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Dental Tissue Engineering of EMPs on Human Dental Pulp Stem Cells

机译:人体牙髓干细胞EMPS的牙科组织工程

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The aim of this study was to isolate and characteristics human dental pulp stem cells (hDPSCs) derived from human third molar pulp. Another aim was to verify the expression with dentin sialoprotein (DSPP), dentin sialoprotein (DSP), dentin matrixprotein 1 (DMP-1) and vimentin. For characterisation, proliferation capacity, phenotypic properties, and differentiation characteristics were utilised. Stem cells isolated from hNDP were analysed by flow cytometry and immunocytochemistry. Cell line were directionally differentiated towards adipogenic, osteogenic chondrogenic, myogenic and neurogenic lineages. The expression of DSPP, DSP, DMP-1and vimentin, as analyzed by Immunocytochemistry, increased after EMPs incubating for 5d. So exhibit multilineage differentiation properties. Thus, both EMPs are important during hDPSCs proliferation. During cytodifferentiation, EMPs are essential for the complete differentiation of odontoblasts by up-regulating the expression of DSPP, DSP, DMP-1 and vimentin. Stimulation of these cells by EMPs significantly increases alkaline phosphatase(ALP) activity. ALP activity was expressed as OD 405 nm/mg of protein A increase was observed in ALP activity of hDPSCs during the culturing of EMPs. According to the differentiation and proliferation potential of HDPSC was shown. A specific function for EMPs up-regulat in differentiation of hDPSCs was elucidated.
机译:本研究的目的是分离和特征衍生自人第三磨牙浆的人牙牙髓干细胞(HDPSC)。另一种目的是验证用牙本质唾液酸蛋白(DSPP),牙本质唾液酸蛋白(DSP),牙本质基质蛋白1(DMP-1)和Vimentin的表达。用于使用表征,增殖能力,表型特性和分化特征。通过流式细胞术和免疫细胞化学分析从HNDP中分离的干细胞。细胞系定向朝向脂肪发生,骨质发生的软骨内,肌原素和神经源性谱系分化。如免疫细胞化学分析,DSPP,DSP,DMP-1和Vimentin的表达,EMPS孵育5D的EMPS后增加。所以表现出多线性分化特性。因此,两种EMPS在HDPSCS增殖期间都很重要。在细胞对齐期间,EMPS通过UP调节DSPP,DSP,DMP-1和Vimentin的表达来完全分化Odontoblasts。 EMPS对这些细胞的刺激显着增加了碱性磷酸酶(ALP)活性。 ALP活性被表示为OD 405nm / mg蛋白,在培养EMPS期间在HDPSC的ALP活性中观察到增加。根据HDPSC的分化和增殖电位显示。阐明了HDPSCS分化的EMPS上高稳定的特定功能。

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