Abstract
Cardiac constructs fabricated using human induced pluripotent stem cells-derived cardiomyocytes (iPSCs-CMs) are useful for evaluating the cardiotoxicity of and cardiac response to new drugs. Previously, we fabricated scaffold-free three-dimensional (3D) tubular cardiac constructs using a bio-3D printer, which can load cardiac spheroids onto a needle array. In this study, we developed a method to measure the contractile force and to evaluate the drug response in cardiac constructs. Specifically, we measured the movement of the needle tip upon contraction of the cardiac constructs on the needle array. The contractile force and beating rate of the cardiac constructs were evaluated by analysing changes in the movement of the needle tip. To evaluate the drug response, contractile properties were measured following treatment with isoproterenol, propranolol, or blebbistatin, in which the movement of the needle tip was increased following isoproterenol treatment, but was decreased following propranolol or blebbistain, treatments. To evaluate cardiotoxicity, contraction and cell viability of the cardiac constructs were measured following doxorubicin treatment. Cell viability was found to decrease with decreasing movement of the needle tip following doxorubicin treatment. Collectively, our results show that this method can aid in evaluating the contractile force of cardiac constructs.
Highlights
Cardiac constructs fabricated using human induced pluripotent stem cells-derived cardiomyocytes are useful for evaluating the cardiotoxicity of and cardiac response to new drugs
A system to evaluate the 3D contractile force of cardiac constructs is important for new drug development
Cardiomyocytes in the cardiac constructs were rearranged to the outer surface of the constructs after cultivation
Summary
Cardiac constructs fabricated using human induced pluripotent stem cells-derived cardiomyocytes (iPSCs-CMs) are useful for evaluating the cardiotoxicity of and cardiac response to new drugs. In preclinical studies to develop new drugs, many researchers have used the two-dimensional (2D) monolayer cardiomyocyte culture as a conventional method to evaluate drug response and cardiotoxicity[6,7,8,9]. This method can measure the field potential duration and action potential of each cardiomyocyte using multi-electrode arrays and the contraction of cardiomyocytes using movie analysis software. We report a method to analyse the movement of the needle tip as an indicator of contractile force in cardiac constructs on a needle array, as well as the drug response and cardiotoxicity of cardiac constructs
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