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Enhanced Cardiac Differentiation of Human Cardiovascular Disease Patient-Specific Induced Pluripotent Stem Cells by Applying Unidirectional Electrical Pulses Using Aligned Electroactive Nanofibrous Scaffolds
100
Citations
40
References
2017
Year
Tissue EngineeringCardiac MuscleEngineeringBiomaterials DesignCardiac Progenitor CellsBiofabricationCardiac RegenerationBiomedical EngineeringRegenerative MedicineCardiovascular Reparative MedicineEmbryonic HeartInduced Pluripotent Stem CellsMatrix BiologyStem CellsCardiologyVascular Tissue EngineeringElectrical StimulationFunctional Tissue EngineeringEnhanced Cardiac DifferentiationCell EngineeringCell BiologyCardiac ReprogrammingCellular BioengineeringInduced Pluripotent Stem CellStem Cell EngineeringStem Cell ResearchStem-cell TherapyElectrophysiologyCardiovascular PhysiologySinus VenosusMedicineBiomaterialsBiocompatible MaterialEmbryonic Stem CellExtracellular Matrix
In the embryonic heart, electrical impulses propagate in a unidirectional manner from the sinus venosus and appear to be involved in cardiogenesis. In this work, aligned and random polyaniline/polyetersulfone (PANI/PES) nanofibrous scaffolds doped by Camphor-10-sulfonic acid (β) (CPSA) were fabricated via electrospinning and used to conduct electrical impulses in a unidirectional and multidirectional fashion, respectively. A bioreactor was subsequently engineered to apply electrical impulses to cells cultured on PANI/PES scaffolds. We established cardiovascular disease-specific induced pluripotent stem cells (CVD-iPSCs) from the fibroblasts of patients undergoing cardiothoracic surgeries. The CVD-iPSCs were seeded onto the scaffolds, cultured in cardiomyocyte-inducing factors, and exposed to electrical impulses for 1 h/day, over a 15-day time period in the bioreactor. The application of the unidirectional electrical stimulation to the cells significantly increased the number of cardiac Troponin T (cTnT+) cells in comparison to multidirectional electrical stimulation using random fibrous scaffolds. This was confirmed by real-time polymerase chain reaction for cardiac-related transcription factors (NKX2.5, GATA4, and NPPA) and a cardiac-specific structural gene (TNNT2). Here we report for the first time that applying electrical pulses in a unidirectional manner mimicking the unidirectional wave of electrical stimulation in the heart, could increase the derivation of cardiomyocytes from CVD-iPSCs.
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