Ferreira Lino S, Gerecht Sharon, Fuller Jason, Shieh Hester F, Vunjak-Novakovic Gordana, Langer Robert
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Biomaterials. 2007 Jun;28(17):2706-17. doi: 10.1016/j.biomaterials.2007.01.021. Epub 2007 Jan 16.
We propose a new methodology to enhance the vascular differentiation of human embryonic stem cells (hESCs) by encapsulation in a bioactive hydrogel. hESCs were encapsulated in a dextran-based hydrogel with or without immobilized regulatory factors: a tethered RGD peptide and microencapsulated VEGF(165). The fraction of cells expressing vascular endothelial growth factor (VEGF) receptor KDR/Flk-1, a vascular marker, increased up to 20-fold, as compared to spontaneously differentiated embryoid bodies (EBs). The percentage of encapsulated cells in hydrogels with regulatory factors expressing ectodermal markers including nestin or endodermal markers including alpha-fetoprotein decreased 2- or 3-fold, respectively, as compared to EBs. When the cells were removed from these networks and cultured in media conditions conducive for further vascular differentiation, the number of vascular cells was higher than the number obtained through EBs, using the same media conditions. Functionalized dextran-based hydrogels could thus enable derivation of vascular cells in large quantities, particularly endothelial cells, for potential application in tissue engineering and regenerative medicine.
我们提出了一种新方法,通过将人胚胎干细胞(hESCs)封装在生物活性水凝胶中来增强其血管分化。hESCs被封装在含有或不含有固定化调节因子的基于右旋糖酐的水凝胶中:一种连接的RGD肽和微囊化的VEGF(165)。与自发分化的胚状体(EBs)相比,表达血管标志物血管内皮生长因子(VEGF)受体KDR/Flk-1的细胞比例增加了20倍。与EBs相比,在含有调节因子的水凝胶中封装的细胞中,表达包括巢蛋白在内的外胚层标志物或包括甲胎蛋白在内的内胚层标志物的细胞百分比分别降低了2倍或3倍。当将细胞从这些网络中取出并在有利于进一步血管分化的培养基条件下培养时,在相同培养基条件下,血管细胞的数量高于通过EBs获得的数量。因此,功能化的基于右旋糖酐的水凝胶能够大量衍生血管细胞,特别是内皮细胞,用于组织工程和再生医学的潜在应用。