A patterned human heart tube organoid model generated by pluripotent stem cell self-assembly

类有机物 诱导多能干细胞 生物 心脏发育 干细胞 细胞生物学 间质细胞 电池类型 心肌细胞 转录组 解剖 内科学 细胞 胚胎干细胞 医学 遗传学 癌症研究 基因 基因表达
作者
Brett Volmert,Aitor Aguirre,Ashlin Riggs,Fei Wang,Aniwat Juhong,Artem Kiselev,Aleksandra Kostina,Colin O'Hern,Priyadharshni Muniyandi,Aaron Wasserman,Amanda Huang,Yonatan Lewis-Israeli,Sang-Bum Park,Zhen Qiu,Chao Zhou
标识
DOI:10.1101/2022.12.16.519611
摘要

Abstract Human pluripotent stem cells can recapitulate significant features of mammalian organ development in vitro , including key aspects of heart development. We hypothesized that the organoids thus created can be made substantially more relevant by mimicking aspects of in utero gestation, leading to higher physiological and anatomical resemblance to their in vivo counterparts. Here, we report steps towards generating developmentally inspired maturation methodologies to differentiate early human heart organoids into patterned heart-tube-like structures in a reproducible and high-throughput fashion by complete self-organization. The maturation strategy consists of the controlled and stepwise exposure to metabolic (glucose, fatty acids) and hormonal signals (T3, IGF-1) as present during early heart development. These conditions elicit important transcriptomic, cellular, morphological, metabolomic, and functional changes over a 10-day period consistent with continuously increasing heart complexity, maturation, and patterning. Our data reveals the emergence of atrial and ventricular cardiomyocyte populations, valvular cells, epicardial cells, proepicardial-derived cells, endothelial cells, stromal cells, conductance cells, and cardiac progenitors, all of them cell types present in the primitive heart tube. Anatomically, the organoids elongate and develop well-differentiated atrial and ventricular chambers with compacted myocardial muscle walls and a proepicardial organ. For the first time in a completely self-organizing heart organoid, we show anterior-posterior patterning due to an endogenous retinoic acid gradient originating at the atrial pole, where proepicardial and atrial populations reside, mimicking the developmental process present within the primitive heart tube. Collectively, these findings highlight the ability of self-organization and developmental maturation strategies to recapitulate human heart development. Our patterned human heart tube model constitutes a powerful in vitro tool for dissecting the role of different cell types and genes in human heart development, as well as disease modeling congenital heart defects, and represents a step forward in creating fully synthetic human hearts.
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