Khanmohammadi Mehdi, Sakai Shinji, Taya Masahito
Division of Chemical Engineering, Department of Materials Science and Engineering, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama-cho, Toyonaka, Osaka 560-8531, Japan.
Division of Chemical Engineering, Department of Materials Science and Engineering, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama-cho, Toyonaka, Osaka 560-8531, Japan.
Int J Biol Macromol. 2017 Apr;97:308-316. doi: 10.1016/j.ijbiomac.2016.12.088. Epub 2017 Jan 12.
The hydrogels having the ability to promote migration and morphogenesis of endothelial cells (ECs) are useful for fabricating vascularized dense tissues in vitro. The present study explores the immobilization of low molecular weight hyaluronic acid (LMWHA) derivative within gelatin-based hydrogel to stimulate migration of ECs. The LMWHA derivative possessing phenolic hydroxyl moieties (LMWHA-Ph) was bound to gelatin-based derivative hydrogel through the horseradish peroxidase-catalyzed reaction. The motility of ECs was analyzed by scratch migration assay and microparticle-based cell migration assay. The incorporated LMWHA-Ph molecules within hydrogel was found to be preserved stably through covalent bonds during incubation. The free and immobilized LMWHA-Ph did not lose an inherent stimulatory effect on human umbilical vein endothelial cells (HUVECs). The immobilized LMWHA-Ph within gelatin-based hydrogel induced the high motility of HUVECs, accompanied by robust cytoskeleton extension, and cell subpopulation expressing CD44 cell receptor. In the presence of immobilized LMWHA-Ph, the migration distance and the number of existing HUVECs were demonstrated to be encouraged in dose-dependent and time-dependent manners. Based on the results obtained in this work, it was concluded that the enzymatic immobilization of LMWHA-Ph within gelatin-based hydrogel represents a promising approach to promote ECs' motility and further exploitation for vascular tissue engineering applications.
具有促进内皮细胞(ECs)迁移和形态发生能力的水凝胶可用于体外构建血管化致密组织。本研究探索了将低分子量透明质酸(LMWHA)衍生物固定在明胶基水凝胶中以刺激ECs迁移。具有酚羟基部分的LMWHA衍生物(LMWHA-Ph)通过辣根过氧化物酶催化反应与明胶基衍生物水凝胶结合。通过划痕迁移试验和基于微粒的细胞迁移试验分析ECs的运动性。发现在孵育过程中,水凝胶中掺入的LMWHA-Ph分子通过共价键稳定保存。游离和固定化的LMWHA-Ph对人脐静脉内皮细胞(HUVECs)均未失去其固有的刺激作用。明胶基水凝胶中固定化的LMWHA-Ph诱导HUVECs具有高运动性,同时伴有强大的细胞骨架延伸以及表达CD44细胞受体的细胞亚群。在存在固定化LMWHA-Ph的情况下,HUVECs的迁移距离和现存数量呈剂量依赖性和时间依赖性增加。基于本研究获得的结果,得出结论:LMWHA-Ph在明胶基水凝胶中的酶促固定是促进ECs运动性的一种有前景的方法,可进一步用于血管组织工程应用。