Wang Kai, Chen Xuejiao, Pan Yiwa, Cui Yun, Zhou Xin, Kong Deling, Zhao Qiang
State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, Nankai University, Tianjin 300071, China.
Biomed Res Int. 2015;2015:865076. doi: 10.1155/2015/865076. Epub 2015 Mar 25.
Creating a long-lasting and functional vasculature represents one of the most fundamental challenges in tissue engineering. VEGF has been widely accepted as a potent angiogenic factor involved in the early stages of blood vessel formation. In this study, fibrous scaffolds that consist of PCL and gelatin fibers were fabricated. The gelatin fibers were further functionalized by heparin immobilization, which provides binding sites for VEGF and thus enables the sustained release of VEGF. In vitro release test confirms the sustained releasing profile of VEGF, and stable release was observed over a time period of 25 days. In vitro cell assay indicates that VEGF release significantly promoted the proliferation of endothelial cells. More importantly, in vivo subcutaneous implantation reflects that vascularization has been effectively enhanced in the PCL/gelatin scaffolds compared with the PCL counterpart due to the sustained release of VEGF. Therefore, the heparinized PCL/gelatin scaffolds developed in this study may be a promising candidate for regeneration of complex tissues with sufficient vascularization.
构建持久且功能健全的脉管系统是组织工程领域最基本的挑战之一。血管内皮生长因子(VEGF)作为一种强效血管生成因子,在血管形成的早期阶段发挥作用,已被广泛认可。在本研究中,制备了由聚己内酯(PCL)和明胶纤维组成的纤维支架。通过固定肝素对明胶纤维进行进一步功能化处理,肝素可为VEGF提供结合位点,从而实现VEGF的持续释放。体外释放试验证实了VEGF的持续释放特性,在25天的时间段内观察到了稳定释放。体外细胞试验表明,VEGF的释放显著促进了内皮细胞的增殖。更重要的是,体内皮下植入实验表明,由于VEGF的持续释放,与PCL支架相比,PCL/明胶支架中的血管化得到了有效增强。因此,本研究中开发的肝素化PCL/明胶支架有望成为具有充分血管化的复杂组织再生的候选材料。