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论文摘要

骨髓间充质干细胞骨向诱导分化过程中破骨细胞分化因子和细胞间粘附分子-1的表达变化

Expression of Osteoclast Differentiation Factor and Intercellular Adhesion Molecule-1 of Bone Marrow Mesenchymal Stem Cells Enhanced with Osteogenic Differentiation

作者:王军,赵志河,罗颂椒,樊瑜波

Author:WANG Jun1,ZHAO Zhi-He1,LUO Song-jiao1,FAN Yu-bo2

收稿日期:2005-06-25          年卷(期)页码:2005,23(03):240-

期刊名称:华西口腔医学杂志

Journal Name:West China Journal of Stomatology

关键字:骨髓间充质干细胞,成骨细胞,破骨细胞分化因子,细胞间粘附分子-1,

Key words:rat bone marrowmesenchymal stem cells,osteoblasts,osteoclast differentiation factor,intercellular adhesion molecule-1,

基金项目:国家自然科学基金资助项目(10372066,10402027)

中文摘要

目的 观察破骨细胞分化因子(ODF)和细胞间粘附分子-1(ICAM-1)在不同分化状态成骨细胞的表达变 化,探讨正畸牙移动过程中成骨细胞对破骨细胞分化成熟的诱导机制。方法 分离培养大鼠骨髓间充质干细胞, 成骨定向诱导后获得不同分化状态的成骨细胞,RT-PCR检测不同分化状态下的成骨细胞ODF和ICAM-1的表达变 化。结果 成骨细胞在分化成熟过程中,ICAM-1 mRNA表达水平逐渐升高;ODF mRNA则在诱导后6 d开始表达, 并维持在一较稳定的水平。结论 不同分化状态的成骨细胞对破骨细胞诱导分化的能力有所差异,相对成熟的成 骨细胞的诱导能力可能更强。

英文摘要

Objective To investgate whether the expression of osteoclast differentiation factor(ODF), intercellular adhesion molecule-1(ICAM-1) depended on the stage of osteoblastic differentiation from rat bone marrow mesenchymal stem cells(BM- SC).Methods BMSC (4 passage) were selected for osteogenic differentiation by treated with osteogenic supplements(OS). Cells were harvested by day 0, 3, 6, 9, 12, 18 respectively after osteogenic inducement. In each experiment, control and OS- treated cells were processed in parallel. ODF and ICAM-1 mRNAwere analyzed by semiquantitave RT-PCR assay.Results Expression of ODFwas enhanced with osteogenic differentiation guadully. whereas, expression of ICAM-1 was activated at OS- treated day 6, then keeping at a stable level.Conclusion This study indicated that BMSC undergoing osteogenic inducement was an ideal model for studying the differentiation and maturation of osteoblasts. During the early stage of differentiation along os- teoblasts from stem cells to osteocytes, BMSC or osteoprogenitor react somewhat differently from osteoblasts, suggesting the ability of osteoblasts to regulating differentiation and maturation of osteoclasts have been improved with osteogenic culture.

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