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作 者:潘建锋[1] 郭常安[1] 沈剑锋[2] 刘嘉[1] 阎作勤[1]
机构地区:[1]复旦大学附属中山医院骨科,上海200032 [2]复旦大学材料科学系
出 处:《中华实验外科杂志》2013年第5期1013-1015,共3页Chinese Journal of Experimental Surgery
基 金:基金项目:国家自然科学基金资助项目(81071468、81171671)
摘 要:目的观察血清、转化生长因子(TGF)-β3、血小板衍生生长闪子(PDGF)-AB、骨形态发生蛋白(BMP)-2、成纤维细胞生长因子(FGF)对兔滑膜间充质干细胞(SMSCs)迁移的影响。方法选取含浓度0.1%、0.5%、1.0%、2.0%、5.0%、10.0%、20.0%血清以及含50μg/LTGF-β3、PDGF—AB、BMP-2、FGF的低糖DMEM作用于兔SMSCs,Transwell小室检测其迁移能力。结果 血清、TGF-β3、PDGF—AB、BMP-2、FGF均可趋化兔SMSCs迁移,血清浓度为5.0%时趋化作用较其他浓度组明显,每×100倍视野下迁移细胞数为(169.00±21.74)个,4种因子中PDGF—AB趋化作用较TGF—β3、BMP-2、FGF明显(219.83±11.29比84.50±10.33、146.67±17.91、99.37±12.27)。结论兔SMSCs可在TGF-β3、PDGF—AB、BMP-2、FGF作用下迁移,其中PDGF—AB趋化最明显,可用于促进SMSCs迁移归巢,进行软骨原位冉生的修复研究。Objective To explore the chemotactic migration effects of serum, transforming growth factor (TGF)-β3, platelet derived growth factor (PDGF)-AB, bone morphogenetic protein (BMP)-2, and fibroblast growth factor (FGF) on rabbit synovium-derived mesenchymal stem cells (SMSCs). Methods The SMSCs were obtained with passage isolation, and then stimulated by low-glucose DEME containing TGF-β3, PDGF-AB, BMP-2, FGF with 50 p^g/L concentration as well as 0. 1% , 0. 5% , 1.0% , 2.0% , 5.0%, 10. 0%, 20. 0% serum. The migration of SMSCs under five different ehemotaetic factors was observed in Transwell chamber assays. Results TGFq33, PDGF-AB, BMP-2, FGF and serum consistently enhanced the migration activity of rabbit SMSCs. Compared with other concentration, 5.0% is the appropriate concentration for serum to induce the migration of rabbit SMSCs. The average numbers of migratory cells (SMSCs) at × 100 magnification was 169. 00 ±21.74 in lower chamber under the 5.0% serum within the Transwell assay. Among the four growth factors, PDGF-AB showed more potent chemotactic effect than otherthree (219.83 ±11.29 vs. 84.50±10.33, 146.67±17.91, 99.37 ±12.27). Conclusion The migration of SMSCs from rabbit could be enhanced by TGF-β, PDGF-AB, BMP-2 and FGF. PDGF-AB is the most potent chemotactic factor among the four growth factors, and may he useful to promote cell homing and cartilage regeneration in situ during cartilage repair.
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