Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, ON M5S 3E5, Canada.
Division of Cardiology and Peter Munk Cardiac Center, University of Health Network; Toronto, ON M5G 2N2, Canada.
Cell. 2019 Feb 7;176(4):913-927.e18. doi: 10.1016/j.cell.2018.11.042. Epub 2019 Jan 24.
Tissue engineering using cardiomyocytes derived from human pluripotent stem cells holds a promise to revolutionize drug discovery, but only if limitations related to cardiac chamber specification and platform versatility can be overcome. We describe here a scalable tissue-cultivation platform that is cell source agnostic and enables drug testing under electrical pacing. The plastic platform enabled on-line noninvasive recording of passive tension, active force, contractile dynamics, and Ca transients, as well as endpoint assessments of action potentials and conduction velocity. By combining directed cell differentiation with electrical field conditioning, we engineered electrophysiologically distinct atrial and ventricular tissues with chamber-specific drug responses and gene expression. We report, for the first time, engineering of heteropolar cardiac tissues containing distinct atrial and ventricular ends, and we demonstrate their spatially confined responses to serotonin and ranolazine. Uniquely, electrical conditioning for up to 8 months enabled modeling of polygenic left ventricular hypertrophy starting from patient cells.
利用源自人类多能干细胞的心肌细胞进行组织工程学研究有望彻底改变药物发现,但前提是要克服与心脏腔室特化和平台多功能性相关的局限性。我们在这里描述了一种可扩展的组织培养平台,它与细胞来源无关,并且可以在电起搏下进行药物测试。该塑料平台可在线进行非侵入性的被动张力、主动力、收缩动力学和钙瞬变记录,以及动作电位和传导速度的终点评估。通过将定向细胞分化与电场调理相结合,我们构建了具有腔室特异性药物反应和基因表达的电生理上不同的心房和心室组织。我们首次报告了包含明显心房和心室端的异极性心脏组织的工程构建,并证明了它们对 5-羟色胺和雷诺嗪的空间限制反应。独特的是,长达 8 个月的电调理可从患者细胞开始模拟多基因左心室肥厚。