内皮细胞微血管形成纤维蛋白凝胶微槽模型的建立

Q4 Engineering Journal of Biorheology Pub Date : 2015-01-01 DOI:10.17106/JBR.29.19
Shaoyi Chen, A. Morita, I. Sukmana, Eijiro Maeda, T. Ohashi
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引用次数: 1

摘要

本研究旨在开发一种具有纤维蛋白凝胶-微槽结构的新型实验装置,用于内皮细胞(ECs)微血管化的研究。研究了微槽宽度、初始细胞播种密度和添加血管内皮生长因子(VEGF)对内皮细胞体外微血管形成的影响。ECs在聚二甲基硅氧烷微槽底物上形成的纤维蛋白凝胶中培养,微槽宽度分别为50、100、150和200 μm。在所有四种类型的微槽中,ECs都在凝胶中伸长并发芽。此外,在100μm微沟槽中,经常观察到细胞分支连接形成的多细胞网络。高初始细胞密度和VEGF对细胞形态变化均有显著的促进作用。研究结果表明,微槽结构对内皮细胞具有几何约束作用,对内皮细胞的血管生成反应具有促进作用,因此可以作为体外血管形成研究的实验模型。
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Development of fibrin gel-microgroove model for microvascularization by endothelial cells
This study was performed to develop a new experimental device with a fibrin gel-microgroove structure for study of microvascularization by endothelial cells (ECs). The effects of the width of microgrooves, initial cell seeding density and a supplementation of vascular endothelial growth factor (VEGF) on in vitro microvasculaization of ECs were examined. ECs were cultured in a fibrin gel formed on a polydimethylsiloxane microgroove substrate, with the microgroove width of 50, 100, 150 and 200 μm. ECs were elongated and sprouted within the gel in all the four types of microgrooves. In addition, multicellular network by connected cell branches were frequently observed in 100μm microgrooves. Both high initial cell density and VEGF demonstrated significant promotional effects on morphology changes. The findings indicate that microgroove structure serves as a geometrical constraint for ECs, with a promotional effect on angiogenic responses of ECs, and thus, it can be used as an experimental model in the study of in vitro vascularization.
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来源期刊
Journal of Biorheology
Journal of Biorheology Engineering-Mechanical Engineering
CiteScore
0.50
自引率
0.00%
发文量
5
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