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在添加和不添加1α,25 - 二羟维生素D3的情况下培养的人牙周膜细胞中骨保护素和核因子κB受体活化因子配体的表达

The expression of osteoprotegerin and the receptor activator of nuclear factor kappa B ligand in human periodontal ligament cells cultured with and without 1alpha,25-dihydroxyvitamin D3.

作者信息

Zhang D, Yang Y Q, Li X T, Fu M K

机构信息

Department of Orthodontics, School of Stomatology, Peking University, 100081, Beijing, PR China.

出版信息

Arch Oral Biol. 2004 Jan;49(1):71-6. doi: 10.1016/s0003-9969(03)00201-2.

DOI:10.1016/s0003-9969(03)00201-2
PMID:14693199
Abstract

The receptor activator of nuclear factor kappa B ligand (RANKL) and its decoy receptor, osteoprotegerin (OPG), are important bone metabolism molecules, which directly control osteoclastogenesis. Periodontal ligament (PDL) cells play a vital role in maintaining the homeostasis of periodontal tissues, releasing cytokines to affect bone metabolism. The purpose of this study was to investigate the expression of OPG and RANKL in cultured human periodontal ligament cells (hPDLCs) derived from permanent teeth and the expression change after stimulation by 1alpha,25-dihydroxyvitamin D(3) (1alpha,25(OH)(2)vitD(3)), a kind of bone resorption promoter. HPDLCs were cultured in the presence or absence of 10(-8)M 1alpha,25(OH)(2)vitD(3) in vitro. The expression of mRNA for OPG and RANKL in hPDLCs during 6 days' culture was examined using semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR). The level of secreted OPG protein in the culture medium during 6 days' culture was detected by enzyme-linked immunoabsorbent assay (ELISA). The result showed that OPG and RANKL were expressed by hPDLCs. OPG expression was down-regulated by 10(-8)M 1alpha,25(OH)(2)vitD(3) in a time-dependent manner, while RANKL mRNA was up-regulated. The ratio of OPG/RANKL was decreased. In conclusion, our findings suggest that hPDLCs may regulate the alveolar bone metabolism through the OPG/RANKL system.

摘要

核因子κB受体活化因子配体(RANKL)及其诱饵受体骨保护素(OPG)是重要的骨代谢分子,直接控制破骨细胞生成。牙周膜(PDL)细胞在维持牙周组织的稳态中起关键作用,通过释放细胞因子影响骨代谢。本研究旨在探讨人恒牙来源的培养牙周膜细胞(hPDLCs)中OPG和RANKL的表达以及在一种骨吸收促进剂1α,25 - 二羟基维生素D(3)(1α,25(OH)₂vitD₃)刺激后的表达变化。hPDLCs在体外有无10⁻⁸M 1α,25(OH)₂vitD₃存在的情况下进行培养。采用半定量逆转录 - 聚合酶链反应(RT-PCR)检测hPDLCs在6天培养过程中OPG和RANKL的mRNA表达。通过酶联免疫吸附测定(ELISA)检测6天培养过程中培养基中分泌的OPG蛋白水平。结果显示hPDLCs表达OPG和RANKL。10⁻⁸M 1α,25(OH)₂vitD₃以时间依赖性方式下调OPG表达,而RANKL mRNA上调。OPG/RANKL比值降低。总之,我们的研究结果表明hPDLCs可能通过OPG/RANKL系统调节牙槽骨代谢。

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