Center for Cardiovascular Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
Heart Center, Nationwide Children's Hospital, Columbus, OH, USA.
Birth Defects Res. 2022 Oct 1;114(16):926-947. doi: 10.1002/bdr2.1999. Epub 2022 Mar 9.
Congenital heart disease (CHD) represents a major class of birth defects worldwide and is associated with cardiac malformations that often require surgical intervention immediately after birth. Despite the intense efforts from multicentric genome/exome sequencing studies that have identified several genetic variants, the etiology of CHD remains diverse and often unknown. Genetically modified animal models with candidate gene deficiencies continue to provide novel molecular insights that are responsible for fetal cardiac development. However, the past decade has seen remarkable advances in the field of human induced pluripotent stem cell (hiPSC)-based disease modeling approaches to better understand the development of CHD and discover novel preventative therapies. The iPSCs are derived from reprogramming of differentiated somatic cells to an embryonic-like pluripotent state via overexpression of key transcription factors. In this review, we describe how differentiation of hiPSCs to specialized cardiac cellular identities facilitates our understanding of the development and pathogenesis of CHD subtypes. We summarize the molecular and functional characterization of hiPSC-derived differentiated cells in support of normal cardiogenesis, those that go awry in CHD and other heart diseases. We illustrate how stem cell-based disease modeling enables scientists to dissect the molecular mechanisms of cell-cell interactions underlying CHD. We highlight the current state of hiPSC-based studies that are in the verge of translating into clinical trials. We also address limitations including hiPSC-model reproducibility and scalability and differentiation methods leading to cellular heterogeneity. Last, we provide future perspective on exploiting the potential of hiPSC technology as a predictive model for patient-specific CHD, screening pharmaceuticals, and provide a source for cell-based personalized medicine. In combination with existing clinical and animal model studies, data obtained from hiPSCs will yield further understanding of oligogenic, gene-environment interaction, pathophysiology, and management for CHD and other genetic cardiac disorders.
先天性心脏病(CHD)是全球范围内主要的出生缺陷类型之一,与心脏畸形有关,这些心脏畸形通常需要在出生后立即进行手术干预。尽管多中心基因组/外显子测序研究已经确定了几种遗传变异,但 CHD 的病因仍然多种多样,而且常常是未知的。具有候选基因缺失的基因修饰动物模型继续提供新的分子见解,这些见解负责胎儿心脏发育。然而,在过去的十年中,基于人诱导多能干细胞(hiPSC)的疾病建模方法领域取得了显著进展,以更好地理解 CHD 的发展并发现新的预防疗法。iPSCs 是通过过表达关键转录因子将分化的体细胞重编程为胚胎样多能状态而获得的。在这篇综述中,我们描述了 hiPSC 向特化的心脏细胞表型分化如何促进我们对 CHD 亚型的发育和发病机制的理解。我们总结了 hiPSC 衍生的分化细胞的分子和功能特征,以支持正常的心脏发生,以及在 CHD 和其他心脏疾病中出错的细胞。我们说明了基于干细胞的疾病建模如何使科学家能够剖析 CHD 中细胞-细胞相互作用的分子机制。我们强调了基于 hiPSC 的研究的当前状态,这些研究即将转化为临床试验。我们还解决了包括 hiPSC 模型的可重复性和可扩展性以及导致细胞异质性的分化方法在内的局限性。最后,我们提供了利用 hiPSC 技术作为预测模型用于患者特异性 CHD、筛选药物的未来展望,并为基于细胞的个性化医疗提供了来源。与现有的临床和动物模型研究相结合,从 hiPSC 获得的数据将进一步了解多基因、基因-环境相互作用、病理生理学以及 CHD 和其他遗传性心脏疾病的管理。