Flexible nanoelectronics reveal arrhythmogenesis in transplanted human cardiomyocytes

The transplantation of human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) offers a potential treatment for heart failure, but arrhythmogenic automaticity can arise from these transplanted cells. In this study, we investigated the effects of RADA16, a clinically approved self-assembling peptide that forms nanofibers after injection, on the vascularization, myofibril structure, and electrophysiological adaptation of hiPSC-CMs transplanted into rat hearts. RADA16 accelerated the transition of hiPSC-CMs toward adultlike gene expression profiles, enhanced sarcomere organization, and improved vascularization in the transplanted site. Flexible mesh nanoelectronics revealed fibrillation of transplanted hiPSC-CMs within the beating recipient heart, and RADA16 drastically reduced the automaticity of hiPSC-CMs. Our findings demonstrate the potential of self-assembling nanofibers to advance cardiac cell therapy and how flexible mesh nanoelectronics technology could improve safety.

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Publication Details

Journal
Science
Published
2025-10-16
DOI
https://doi.org/10.1126/science.adw4612
Citations
3
Primary Topic
Neuroscience and Neural Engineering
Type
article
Field-Weighted Citation Impact
2.73
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article

Flexible nanoelectronics reveal arrhythmogenesis in transplanted human cardiomyocytes

Irving Barrera, Anthony Zhu, Richard Lee, Jessica C. Garbern et al.
3 citations
Science
Neuroscience and Neural Engineering
2.73
article

Flexible nanoelectronics reveal arrhythmogenesis in transplanted human cardiomyocytes

Irving Barrera, Anthony Zhu, Richard Lee, Jessica C. Garbern, Elton Aleksi, Nivedhitha Velayutham, Jeffrey J. Saucerman, Morgan Sokol, Junya Aoyama, Fei Chen, Jia Liu, Xinhe Zhang, Pichayathida Luanpaisanon, Eun Seok Gil, Ren Liu, Fang Cao, Hannah Fandl, Satvik Dasariraju, Toshi Amanuma
article en
3 citations

Abstract

The transplantation of human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) offers a potential treatment for heart failure, but arrhythmogenic automaticity can arise from these transplanted cells. In this study, we investigated the effects of RADA16, a clinically approved self-assembling peptide that forms nanofibers after injection, on the vascularization, myofibril structure, and electrophysiological adaptation of hiPSC-CMs transplanted into rat hearts. RADA16 accelerated the transition of hiPSC-CMs toward adultlike gene expression profiles, enhanced sarcomere organization, and improved vascularization in the transplanted site. Flexible mesh nanoelectronics revealed fibrillation of transplanted hiPSC-CMs within the beating recipient heart, and RADA16 drastically reduced the automaticity of hiPSC-CMs. Our findings demonstrate the potential of self-assembling nanofibers to advance cardiac cell therapy and how flexible mesh nanoelectronics technology could improve safety.

ScienceVol. 390(6774)
Broad Institute (US), Boston Children's Hospital (US), Harvard University (US), Matrix Engineering (United States) (US), Matrix Research (United States) (US), University of Virginia (US)
Openalex Percentile: Top 9%
Neuroscience and Neural Engineering
2.73
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