Paredes-Espinosa Maria Belen, Paluh Janet L
Department of Nanoscale Science and Engineering, College of Nanotechnology, Science and Engineering, University at Albany, Albany, NY, United States.
Front Cell Dev Biol. 2025 Jan 28;12:1478549. doi: 10.3389/fcell.2024.1478549. eCollection 2024.
The evolution of stem cell-based heart models from cells and tissues to organoids and assembloids and recently synthetic embryology gastruloids, is poised to revolutionize our understanding of cardiac development, congenital to adult diseases, and patient customized therapies. Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) have already been integrated into transplantable patches and are in preclinical efforts to reverse fibrotic scarring from myocardial infarctions. To inform on the complexity of heart diseases, multi-tissue morphogenic heart models are needed that replicate fundamental components of heart function to heart organogenesis and which require a deep understanding of heart development. Organoid and assembloid models capture selected multicellular cardiac processes, such as chamber formation and priming events for vascularization. Gastruloid heart models offer deeper insights as synthetic embryology to mimic multi-staged developmental events of heart organogenesis including established heart fields, crescent formation and heart tube development along with vascular systemic foundation and even further steps. The human Elongating Multi-Lineage Organized Cardiac (EMLOC) gastruloid model captures these stages and additional events including chamber genesis, patterned vascularization, and extrinsic central and intrinsic cardiac nervous system (CNS-ICNS) integration guided by spatiotemporal and morphogenic processes with neural crest cells. Gastruloid synthetic embryology heart models offer new insights into previously hidden processes of development and provide powerful platforms for addressing heart disease that extends beyond cardiomyocytes, such as arrhythmogenic diseases, congenital defects, and systemic injury interactions, as in spinal cord injuries. The holistic view that is emerging will reveal heart development and disease in unprecedented detail to drive transformative state-of-the-art innovative applications for heart health.
基于干细胞的心脏模型从细胞和组织发展到类器官、组装体,最近又发展到合成胚胎学中的原肠胚样结构,有望彻底改变我们对心脏发育、先天性疾病到成人疾病以及患者定制疗法的理解。人类诱导多能干细胞衍生的心肌细胞(hiPSC-CMs)已经被整合到可移植的贴片之中,并正处于临床前研究阶段,旨在逆转心肌梗死造成的纤维化瘢痕。为了深入了解心脏病的复杂性,需要多组织形态发生心脏模型,这些模型要能复制心脏功能从器官发生到心脏形成的基本组成部分,这就需要对心脏发育有深入的理解。类器官和组装体模型捕捉了选定的多细胞心脏过程,比如腔室形成和血管化的起始事件。原肠胚样心脏模型作为合成胚胎学,能提供更深入的见解,以模拟心脏器官发生的多阶段发育事件,包括已确定的心脏区域、新月形形成和心脏管发育,以及血管系统基础,甚至更远期的步骤。人类伸长多谱系组织化心脏(EMLOC)原肠胚样模型捕捉了这些阶段以及其他事件,包括腔室发生、模式化血管化,以及由神经嵴细胞的时空和形态发生过程引导的外在中枢和内在心脏神经系统(CNS-ICNS)整合。原肠胚样合成胚胎学心脏模型为以前隐藏的发育过程提供了新的见解,并为解决心脏病提供了强大的平台,这些心脏病不仅仅局限于心肌细胞,比如致心律失常疾病、先天性缺陷以及系统性损伤相互作用,如脊髓损伤。正在形成的整体观点将以前所未有的细节揭示心脏发育和疾病,以推动心脏健康领域变革性的前沿创新应用。