Generation of heart-forming organoids from human pluripotent stem cells

被引:31
作者
Drakhlis, Lika [1 ]
Devadas, Santoshi Biswanath [1 ]
Zweigerdt, Robert [1 ]
机构
[1] Res Ctr Translat Regenerat Med, Leibniz Res Labs Biotechnol & Artificial Organs, Dept Cardiothorac Transplantat & Vasc Surg, Hannover Med Sch, Hannover, Germany
基金
欧盟地平线“2020”;
关键词
IPS CELLS; IN-VITRO; DIFFERENTIATION; MODEL; PROGENITORS; EXPANSION; REVEALS;
D O I
10.1038/s41596-021-00629-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Human pluripotent stem cell aggregates are formed, embedded in Matrigel and directed to differentiate to heart-forming organoids by the chemical WNT pathway modulators CHIR99021 and IWP2. Heart-forming organoids (HFOs) derived from human pluripotent stem cells (hPSCs) are a complex, highly structured in vitro model of early heart, foregut and vasculature development. The model represents a potent tool for various applications, including teratogenicity studies, gene function analysis and drug discovery. Here, we provide a detailed protocol describing how to form HFOs within 14 d. In an initial 4 d preculture period, hPSC aggregates are individually formed in a 96-well format and then Matrigel-embedded. Subsequently, the chemical WNT pathway modulators CHIR99021 and IWP2 are applied, inducing directed differentiation. This highly robust protocol can be used on many different hPSC lines and be combined with manipulation technologies such as gene targeting and drug testing. HFO formation can be assessed by numerous complementary methods, ranging from various imaging approaches to gene expression studies. Here, we highlight the flow cytometry-based analysis of individual HFOs, enabling the quantitative monitoring of lineage formation.
引用
收藏
页码:5652 / 5672
页数:21
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