨保护素(OPG)是破骨细胞生成过程中涉及的重要蛋白质。在本研究中,我们调查了RANKL和OPG在培养的人牙周膜(PDL)细胞中的表达及其在破骨细胞生成中的作用。Northern印迹分析显示,应用10^-8 mol/L 1,25-二羟维生素D3[1,25-(OH)2D3]和10^-7 mol/L地塞米松(Dex)可显著下调OPG mRNA。相反,相同处理可上调RANKL mRNA。Western印迹分析表明,应用1,25-(OH)2D3和Dex可使OPG减少。当PDL细胞与小鼠骨髓细胞在抗OPG抗体存在的情况下,同时加入1,25-(OH)2D3和Dex共同培养时,可明显诱导抗酒石酸酸性磷酸酶阳性多核细胞的形成。这些结果表明,PDL细胞可同时合成RANKL和OPG,且OPG的失活可能在破骨细胞分化中起关键作用。