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本帖最后由 细胞海洋 于 2012-2-21 16:59 编辑
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摘要:目的:体外培养、鉴定人牙周膜干细胞(periodontal ligament stem cells,PDLSCs)并定向诱导分化为成骨细胞,探讨人PDLSCs的多向分化潜能:方法:体外分离、培养人牙周膜细胞,待细胞达一定量后用有限稀释法进行克隆化培养,筛选鉴定牙周膜干细胞(PDLSC),矿化诱导培养21d后检测钙结节形成情况、ALP活性,免疫细胞化学检测骨涎蛋白(BSP)、Ⅰ型胶原表达,RT—PCR检测ALP、BSP mRNA表达。结果:人PDLSCs体外诱导培养21d后可见钙结节形成,成骨细胞相关蛋白及mRNA均阳性表达。结论:人PDLSCs在体外诱导条件下具有成骨潜能。: T( k' b% m7 F. Y: M
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KeyWord:human periodontal ligament stem cells; cell cloning; induced differentiation& d1 ^2 j p, X5 G( v7 u/ g! @0 O/ I
, p ~& B# W) E6 c关键词:牙周膜干细胞 细胞克隆 诱导分化
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分类号:Q813.12 Q813.5[著者标引]文献标识码:A文章编号:1005-4979(2008)05-0318-05: ~" S9 e! {3 ^ D: J, S \3 p
Human Periodontal Ligament Stem Cells Differentiation into Osteoblasts in vitro ZHEN Lei, LIU Hong-wei Department of Oral Medicine, Hospital of Stomatology, Tongji University, Shanghai 200072, China
* Y" {" h/ Q( n; k4 P1 R6 O& H+ QAbstract:Objective: To isolate and purify the human periodontal ligament stem cells(PDLSCs) and investigate the differentiation potentials of PDLSC into osteoblasts in vitro. Methods: PDLSCs were isolated and cultivated. PDLSCs of passage 2 was plated at density of 5×10^3/cm^2. At 80% confluence, the medium was changed to an inducing medium. After 21 days of induction, the results were evaluated by Alizarin red S staining, ALP activitv test, immunohistochemistry and RT-PCR. Results: PDLSCs were cultivated and differentiated in vitro with active function, which were manifested by Alizarin red S staining and ALP activity test. Positive expression of collagen Ⅰ , BSP, ALP were confirmed by immunohistochemistry and RT-PCR. Conclusion: PDLSCs can be induced into osteoblasts in vitro. PDLSCs have the capability of multilineage differentiations.4 v- U$ C8 P: ?
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KeyWord:human periodontal ligament stem cells; cell cloning; induced differentiation7 q% R- N( b2 @
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