Center for Cardiovascular Research, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, Ohio, USA.
The Heart Center, Nationwide Children's Hospital, Columbus, Ohio, USA.
Birth Defects Res. 2022 Oct 1;114(16):959-971. doi: 10.1002/bdr2.1989. Epub 2022 Feb 24.
Single ventricle heart defects (SVHDs) are a severe type of congenital heart disease with poorly understood pathogenic mechanisms. New research using patient-specific induced pluripotent stem cells (iPSCs) as a cellular model is beginning to uncover genetic and cellular etiologies of SVHDs. Hypoplastic left heart syndrome (HLHS) is a type of SVHD that is characterized by an underdeveloped left ventricle and other malformations in the left side of the heart. Hypoplastic right heart syndrome (HRHS), the second type of SVHD, is characterized by an underdeveloped right heart, including malformed tricuspid and pulmonary valves. Despite a noticeable lack of research on SVHD, emerging technologies offer a promising future to further probe the genetic and cellular mechanisms of these diseases. Pediatric cardiovascular research is at the dawn of a new era in terms of what can be discovered with patient-specific iPSCs in conjunction with other technologies (e.g., organoids, single-cell genomics, CRISPR/Cas9 genome editing). In this review, we present recent approaches and findings utilizing patient-specific iPSCs to identify cellular mechanisms responsible for improper cardiac organogenesis in HLHS and HRHS.
单心室心脏缺陷(SVHD)是一种严重的先天性心脏病,其发病机制尚未完全阐明。利用患者特异性诱导多能干细胞(iPSC)作为细胞模型的新研究开始揭示 SVHD 的遗传和细胞病因。左心发育不全综合征(HLHS)是一种 SVHD,其特征是左心室发育不全和心脏左侧的其他畸形。右心发育不全综合征(HRHS)是第二种 SVHD,其特征是右心发育不全,包括三尖瓣和肺动脉瓣畸形。尽管对 SVHD 的研究明显不足,但新兴技术为进一步探究这些疾病的遗传和细胞机制提供了广阔的前景。儿科心血管研究正处于一个新时代的黎明,通过与其他技术(例如类器官、单细胞基因组学、CRISPR/Cas9 基因组编辑)结合使用患者特异性 iPSC 可以发现更多的可能性。在这篇综述中,我们介绍了利用患者特异性 iPSC 来识别 HLHS 和 HRHS 中导致心脏器官发生异常的细胞机制的最新方法和发现。