The next generation of endothelial differentiation: Tissue-specific ECs

被引:41
|
作者
Nguyen, Jane [1 ]
Lin, Ying-Yu [1 ]
Gerecht, Sharon [1 ,2 ,3 ,4 ]
机构
[1] Johns Hopkins Univ, Phys Sci Oncol Ctr, Inst NanoBioTechnol, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Mat Sci & Engn, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
关键词
PLURIPOTENT STEM-CELLS; IN-VITRO; EPICARDIAL PROGENITORS; CARDIAC MICROTISSUES; BARRIER; MODEL; GROWTH; LIVER; ORGANOIDS; MIGRATION;
D O I
10.1016/j.stem.2021.05.002
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Endothelial cells (ECs) sense and respond to fluid flow and regulate immune cell trafficking in all organs. Despite sharing the same mesodermal origin, ECs exhibit heterogeneous tissue-specific characteristics. Human pluripotent stem cells (hPSCs) can potentially be harnessed to capture this heterogeneity and further elucidate endothelium behavior to satisfy the need for increased accuracy and breadth of disease models and therapeutics. Here, we review current strategies for hPSC differentiation to blood vascular ECs and their maturation into continuous, fenestrated, and sinusoidal tissues. We then discuss the contribution of hPSC-derived ECs to recent advances in organoid development and organ-on-chip approaches.
引用
收藏
页码:1188 / 1204
页数:17
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