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1,25-(OH)_2D_3作用下人牙周膜细胞破骨细胞分化因子及破骨细胞发生抑制因子的表达及意义 被引量:3

Effects of 1,25-(OH)_2D_3 stimulation on expression of ODF and OCIF by human periodontal ligament cells
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摘要 目的观察1,25-二羟基维生素D3[1,25-(OH)2D3]对体外人牙周膜细胞(HPDLC)破骨细胞分化因子(ODF)mRNA及破骨细胞发生抑制因子(OCIF)mRNA表达的影响,探讨正畸牙周组织改建的分子机制。方法以不同浓度的1,25-(OH)2D3(0、1×10-10、1×10-8、1×10-6mol/L)作用于体外培养的人牙周膜细胞,利用原位杂交染色及RT-PCR检测技术,检测不同浓度的1,25-(OH)2D3作用于体外培养人牙周膜细胞ODF、OCIFmRNA表达的强度变化。结果随1,25-(OH)2D3浓度的升高,人牙周膜细胞ODFmRNA的表达升高,而OCIFmRNA的表达降低。结论1,25-(OH)2D3在体外可影响人牙周膜细胞ODFmRNA和OCIFmRNA的表达,从而通过调节ODF和OCIF相对含量的变化,影响牙周组织改建过程。 Objective To clarify the molecular mechanism of periodontal tissue remodeling during orthodontic tooth movement by investigating the effects of 1,25-(OH)2D3 on the expression of ODF and OCIF in hmnan periodontal ligament cells (HPDLCs). Methods HPDLCs were subjected to different doses of 1,25-(OH)eD3(0, 1 × 10^-10,1 × 10^-8, 1 ×10^-6 mol/L) for 24 hours in this experiment, mRNA expression of ODF and OCIF were detenninod by semi quantitative RT-PCR approach. Results The expression of ODF mRNA and increased significantly in a dose-dependent manner,and the expression of OCIF mRNA didn't decrease not significantly. Conclusion 1,25-( OH)eD3 could adjust the proportion of expression of ODF to expression of OCW. Thus, the hone metabolism was adjusted.
出处 《口腔医学》 CAS 2007年第2期57-60,共4页 Stomatology
基金 国家自然科学基金资助项目(30300393)
关键词 破骨细胞分化因子 破骨细胞发生抑制因子 牙周膜细胞 1 25-二羟基维生素D3 osteoclast differentiation factor osteoclasto-genesis inhibitory factor periodontal ligament cell 1,25-(OH)2D3
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