Scientific Reports · 2016 · 44 citations · 30 references
EngineeringBioengineeringCell BiologyApoptosisRegenerative MedicineTissue EngineeringCardiac RegenerationCardiac Tissue EngineeringCell CultureCell Culture TechnologyStem Cell BioengineeringTissue Engineering With Stem CellsCardiac Cell ReprogrammingCardiac Cell TherapyCardiac Stem CellsHuman Induced Pluripotent Stem Cell ModelsHuman Stem Cell ModelsInduced Pluripotent Stem CellsProtein Expression LevelsStem Cell-derived Cardiomyocytes
The development of a suitable strategy for eliminating remaining undifferentiated cells is indispensable for the use of human-induced pluripotent stem (iPS) cell-derived cells in regenerative medicine. Here, we show for the first time that TRPV-1 activation through transient culture at 42 °C in combination with agonists is a simple and useful strategy to eliminate iPS cells from bioengineered cardiac cell sheet tissues. When human iPS cells were cultured at 42 °C, almost all cells disappeared by 48 hours through apoptosis. However, iPS cell-derived cardiomyocytes and fibroblasts maintained transcriptional and protein expression levels, and cardiac cell sheets were fabricated after reducing the temperature. TRPV-1 expression in iPS cells was upregulated at 42 °C, and iPS cell death at 42 °C was TRPV-1-dependent. Furthermore, TRPV-1 activation through thermal or agonist treatment eliminated iPS cells in cardiac tissues for a final concentration of 0.4% iPS cell contamination. These findings suggest that the difference in tolerance to TRPV-1 activation between iPS cells and iPS cell-derived cardiac cells could be exploited to eliminate remaining iPS cells in bioengineered cell sheet tissues, which will further reduce the risk of tumour formation.
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