周细胞
诱导多能干细胞
细胞生物学
胚状体
组织工程
角质形成细胞
人诱导多能干细胞
人口
干细胞
生物
内皮干细胞
化学
细胞培养
医学
胚胎干细胞
体外
生物化学
遗传学
环境卫生
基因
作者
Selin Pars,Kevin Achberger,Alexander Kleger,Stefan Liebau,Natalia Pashkovskaia
出处
期刊:Cells
[MDPI AG]
日期:2021-01-05
卷期号:10 (1): 74-74
被引量:9
标识
DOI:10.3390/cells10010074
摘要
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.
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