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Fibrinogen Concentration Influence on VEGF-Induced Differentiation of Adipose Tissue-Derived Stem Cells into Endothelial Cells

机译:纤维蛋白原浓度对VEGF诱导的脂肪组织衍生干细胞分化为内皮细胞的影响

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Fibrin is a natural substrate for growth, adhesion, and migration of mature endothelial cells (ECs) and a candidate coating material in approaches to graft endothelialization. Adipose tissue represents an abundant, practical source of donor tissue for stem cells which may be a useful source for engineering of vascular grafts. However, the optimal substrates that promote differentiation of adipose tissue-derived stem cells (ASCs) into ECs remain to be elucidated. In the present study, we investigated whether fibrin can be used as a substratum to support in vitro ECs differentiation of ASCs and whether fibrinogen concentration can be affect on ECs differentiation of ASCs. For determination of phenotypic characteristics of ASCs used in this experiment, we performed flow cytometry analysis. ASCs were plated on fibrin composed of varying concentrations of fibrinogen and induced into ECs differentiation in presence of VEGF. Before inducing into ECs, ASCs did not express any markers of hematopoietic cells (CD34, CD45), ECs (CD31, CD34), and endothelial progenitor cells (CD34, CD133, Flk-1). The degree of ECs differentiation was determined by capillary network formation, ECs-specific gene expression, and F-actin assembly. During the first 12 h after seeding, cells spread randomly, moved and formed small interconnected clusters. These clusters decreased in size and formed a capillary tube at 48 h. During the further incubation in presence of VEGF for 7 days, ASCs expressed mRNA and protein of von Willebrand factor (vWF). The degree of ECs differentiation of ASCs was consistently decreased as fibrinogen concentration increase. Fibrin may be used as biomatrix to promote differentiation of ASCs into ECs for tissue engineering.
机译:纤维蛋白是用于成熟内皮​​细胞(ECS)的生长,粘附和迁移的天然基质,以及移植内皮化方法的候选涂层材料。脂肪组织代表干细胞的丰富,实用的供体组织来源,其可以是血管移植物的工程来源的有用来源。然而,促进脂肪组织衍生的干细胞(ASCS)分化为ECS的最佳底物仍然被阐明。在本研究中,我们研究了纤维蛋白是否可以用作抑制ASC的体外ECS分化的纤维蛋白,以及纤维蛋白原浓度是否可以影响ASC的EC分化。为了测定本实验中使用的ASC的表型特性,我们进行了流式细胞术分析。在纤维蛋白上涂覆由不同浓度的纤维蛋白原组成的纤维蛋白,并在VEGF存在下诱导ECS分化。在诱导ECS之前,ASCS未表达造血细胞(CD34,CD45),ECS(CD31,CD34)和内皮祖细胞(CD34,CD133,FLK-1)的任何标记。 ECS分化程度由毛细管网络形成,ECS特异性基因表达和F-actin组件测定。在播种后的前12小时期间,细胞随机地扩散,移动和形成的小互连簇。这些簇的尺寸减小并在48小时内形成毛细管。在VEGF存在的进一步孵育7天期间,ASCS表达von Willebrand因子(VWF)的mRNA和蛋白质。随着纤维蛋白原浓度的增加,ASCS的ECS分化程度始终降低。纤维蛋白可以用作生物斑纹,以促进ASC的分化为组织工程的ECS。

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