Key result
Automated 3D hiPSC microtissue screening reliably identifies antiarrhythmic candidates across >2000 compounds.
Why the study?
Current cardiac cell models for drug screening face a trade-off between cellular maturity and throughput, with 3D hiPSC-based models often requiring large cell numbers or complex equipment.
Automated 3D hiPSC-derived cardiac microtissues provide a scalable, reproducible platform for high-throughput cardiac safety and antiarrhythmic drug discovery screening.
May enable scalable mature cardiac microtissue screening; leaves open predictive validity versus existing platforms.
Current cardiac cell models for drug screening often face a trade-off between cellular maturity and throughput. 3D human-induced pluripotent stem cell (hiPSC)-based heart models typically exhibit adult-like features, but their use often requires large cell numbers or complex equipment. In this study, we developed cost-effective methods to scale the production of stem cell-derived cardiac microtissues (cMTs) containing three cardiac cell types and assess calcium transients and action potential metrics for high-throughput screening (HTS). Automating the procedure revealed reproducible drug responsiveness and predictive accuracy in a reference compound screen. Furthermore, an arrhythmic phenotype was reliably triggered in cMTs containing cardiomyocytes with an RYR2 mutation. Screening a library of more than 2000 compounds demonstrated the suitability of the assay for identifying potential antiarrhythmic agents. Our findings underscore the scalability of cMTs and their utility in disease modeling and HTS. The advanced technology readiness level of cMTs supports their regulatory uptake and acceptance within the pharmaceutical industry.
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A 2025 study studied Cardiac safety and drug discovery. 3D hiPSC-cardiac microtissues (cMTs) was evaluated on Calcium transients and action potential metrics for high-throughput screening. Automated production of 3D hiPSC-cardiac microtissues enabled reproducible drug responsiveness and successful screening of over 2000 compounds for potential antiarrhythmic agents.
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