壳聚糖
血管生成
硫酸化
脐静脉
化学
脚手架
组织工程
生物化学
一氧化氮
体外
细胞生物学
生物医学工程
生物
有机化学
医学
癌症研究
作者
Guijuan Han,Xiaohui Xia,Zhicheng Pan,Yucheng Lin,Lihua Li,Yanpeng Jiao,Changren Zhou,Shan Ding
标识
DOI:10.1080/09205063.2019.1702764
摘要
The vascularization within the scaffold is still a significant challenge in tissue engineering applications. Sulfated chitosan (SCS) as an amazing substance have been used in tissue engineering to stimulate angiogenesis. However, it is not clear whether they have difference in the ability to promote vascularization of SCS with different sulfonic acid group sites. The aim of this study was to evaluate human umbilical vein endothelial cells (HUVECs) viability and differentiation in vitro, affected by three types of sulfated chitosan' i.e. 2-N-6-O-sulfated chitosan (2,6-SCS), 3'6-O-sulfated chitosan (3,6-SCS) and 6-O-sulfated chitosan (6-SCS). The results are showed that all the SCS possesses excellent biological properties to promote HUVECs viability and proliferation. Especially, 2,6-SCS promotes desirable intracellular nitric oxide secretion and capillary tube formation. Meanwhile, 2,6-SCS up-regulate the related gene and protein expression compared with other sulfonic acid group sites SCS and heparin. Therefore, 2,6-SCS is a promising substitute material for angiogenesis and as aqueous formulation can be employed to fabrication functionalization scaffold surface with promoted angiogenesis.
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