Generation of Functional Vascular Endothelial Cells and Pericytes from Keratinocyte Derived Human Induced Pluripotent Stem Cells

被引:9
|
作者
Pars, Selin [1 ]
Achberger, Kevin [1 ]
Kleger, Alexander [2 ]
Liebau, Stefan [1 ]
Pashkovskaia, Natalia [1 ]
机构
[1] Eberhard Karls Univ Tubingen, Inst Neuroanat & Dev Biol INDB, Osterbergstr 3, D-72074 Tubingen, Germany
[2] Ulm Univ Hosp, Dept Internal Med 1, D-89081 Ulm, Germany
关键词
human pluripotent stem cells; hiPSC-derived endothelial cells; hiPSC-derived pericytes; vasculature-on-a-chip; self-assembled microvascular network;
D O I
10.3390/cells10010074
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
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.
引用
收藏
页码:1 / 13
页数:13
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