Transient ETV2 Expression Promotes the Generation of Mature Endothelial Cells from Human Pluripotent Stem Cells

被引:8
|
作者
Zhang, Hongyan [1 ,2 ]
Yamaguchi, Tomoko [2 ]
Kokubu, Yasuhiro [2 ]
Kawabata, Kenji [1 ,2 ]
机构
[1] Osaka Univ, Grad Sch Pharmaceut Sci, Lab Biomed Innovat, 1-6 Yamadaoka, Suita, Osaka 5650871, Japan
[2] Natl Inst Biomed Innovat Hlth & Nutr, Lab Stem Cell Regulat, 7-6-8 Saito Asagi, Ibaraki, Osaka 5670085, Japan
关键词
endothelial cell; induced pluripotent stem cell; ETV2; doxycycline-inducible system; HUMAN FIBROBLASTS; EFFICIENT DIFFERENTIATION; ACTS DOWNSTREAM; BLOOD; CONVERSION;
D O I
10.1248/bpb.b21-00929
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Differentiation protocols are used for induced pluripotent stem cells (iPSCs) in in vitro disease modeling and clinical applications. Transplantation of endothelial cells (ECs) is an important treatment strategy for ischemic diseases. For example, in vitro generated ECs can be used to provide the vascular plexus to regenerate organs such as the liver. Here, we demonstrate that the E-twenty-six (ETS) transcription factor ETV2 alone can directly convert iPSCs into vascular endothelial cells (iPS-ETV2-ECs) with an efficiency of over 90% within 5 d. Although the stable overexpression of ETV2 induced the expression of multiple key factors for endothelial development, the induced ECs were less mature. Furthermore, doxycycline-inducible transient ETV2 expression could upregulate the expression of von Willebrand factor (vWF) in iPS-ETV2-ECs, leading to a mature phenotype. The findings of this study on generation of mature iPS-ETV2-ECs provide further insights into the exploration of cell reprogramming from iPSCs. Here, we provide a new protocol for differentiation of iPSCs, thus providing a new source of ECs for in vitro disease modeling and clinical applications.
引用
收藏
页码:483 / 490
页数:8
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