摘要
目的探讨成牙骨质样细胞OCCM-30在不同时间缺氧微环境下破骨功能的调节变化。方法利用三气培养箱构建细胞缺氧模型,以常氧条件培养为对照组,应用RT-PCR检测缺氧后OCCM-30细胞骨桥蛋白(OPN)、骨保护素(OPG)、核因子κB受体活化因子配体(RANKL)mRNA表达的变化。结果 OPN mRNA的表达随缺氧时间逐步上调,36h达到顶峰后进入平台期。OPG mRNA的表达,随着缺氧的开始快速上调,在12h达到顶峰后进入平台期,在36h后逐步下降;RANKL mRNA的诱导表达呈现先上升后下降的趋势。结论缺氧微环境能显著诱导OCCM-30细胞表达破骨调节功能。
Objective To investigate the influence of hypoxia to the osteoclast function related gene of OCCM-30 cell. Methods Use special incubator to construct hypoxic model, take the cell cultured under normal oxygenic pressure as control and use RT-PCR method to measure the genetic expression of OPN, OPG and RANKL mRNA. Results The expression of OPN mR-NA could be induced by hypoxia and reached the highest point at 36h;the expression of OPG mRNA could be induced quickly by hypoxia and reached the highest platform at 12h, then decreased after 36h;the expression of RANKL mRNA showed a downward trend after the first rise. Conclusion The hypoxia could obviously induced osteoclast function of OCCM-30 cell.
出处
《四川医学》
CAS
2015年第9期1253-1255,共3页
Sichuan Medical Journal
关键词
缺氧
成牙骨质样细胞
破骨功能
hypoxia
cementoblast-like cell
osteoclast function