Singh Raminder, Sarker Bapi, Silva Raquel, Detsch Rainer, Dietel Barbara, Alexiou Christoph, Boccaccini Aldo R, Cicha Iwona
Section of Experimental Oncology and Nanomedicine (SEON), Else Kröner-Fresenius-Foundation-endowed Professorship for Nanomedicine, ENT Department, University Hospital Erlangen, Germany.
Department of Cardiology and Angiology, University Hospital Erlangen, Erlangen, Germany.
J Biomed Mater Res A. 2016 Mar;104(3):577-585. doi: 10.1002/jbm.a.35590. Epub 2015 Oct 29.
Developing matrices biocompatible with vascular cells is one of the most challenging tasks in tissue engineering. Here, we compared the growth of vascular cells on different hydrogels as potential materials for bioplotting of vascular tissue. Formulations containing alginate solution (Alg, 2%, w/v) blended with protein solutions (silk fibroin, gelatin, keratin, or elastin) at 1% w/v were prepared. Human umbilical vein endothelial cells (ECs), smooth muscle cells (SMCs), and fibroblasts were cultivated on hydrogels for 7 days. Cell number and morphology was visualised using fluorescent staining at day 3 and 7. Cell metabolic activity was analysed using WST assay. Compared to pure Alg, Alg/keratin, Alg/gelatin and Alg/silk fibroin provided superb surfaces for ECs, supporting their attachment, growth, spreading and metabolic activity. SMCs showed best colonization and growth on Alg/silk fibroin and Alg/keratin hydrogels, whereas on elastin-containing hydrogels, cell clustering was observed. Fibroblasts growth was enhanced on Alg/elastin, and strongly improved on silk fibroin- and keratin-containing hydrogels. In contrast to the previous studies with alginate dialdehyde-gelatin crosslinked gels, Alg/gelatin blend hydrogels provided a less favourable scaffold for fibroblasts. Taken together, the most promising results were obtained with silk fibroin- and keratin-containing hydrogels, which supported the growth of all types of vascular cells. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 577-585, 2016.
开发与血管细胞生物相容的基质是组织工程中最具挑战性的任务之一。在此,我们比较了血管细胞在不同水凝胶上的生长情况,这些水凝胶是用于血管组织生物打印的潜在材料。制备了含有2%(w/v)藻酸盐溶液(Alg)与1%(w/v)蛋白质溶液(丝素蛋白、明胶、角蛋白或弹性蛋白)混合的配方。人脐静脉内皮细胞(ECs)、平滑肌细胞(SMCs)和成纤维细胞在水凝胶上培养7天。在第3天和第7天使用荧光染色观察细胞数量和形态。使用WST测定法分析细胞代谢活性。与纯Alg相比,Alg/角蛋白、Alg/明胶和Alg/丝素蛋白为ECs提供了极好的表面,支持它们的附着、生长、铺展和代谢活性。SMCs在Alg/丝素蛋白和Alg/角蛋白水凝胶上显示出最佳的定植和生长,而在含弹性蛋白的水凝胶上观察到细胞聚集。成纤维细胞在Alg/弹性蛋白上的生长增强,在含丝素蛋白和角蛋白的水凝胶上生长得到显著改善。与先前关于藻酸盐二醛 - 明胶交联凝胶的研究不同,Alg/明胶混合水凝胶为成纤维细胞提供了不太有利的支架。综上所述,含丝素蛋白和角蛋白的水凝胶获得了最有前景的结果,它们支持所有类型血管细胞的生长。© 2015威利期刊公司。《生物医学材料研究杂志》A部分:104A:577 - 585,2016年。