Development of low-cost electrical stimulation device to promote hiPSC-CM differentiation and functionality

Human induced pluripotent stem cell differentiated cardiomyocytes (hiPSC-CMs) hold great potential to resolve cardiovascular disease but are stymied by their functional immaturity. The complex electric potentials measured during cardiogenesis point to the potential of exogenous electrical stimulation in improving cardiac differentiation and functionality. Herein, we create, validate, and implement a low-cost electrical stimulation device to stimulate human induced pluripotent stem cells during cardiac differentiation. Notably, our open-source device enables the generation of dynamic electrical stimulation regimens that may vary in frequency and pulse duration over time. Our results show that cardiac differentiation under dynamic electrical stimulation improves cardiac differentiation efficiency, beating synchronicity, and intracellular calcium handling and flow but impedes contraction compared to static electrical stimulation and no stimulation controls. We also show that pulse duration is an important stimulation parameter to optimize for hiPSC-CM differentiation and functionality. Across nearly all measured metrics, hiPSC-CMs subjected to dynamic pulse duration stimulation during differentiation outperformed those generated under dynamic frequency stimulation. We anticipate that more complex dynamic electrical stimulation regimens may be generated to further optimize hiPSC-CM functionality and maturity.

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Publication Details

Journal
APL Bioengineering
Published
2026-01-02
DOI
https://doi.org/10.1063/5.0269538
Primary Topic
Planarian Biology and Electrostimulation
Type
article
Field-Weighted Citation Impact
0.00

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article

Development of low-cost electrical stimulation device to promote hiPSC-CM differentiation and functionality

Janet Zoldan, Nikhith Kalkunte, Talia E. Delambre, Amy Brock et al.
APL Bioengineering
Planarian Biology and Electrostimulation
article

Development of low-cost electrical stimulation device to promote hiPSC-CM differentiation and functionality

Janet Zoldan, Nikhith Kalkunte, Talia E. Delambre, Amy Brock, Nima Momtahan, Sogu Sohn, Cody Callahan, Sarah Meng
article en

Abstract

Human induced pluripotent stem cell differentiated cardiomyocytes (hiPSC-CMs) hold great potential to resolve cardiovascular disease but are stymied by their functional immaturity. The complex electric potentials measured during cardiogenesis point to the potential of exogenous electrical stimulation in improving cardiac differentiation and functionality. Herein, we create, validate, and implement a low-cost electrical stimulation device to stimulate human induced pluripotent stem cells during cardiac differentiation. Notably, our open-source device enables the generation of dynamic electrical stimulation regimens that may vary in frequency and pulse duration over time. Our results show that cardiac differentiation under dynamic electrical stimulation improves cardiac differentiation efficiency, beating synchronicity, and intracellular calcium handling and flow but impedes contraction compared to static electrical stimulation and no stimulation controls. We also show that pulse duration is an important stimulation parameter to optimize for hiPSC-CM differentiation and functionality. Across nearly all measured metrics, hiPSC-CMs subjected to dynamic pulse duration stimulation during differentiation outperformed those generated under dynamic frequency stimulation. We anticipate that more complex dynamic electrical stimulation regimens may be generated to further optimize hiPSC-CM functionality and maturity.

APL BioengineeringVol. 10(1)
The University of Texas at Austin (US)
National Science Foundation, University of Texas at Austin, National Institutes of Health, Graduate School, University of Texas, Austin
Openalex Percentile: Top 99%
Planarian Biology and Electrostimulation
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