Pars Selin, Achberger Kevin, Kleger Alexander, Liebau Stefan, Pashkovskaia Natalia
Institute of Neuroanatomy & Developmental Biology (INDB), Eberhard Karls University Tübingen, Österbergstrasse 3, 72074 Tübingen, Germany.
Department of Internal Medicine 1, Ulm University Hospital, 89081 Ulm, Germany.
Cells. 2021 Jan 5;10(1):74. doi: 10.3390/cells10010074.
Human induced pluripotent stem cell (hiPSC)-derived endothelial cells (ECs) and pericytes provide a powerful tool for cardiovascular disease modelling, personalized drug testing, translational medicine, and tissue engineering. Here, we report a novel differentiation protocol that results in the fast and efficient production of ECs and pericytes from keratinocyte-derived hiPSCs. We found that the implementation of a 3D embryoid body (EB) stage significantly improves the differentiation efficiency. Compared with the monolayer-based technique, our protocol yields a distinct EC population with higher levels of EC marker expression such as CD31 and vascular endothelial cadherin (VE-cadherin). Furthermore, the EB-based protocol allows the generation of functional EC and pericyte populations that can promote blood vessel-like structure formation upon co-culturing. Moreover, we demonstrate that the EB-based ECs and pericytes can be successfully used in a microfluidic chip model, forming a stable 3D microvascular network. Overall, the described protocol can be used to efficiently differentiate both ECs and pericytes with distinct and high marker expression from keratinocyte-derived hiPSCs, providing a potent source material for future cardiovascular disease studies.
人诱导多能干细胞(hiPSC)来源的内皮细胞(ECs)和平滑肌细胞为心血管疾病建模、个性化药物测试、转化医学和组织工程提供了一个强大的工具。在此,我们报告了一种新的分化方案,该方案可从角质形成细胞来源的hiPSC快速高效地生成ECs和平滑肌细胞。我们发现实施三维胚状体(EB)阶段可显著提高分化效率。与基于单层的技术相比,我们的方案产生了一个独特的EC群体,其EC标志物如CD31和血管内皮钙黏蛋白(VE-钙黏蛋白)的表达水平更高。此外,基于EB的方案允许生成功能性的EC和平滑肌细胞群体,在共培养时可促进血管样结构的形成。此外,我们证明基于EB的ECs和平滑肌细胞可成功用于微流控芯片模型,形成稳定的三维微血管网络。总体而言,所描述的方案可用于从角质形成细胞来源的hiPSC高效分化出具有独特且高标志物表达的ECs和平滑肌细胞,为未来心血管疾病研究提供了一种有力的源材料。