类有机物
诱导多能干细胞
胚胎干细胞
心脏发育
生物
干细胞
心脏病
维甲酸
神经科学
生物信息学
细胞生物学
内科学
医学
细胞培养
遗传学
基因
作者
Brett Volmert,Artem Kiselev,Aniwat Juhong,Fei Wang,Ashlin Riggs,Aleksandra Kostina,Colin O’Hern,Priyadharshni Muniyandi,Aaron H. Wasserman,Amanda Huang,Yonatan R. Lewis‐Israeli,Vishal Panda,Sudin Bhattacharya,D. Adam Lauver,Sang‐Bum Park,Zhen Qiu,Chao Zhou,Aitor Aguirre
标识
DOI:10.1038/s41467-023-43999-1
摘要
Abstract Pluripotent stem cell-derived organoids can recapitulate significant features of organ development in vitro. We hypothesized that creating human heart organoids by mimicking aspects of in utero gestation (e.g., addition of metabolic and hormonal factors) would lead to higher physiological and anatomical relevance. We find that heart organoids produced using this self-organization-driven developmental induction strategy are remarkably similar transcriptionally and morphologically to age-matched human embryonic hearts. We also show that they recapitulate several aspects of cardiac development, including large atrial and ventricular chambers, proepicardial organ formation, and retinoic acid-mediated anterior-posterior patterning, mimicking the developmental processes found in the post-heart tube stage primitive heart. Moreover, we provide proof-of-concept demonstration of the value of this system for disease modeling by exploring the effects of ondansetron, a drug administered to pregnant women and associated with congenital heart defects. These findings constitute a significant technical advance for synthetic heart development and provide a powerful tool for cardiac disease modeling.
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