Reilly Louise, Munawar Saba, Zhang Jianhua, Crone Wendy C, Eckhardt Lee L
Cellular and Molecular Arrhythmia Research Program, Division of Cardiovascular Medicine, Department of Medicine, University of Wisconsin-Madison, Madison, WI, United States.
Department of Engineering Physics, College of Engineering, University of Wisconsin-Madison, Madison, WI, United States.
Front Cardiovasc Med. 2022 Aug 12;9:966094. doi: 10.3389/fcvm.2022.966094. eCollection 2022.
Disease modeling using human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) has both challenges and promise. While patient-derived iPSC-CMs provide a unique opportunity for disease modeling with isogenic cells, the challenge is that these cells still demonstrate distinct properties which make it functionally less akin to adult cardiomyocytes. In response to this challenge, numerous innovations in differentiation and modification of hiPSC-CMs and culture techniques have been developed. Here, we provide a focused commentary on hiPSC-CMs for use in disease modeling, the progress made in generating electrically and metabolically mature hiPSC-CMs and enabling investigative platforms. The solutions are bringing us closer to the promise of modeling heart disease using human cells .
利用人诱导多能干细胞衍生的心肌细胞(hiPSC-CMs)进行疾病建模既面临挑战也充满希望。虽然患者来源的iPSC-CMs为使用同基因细胞进行疾病建模提供了独特机会,但挑战在于这些细胞仍表现出不同特性,使其在功能上与成年心肌细胞不太相似。针对这一挑战,人们在hiPSC-CMs的分化、修饰及培养技术方面进行了大量创新。在此,我们重点评论用于疾病建模的hiPSC-CMs、在生成电生理和代谢成熟的hiPSC-CMs以及建立研究平台方面所取得的进展。这些解决方案正使我们更接近利用人类细胞对心脏病进行建模的前景。