Yu Brian, Zhao Shane Rui, Yan Christopher D, Zhang Mao, Wu Joseph C
Stanford Cardiovascular Institute, Stanford University, Stanford, CA, 94503, USA.
Division of Cardiovascular Medicine, Department of Medicine, Stanford University, Stanford, CA, USA.
Curr Cardiol Rep. 2022 May;24(5):487-496. doi: 10.1007/s11886-022-01670-z. Epub 2022 Mar 4.
Induced pluripotent stem cells (iPSCs) have become widely adopted tools in cardiovascular biology due to their ability to differentiate into patient-specific cell types. Here, we describe the current protocols, important discoveries, and experimental limitations from the iPSC-derived cell types of the human heart: cardiomyocytes, cardiac fibroblasts, vascular smooth muscle cells, endothelial cells, and pericytes. In addition, we also examine the progress of 3D-based cell culture systems.
There has been rapid advancement in methods to generate cardiac iPSC-derived cell types. These advancements have led to improved cardiovascular disease modeling, elucidation of interactions among different cell types, and the creation of 3D-based cell culture systems able to provide more physiologically relevant insights into cardiovascular diseases. iPSCs have become an instrumental model system in the toolbox of cardiovascular biologists. Ongoing research continues to advance the use of iPSCs in (1) disease modeling, (2) drug screening, and (3) clinical trials in a dish.
诱导多能干细胞(iPSC)因其能够分化为患者特异性细胞类型,已成为心血管生物学中广泛应用的工具。在此,我们描述了从人心脏的iPSC衍生细胞类型(心肌细胞、心脏成纤维细胞、血管平滑肌细胞、内皮细胞和周细胞)中获得的当前方案、重要发现和实验局限性。此外,我们还研究了基于3D的细胞培养系统的进展。
生成心脏iPSC衍生细胞类型的方法取得了快速进展。这些进展促进了心血管疾病建模的改进、不同细胞类型之间相互作用的阐明,以及基于3D的细胞培养系统的创建,这些系统能够为心血管疾病提供更具生理相关性的见解。iPSC已成为心血管生物学家工具库中的一个重要模型系统。正在进行的研究继续推动iPSC在(1)疾病建模、(2)药物筛选和(3)体外临床试验中的应用。