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作 者:李彦[1] 李石 牛忠英[1] 包博[1] 石馨[1]
机构地区:[1]解放军第306医院全军口腔疾病诊治中心 [2]66055部队医院口腔科
出 处:《上海口腔医学》2012年第3期246-250,共5页Shanghai Journal of Stomatology
基 金:国家自然科学基金(30870598)~~
摘 要:目的:了解Smads信号通路在模拟微重力条件下对人牙周膜细胞成骨向分化的影响。方法:自手术拔除的人牙周膜中培养获得牙周膜细胞,利用有限稀释法培养获得人牙周膜细胞(human periodontal ligament cells,hPDLCs)。采用旋转细胞培养系统(rotary cell culture system,RCCS)建立模拟微重力环境,将细胞分为对照组(正常重力组)、模拟微重力组,应用实时定量PCR检测Smads信号分子表达及加入Smads抑制剂后成骨标志物的表达,流式细胞仪检测磷酸化Smad表达。采用SPSS13.0软件包对数据进行统计学处理。结果:与对照组相比,模拟微重力组Smads 2、3、4 mRNA表达量显著增加,呈时间依赖性,在2h达到峰值,随后开始下降。Smads7在2h时开始上升,观测时间内未捕捉到其下降。流式细胞检测发现,p-Smads在30min时开始出现高表达(29.39%),2h时达到峰值,表达量为91.32%。加入Smads抑制剂后,p-Smads表达下降至5.3%,成骨标志物COL1、ALP、OCN表达显著下降(P<0.05)。结论:模拟微重力环境下,Smads信号通路参与了hPDLSCs成骨向分化。PUPOSE: To investigate the effect of Smads signal pathway on the osteogenesis of human periodontal ligament stem cells (hPDLSCs) in simulated mierogravity. METHODS: Human periodontal ligament stem cells were isolated from the ligament of surgically extracted human teeth.Through limiting dilution assay, mono-clone of the cell was obtained, hPDLSCs were isolated from MesenPRO RS medium. Rotary eel] culture system (RCCS) was enrolled to set simulated microgravity (SMG). Samples were set to control group (normal gravity group, NG) and simulated mierogravity group (SMG). Real-time PCR was used to detect the expression of Smads signals and the expression of markers of osteogenesis before and after SIS3. The amount of phosphated-Smad was assayed by flow eytometry. Statistical analysis of the data was clone by ANOVA with SPSS 13.0 software package. RESULTS: Compared with that of the control group, the expression of Smads 2,3,4 was significantly higher in SMG group (P〈0.05)in a time-dependent manner. Flow eytometry assay showed increased expression of p-Smads at 30-min, and peak expression was observed at 2h,reaehing at 91.32%. The addition of SIS3 led to significant decrease of COL I, ALP, OCN and p-Smads (P〈0.05). CONCLUSION: Smads signal pathway was enrolled in the osteogenesis of hPDLSCs in simulated microgravity.
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