诱导多能干细胞
类有机物
基质凝胶
Wnt信号通路
生物
细胞生物学
药物发现
干细胞
发育生物学
计算生物学
胚胎干细胞
体外
生物信息学
基因
信号转导
遗传学
作者
Lika Drakhlis,Santoshi Biswanath Devadas,Robert Zweigerdt
出处
期刊:Nature Protocols
[Springer Nature]
日期:2021-11-10
卷期号:16 (12): 5652-5672
被引量:29
标识
DOI:10.1038/s41596-021-00629-8
摘要
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.
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