Huang Peng, Wang Yan, Chi Zhi-yong, Yang Zi-yi, Ni Jian, Yang Wu-jian, Wang Ran-dong, Bai Jin-zhu
Department of Orthopaedic Surgery, People's Liberation Army General Hospital, Beijing 100853, China.
Zhonghua Wai Ke Za Zhi. 2005 Jun 15;43(12):812-6.
To study the effect of combination rhOPG-Fc and alendronate on mature osteoclasts.
Recombinant human osteoprotegerin secretory expression in P. pastoris was performed. Osteoblasts were got from new born mouse skeletal bone and proved by ALP staining and incubated together with osteoclasts precursor cell line Raw 264.7 in 96 well plate. After 9 d, 10 micromol/L ALN, 10(-5) g/L rhOPG-Fc, 10 micromol/L ALN + 10(-5) g/L rhOPG-Fc, 5 micromol/L ALN + 5 x 10(-6) g/L rhOPG-Fc were added to these coculture systems. Osteoblasts cultured without the drugs mentioned above served as controls. TRAP stain positive cells counting and cortical bone pit formation counting were preformed in the following the 3rd and 7th d.
SDS-PAGE and Western blot showed that molecular weight of the expressed protein was about 55 KD, and it could reach specifically with anti-IgG antibody. Many multi-nuclear TRAP stain positive cells were found in the coculture control group after 9 d incubation, and proved to be mature osteoclasts by TRAP stain. In the 3rd and 7th d after the addition of rhOPG-Fc, ALN or both, TRAP stain positive cells counting and cortical bone pit formation counting decreased significantly in the rhOPG-Fc, ALN or both groups than in the control group, and the combine group (10(-5) g/L rhOPG-Fc + 10 micromol/L ALN) decreased most significantly when compared with rhopG-FC or ALN single.
rhOPG-Fc can decrease the number of osteoclasts and inhibit their function. The combination of both rhOPG-Fc and ALN shows the significant inhibition effect on mature osteoclasts.
研究重组人骨保护素(rhOPG-Fc)与阿仑膦酸钠联合应用对成熟破骨细胞的影响。
进行重组人骨保护素在毕赤酵母中的分泌表达。从新生小鼠骨骼中获取成骨细胞,经碱性磷酸酶(ALP)染色鉴定后,与破骨细胞前体细胞系Raw 264.7在96孔板中共同培养。9天后,向这些共培养体系中加入10 μmol/L阿仑膦酸钠(ALN)、10(-5) g/L rhOPG-Fc、10 μmol/L ALN + 10(-5) g/L rhOPG-Fc、5 μmol/L ALN + 5×10(-6) g/L rhOPG-Fc。未添加上述药物培养的成骨细胞作为对照。在后续第3天和第7天进行抗酒石酸酸性磷酸酶(TRAP)染色阳性细胞计数和皮质骨凹坑形成计数。
十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和蛋白质免疫印迹法(Western blot)显示,表达蛋白的分子量约为55 kDa,且能与抗IgG抗体特异性结合。共培养对照组培养9天后发现许多多核TRAP染色阳性细胞,经TRAP染色证实为成熟破骨细胞。在加入rhOPG-Fc、ALN或两者后的第3天和第7天,rhOPG-Fc组、ALN组或两者联合组的TRAP染色阳性细胞计数和皮质骨凹坑形成计数均显著低于对照组,且联合组(10(-5) g/L rhOPG-Fc + 10 μmol/L ALN)与rhOPG-Fc或ALN单药组相比下降最为显著。
rhOPG-Fc可减少破骨细胞数量并抑制其功能。rhOPG-Fc与ALN联合应用对成熟破骨细胞具有显著的抑制作用。