Lin Yang, Gil Chang-Hyun, Yoder Mervin C
From the Department of Pediatrics, Herman B. Wells Center for Pediatric Research (Y.L., C.-H.G., M.C.Y.) and Department of Biochemistry and Molecular Biology (Y.L., M.C.Y.), Indiana University School of Medicine, Indianapolis.
Arterioscler Thromb Vasc Biol. 2017 Nov;37(11):2014-2025. doi: 10.1161/ATVBAHA.117.309962. Epub 2017 Oct 12.
The emergence of induced pluripotent stem cell (iPSC) technology paves the way to generate large numbers of patient-specific endothelial cells (ECs) that can be potentially delivered for regenerative medicine in patients with cardiovascular disease. In the last decade, numerous protocols that differentiate EC from iPSC have been developed by many groups. In this review, we will discuss several common strategies that have been optimized for human iPSC-EC differentiation and subsequent studies that have evaluated the potential of human iPSC-EC as a cell therapy or as a tool in disease modeling. In addition, we will emphasize the importance of using in vivo vessel-forming ability and in vitro clonogenic colony-forming potential as a gold standard with which to evaluate the quality of human iPSC-EC derived from various protocols.
诱导多能干细胞(iPSC)技术的出现为生成大量患者特异性内皮细胞(EC)铺平了道路,这些细胞有可能用于心血管疾病患者的再生医学治疗。在过去十年中,许多研究团队已经开发出了多种从iPSC分化出EC的方案。在这篇综述中,我们将讨论几种经过优化用于人iPSC-EC分化的常见策略,以及随后评估人iPSC-EC作为细胞疗法或疾病建模工具潜力的研究。此外,我们将强调使用体内血管形成能力和体外克隆集落形成潜力作为评估源自各种方案的人iPSC-EC质量的金标准的重要性。