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Shear stress and VEGF enhance endothelial differentiation of human adipose-derived stem cells

机译:剪应力和VEGF增强人脂肪干细胞的内皮细胞分化

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Herein we combine chemical and mechanical stimulation to investigate the effects of vascular endothelial growth factor (VEGF) and physiological shear stress in promoting the differentiation human adipose derived stem cells (ADSCs) into endothelial cells. ADSCs were isolated and characterized; endothelial differentiation was promoted by culturing confluent cells in 50 ng/ml VEGF under physiological shear stress for up to 14 days. Afterwards, endothelial cells were seeded onto collagen or acellular aortic valve matrices and exposed to four culture conditions: shear stress + VEGF; shear stress - VEGF; static + VEGF and static - VEGF. After 7 days, phenotype was investigated. ADSCs subjected to shear stress and VEGF express a comprehensive range of specific endothelial markers (vWF, eNOS and FLT-1 after 7 days and CD31, FLk-1 and VE-cadherin after 14 days) and maintain the phenotype when seeded onto scaffolds. Our protocol proved to be an efficient source of endothelial-like cells for tissue engineering based on autologous ADSC.
机译:本文中,我们结合化学和机械刺激来研究血管内皮生长因子(VEGF)和生理切应力在促进人类脂肪衍生干细胞(ADSCs)分化为内皮细胞中的作用。分离并鉴定了ADSC;通过在生理切应力下在50 ng / ml VEGF中培养融合细胞长达14天来促进内皮细胞分化。之后,将内皮细胞接种到胶原蛋白或无细胞主动脉瓣膜基质上,并暴露于四种培养条件下:剪切应力+ VEGF;剪应力-VEGF;静态+ VEGF和静态-VEGF。 7天后,研究表型。经受剪切应力和VEGF的ADSC会表达一系列全面的特异性内皮标志物(7天后表达vWF,eNOS和FLT-1,14天后表达CD31,FLk-1和VE-钙粘蛋白)并在植入支架上时保持表型。我们的协议被证明是基于自体ADSC的组织工程内皮样细胞的有效来源。

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