Abstract
BackgroundWe investigated whether electrical stimulation via indium tin oxide (ITO) could enhance the in vitro culture of neonatal rat ventricular myocytes (NRVMs), which are important in vitro models for studying the mechanisms underlying many aspects of cardiology.MethodsCardiomyocytes were obtained from 1-day-old neonatal rat heart ventricles. To evaluate function of NRVMs cultured on ITO with electrical stimulation, the cell viability, change of cell morphology, immunochemistry using cardiac-specific antibodies, and gene expression were tested.ResultsDefined sarcomeric structure, cell enlargement, and increased distribution of NRVMs appeared in the presence of electrical stimulation. These characteristics were absent in NRVMs cultured under standard culture conditions. In addition, the expression levels of cardiomyocyte-specific and ion channel markers were higher in NRVMs seeded on ITO-coated dishes than in the control group at 14 days after seeding. ITO-coated dishes could effectively provide electrical cues to support the in vitro culture of NRVMs.ConclusionsThese results provide supporting evidence that electrical stimulation via ITO can be effectively used to maintain culture and enhance function of cardiomyocytes in vitro.
Highlights
We investigated whether electrical stimulation via indium tin oxide (ITO) could enhance the in vitro culture of neonatal rat ventricular myocytes (NRVMs), which are important in vitro models for studying the mechanisms underlying many aspects of cardiology
NRVM isolation and electrical stimulation Cardiomyocytes were obtained from 1-day-old neonatal rat heart ventricles
A total of 5 × 104 cells was seeded onto an uncoated glass slide and an ITO-coated slide and cultured in DMEM supplemented with 10% FCS for 3 days
Summary
We investigated whether electrical stimulation via indium tin oxide (ITO) could enhance the in vitro culture of neonatal rat ventricular myocytes (NRVMs), which are important in vitro models for studying the mechanisms underlying many aspects of cardiology. Cardiomyocytes hardly proliferate after birth but grow as individual cells to display functionally and structurally mature phenotypes [11, 12]. These cells have membranes which allow sodium, calcium, potassium ions to slowly move inward and out the cell for systole and diastole [10]. To support these characteristics in vitro, appropriate conditions are
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