Bao Xiaoping, Lian Xiaojun, Palecek Sean P
Department of Chemical & Biological Engineering, University of Wisconsin, 3637 Engineering Hall, 1415 Engineering Drive, Madison, WI, 53706, USA.
Departments of Biomedical Engineering, Biology, and Huck Institutes of the Life Science, The Pennsylvania State University, University Park, PA, 16802, USA.
Methods Mol Biol. 2016;1481:183-96. doi: 10.1007/978-1-4939-6393-5_17.
Efficient derivation of endothelial cells and their progenitors from human pluripotent stem cells (hPSCs) can facilitate studies of human vascular development, disease modeling, drug discovery, and cell-based therapy. Here we provide a detailed protocol for directing hPSCs to functional endothelial cells and their progenitors in a completely defined, growth factor- and serum-free system by temporal modulation of Wnt/β-catenin signaling via small molecules. We demonstrate a 10-day, two-stage process that recapitulates endothelial cell development, in which hPSCs first differentiate to endothelial progenitors that then generate functional endothelial cells and smooth muscle cells. Methods to characterize endothelial cell identity and function are also described.
从人多能干细胞(hPSC)高效衍生内皮细胞及其祖细胞有助于人类血管发育研究、疾病建模、药物发现和基于细胞的治疗。在此,我们提供了一个详细方案,通过小分子对Wnt/β-连环蛋白信号进行时间调控,在完全确定的、无生长因子和无血清的体系中,将hPSC定向诱导为功能性内皮细胞及其祖细胞。我们展示了一个重现内皮细胞发育的10天两阶段过程,其中hPSC首先分化为内皮祖细胞,然后产生功能性内皮细胞和平滑肌细胞。文中还描述了鉴定内皮细胞特性和功能的方法。