Synthetic embryology of the human heart.

IF 4.6 2区 生物学 Q2 CELL BIOLOGY Frontiers in Cell and Developmental Biology Pub Date : 2025-01-28 eCollection Date: 2024-01-01 DOI:10.3389/fcell.2024.1478549
Maria Belen Paredes-Espinosa, Janet L Paluh
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Abstract

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 in vitro 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 in vivo 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.

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人类心脏的合成胚胎学。
基于干细胞的心脏模型从细胞和组织到类器官和集合体,以及最近合成的胚胎学类原肠细胞的进化,将彻底改变我们对心脏发育、先天性到成人疾病以及患者定制治疗的理解。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中,并且正在进行临床前研究,以逆转心肌梗死引起的纤维化瘢痕。为了了解心脏疾病的复杂性,需要建立多组织形态发生的心脏模型,将心脏功能的基本组成部分复制到体外心脏器官发生中,这需要对心脏发育有深入的了解。类器官和集合体模型捕获了选定的多细胞心脏过程,如腔室形成和血管形成的启动事件。胃原体心脏模型作为合成胚胎学提供了更深入的见解,以模拟体内心脏器官发生的多阶段发育事件,包括建立心脏区,新月形成和心脏管的发育以及血管系统的基础,甚至进一步的步骤。人类长形多谱系有组织心脏(EMLOC)胃原体模型捕获了这些阶段和其他事件,包括腔室发生、血管形成化、外源性中枢和内在心脏神经系统(CNS-ICNS)整合,这些过程由神经嵴细胞的时空和形态发生过程引导。胃原体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,并为解决心肌细胞以外的心脏病提供了强大的平台,如心律失常疾病、先天性缺陷和全身损伤相互作用,如脊髓损伤。正在出现的整体观点将以前所未有的细节揭示心脏发展和疾病,以推动心脏健康的变革性最新创新应用。
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来源期刊
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
9.70
自引率
3.60%
发文量
2531
审稿时长
12 weeks
期刊介绍: Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board. The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology. With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.
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