Key result
Three-dimensional cardiac tissues containing 70% cardiomyocytes, 20% fibroblasts, and 10% endothelial cells demonstrated optimal contractility and sensitive responses to proarrhythmic and inotropic drugs.
Why the study?
It was hypothesized that an appropriate ratio of cardiomyocytes, fibroblasts, endothelial cells, and ECM factors is required to develop three-dimensional cardiac tissues for drug screening systems.
A 3D cardiac tissue model with a 7:2:1 ratio of cardiomyocytes, fibroblasts, and endothelial cells provides an optimized in vitro platform for screening drug-induced cardiotoxicity and arrhythmias.
May refine 3D cardiac tissue models for drug testing; leaves open in vivo and clinical translation.
We hypothesized that an appropriate ratio of cardiomyocytes, fibroblasts, endothelial cells, and extracellular matrix (ECM) factors would be required for the development of three-dimensional cardiac tissues (3D-CTs) as drug screening systems. To verify this hypothesis, ECM-coated human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs), ECM-coated cardiac fibroblasts (CFs), and uncoated cardiac endothelial cells (CEs) were mixed in the following ratios: 10:0:0 (10CT), 7:2:1 (7CT), 5:4:1 (5CT), and 2:7:1 (2CT). The expression of cardiac-, fibroblasts-, and endothelial-specific markers was assessed by FACS, qPCR, and immunostaining while that of ECM-, cell adhesion-, and ion channel-related genes was examined by qPCR. Finally, the contractile properties of the tissues were evaluated in the absence or presence of E-4031 and isoproterenol. The expression of ECM- and adhesion-related genes significantly increased, while that of ion channel-related genes significantly decreased with the CF proportion. Notably, 7CT showed the greatest contractility of all 3D-CTs. When exposed to E-4031 (hERG K channel blocker), 7CT and 5CT showed significantly decreased contractility and increased QT prolongation. Moreover, 10CT and 7CT exhibited a stronger response to isoproterenol than did the other 3D-CTs. Finally, 7CT showed the highest drug sensitivity among all 3D-CTs. In conclusion, 3D-CTs with an appropriate amount of fibroblasts/endothelial cells (7CT in this study) are suitable drug screening systems, e.g. for the detection of drug-induced arrhythmia.
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Takeda et al. (2021) studied Cardiotoxicity screening. 7CT (70% hiPSC-CMs, 20% CFs, 10% CEs) vs. 10CT, 5CT, and 2CT was evaluated on Contractile properties and drug response. Three-dimensional cardiac tissues containing 70% cardiomyocytes, 20% fibroblasts, and 10% endothelial cells demonstrated optimal contractility and sensitive responses to proarrhythmic and inotropic drugs.
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