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Conductive electrospun polymer improves stem cell-derived cardiomyocyte function and maturation

Authors :
Gonzalez, Gisselle
Gonzalez, Gisselle
Nelson, Aileena C
Holman, Alyssa R
Whitehead, Alexander J
LaMontagne, Erin
Lian, Rachel
Vatsyayan, Ritwik
Dayeh, Shadi A
Engler, Adam J
Gonzalez, Gisselle
Gonzalez, Gisselle
Nelson, Aileena C
Holman, Alyssa R
Whitehead, Alexander J
LaMontagne, Erin
Lian, Rachel
Vatsyayan, Ritwik
Dayeh, Shadi A
Engler, Adam J
Publication Year :
2023

Abstract

Despite numerous efforts to generate mature human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs), cells often remain immature, electrically isolated, and may not reflect adult biology. Conductive polymers are attractive candidates to facilitate electrical communication between hPSC-CMs, especially at sub-confluent cell densities or diseased cells lacking cell-cell junctions. Here we electrospun conductive polymers to create a conductive fiber mesh and assess if electrical signal propagation is improved in hPSC-CMs seeded on the mesh network. Matrix characterization indicated fiber structure remained stable over weeks in buffer, scaffold stiffness remained near in vivo cardiac stiffness, and electrical conductivity scaled with conductive polymer concentration. Cells remained adherent and viable on the scaffolds for at least 5 days. Transcriptomic profiling of hPSC-CMs cultured on conductive substrates for 3 days showed upregulation of cardiac and muscle-related genes versus non-conductive fibers. Structural proteins were more organized and calcium handling was improved on conductive substrates, even at sub-confluent cell densities; prolonged culture on conductive scaffolds improved membrane depolarization compared to non-conductive substrates. Taken together, these data suggest that blended, conductive scaffolds are stable, supportive of electrical coupling in hPSC-CMs, and promote maturation, which may improve our ability to model cardiac diseases and develop targeted therapies.

Details

Database :
OAIster
Notes :
application/pdf
Publication Type :
Electronic Resource
Accession number :
edsoai.on1449594936
Document Type :
Electronic Resource