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首页> 外文期刊>International journal of molecular medicine >Shear stress promotes differentiation of stem cells from human exfoliated deciduous teeth into endothelial cells via the downstream pathway of VEGF-Notch signaling
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Shear stress promotes differentiation of stem cells from human exfoliated deciduous teeth into endothelial cells via the downstream pathway of VEGF-Notch signaling

机译:剪切应力通过VEGF-Notch信号传导的下游途径促进将干细胞与人脱色落叶齿的分化成内皮细胞

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Effects of shear stress on endotheliaxl differentiation of stem cells from human exfoliated deciduous teeth (SHEDs) were investigated. SHEDs were treated with shear stress, then reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was performed to analyse the mRNA expression of arterial markers and western blot analysis was performed to analyse protein expression of angiogenic markers. Additionally, in vitro matrigel angiogenesis assay was performed to evaluate vascular-like structure formation. The secreted protein expression levels of the vascular endothelial growth factor (VEGF) of SHEDs after shear stress was also quantified using corresponding ELISA kits. Untreated SHEDs seeded on Matrigel cannot form vessel-like structures at any time points, whereas groups treated with shear stress formed a few vessel-like structures at 4, 8 and 12 h. When SHEDs were treated with EphrinB2-siRNA for 24, the capability of vessel-like structure formation was suppressed. After being treated with shear stress, the expression of VEGF, VEGFR2, DLL4, Notchl, EphrinB2, Hey1and Hey2 (arterial markers) gene expression was significantly upregulated, moreover, the protein levels of VEGFR2, EphrinB2, CD31, Notchl, DLL4, Hey1, and Hey2 were also significantly upregulated. Both the mRNA and protein expression levels of EphB4 (venous marker) were downregulated. The average VEGF protein concentration in supernatants secreted by shear stress treated SHEDS groups increased significantly. In conclusion, shear stress was able to induce arterial endothelial differentiation of stem cells from human exfoliated deciduous teeth, and VEGF-DLL4/Notch-EphrinB2 signaling was involved in this process.
机译:研究了剪切应力对人剥落落叶齿(棚)干细胞的内皮细胞分化的影响。脱落的剪切应力处理,然后进行逆转录定量聚合酶链反应(RT-QPCR)以分析动脉标志物的mRNA表达,并进行Western印迹分析以分析血管生成标记的蛋白质表达。另外,进行体外Matrigel血管生成测定以评估血管状结构形成。使用相应的ELISA试剂盒量化剪切应力后的血管内皮生长因子(VEGF)的分泌蛋白表达水平。在Matrigel上播种的未处理的棚不能在任何时间点形成血管样结构,而用剪切应力处理的基团形成在4,8和12h处的几个容器状结构。当用EphrinB2-siRNA处理SHEDS 24时,抑制了血管状结构的能力。在用剪切应力处理后,VEGF,VEGFR2,DLL4,Notch1,EphrinB2,Hey1和Hey2(动脉标记物)基因表达的表达显着上调,此外,VEGFR2,EphrinB2,CD31,Notchl,DLL4,Hey1,Notch1,DLL4,Hey1,和Hey2也显着上调。 ephb4(静脉标记物)的mRNA和蛋白表达水平都被下调。通过剪切应力处理的脱落组分泌的上清液中的平均VEGF蛋白浓度显着增加。总之,剪切应力能够诱导来自人脱色落叶的干细胞的动脉内皮分化,并且在该过程中涉及VEGF-DLL4 / Notch-EphrinB2信号传导。

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