Tampakakis Emmanouil, Miyamoto Matthew, Kwon Chulan
Division of Cardiology, Department Medicine, Johns Hopkins School of Medicine.
Division of Cardiology, Department Medicine, Johns Hopkins School of Medicine;
J Vis Exp. 2019 Jul 3(149). doi: 10.3791/59826.
Pluripotent stem cells offer great potential for understanding heart development and disease and for regenerative medicine. While recent advances in developmental cardiology have led to generating cardiac cells from pluripotent stem cells, it is unclear if the two cardiac fields - the first and second heart fields (FHF and SHF) - are induced in pluripotent stem cells systems. To address this, we generated a protocol for in vitro specification and isolation of heart field-specific cardiac progenitor cells. We used embryonic stem cells lines carrying Hcn4-GFP and Tbx1-Cre; Rosa-RFP reporters of the FHF and the SHF, respectively, and live cell immunostaining of the cell membrane protein Cxcr4, a SHF marker. With this approach, we generated progenitor cells which recapitulate the functional properties and transcriptome of their in vivo counterparts. Our protocol can be utilized to study early specification and segregation of the two heart fields and to generate chamber-specific cardiac cells for heart disease modelling. Since this is an in vitro organoid system, it may not provide precise anatomical information. However, this system overcomes the poor accessibility of gastrulation-stage embryos and can be upscaled for high-throughput screens.
多能干细胞在理解心脏发育与疾病以及再生医学方面具有巨大潜力。虽然发育心脏病学的最新进展已实现从多能干细胞生成心脏细胞,但尚不清楚在多能干细胞系统中是否能诱导出两个心脏区域——第一和第二心脏区域(FHF和SHF)。为解决这一问题,我们制定了一种体外定向分化和分离心脏区域特异性心脏祖细胞的方案。我们使用了分别携带FHF和SHF的Hcn4-GFP和Tbx1-Cre;Rosa-RFP报告基因的胚胎干细胞系,并对细胞膜蛋白Cxcr4(一种SHF标记物)进行活细胞免疫染色。通过这种方法,我们生成了祖细胞,其重现了体内对应细胞的功能特性和转录组。我们的方案可用于研究两个心脏区域的早期定向分化和分离,并生成用于心脏病建模的特定腔室心脏细胞。由于这是一个体外类器官系统,它可能无法提供精确的解剖信息。然而,该系统克服了原肠胚形成期胚胎难以获取的问题,并且可以扩大规模用于高通量筛选。