Key result
Sublethal activation of caspases with 100 nM staurosporine promoted the generation of cardiomyocytes from mouse embryonic stem cells by stimulating the proliferation and differentiation of c-Kit+/α-actininlow cardiac progenitor cells.
Why the study?
Does sublethal caspase activation promote the generation of cardiomyocytes from mouse embryonic stem cells?
Does sublethal caspase activation promote the generation of cardiomyocytes from mouse embryonic stem cells?
Sublethal caspase activation plays an important role in promoting cardiomyocyte differentiation from embryonic stem cells, suggesting a potential mechanism for cardiac regeneration after injury.
Generation of new cardiomyocytes is critical for cardiac repair following myocardial injury, but which kind of stimuli is most important for cardiomyocyte regeneration is still unclear. Here we explore if apoptotic stimuli, manifested through caspase activation, influences cardiac progenitor up-regulation and cardiomyocyte differentiation. Using mouse embryonic stem cells as a cellular model, we show that sublethal activation of caspases increases the yield of cardiomyocytes while concurrently promoting the proliferation and differentiation of c-Kit+/α-actininlow cardiac progenitor cells. A broad-spectrum caspase inhibitor blocked these effects. In addition, the caspase inhibitor reversed the mRNA expression of genes expressed in cardiomyocytes and their precursors. Our study demonstrates that sublethal caspase-activation has an important role in cardiomyocyte differentiation and may have significant implications for promoting cardiac regeneration after myocardial injury involving exogenous or endogenous cell sources.
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Bulatović et al. (2015) studied Cardiac regeneration. Staurosporine (STS) vs. Vehicle control (DMSO) was evaluated on Cardiomyocyte differentiation (proportion of GFP+ cells and cardiac marker expression). Sublethal activation of caspases with 100 nM staurosporine promoted the generation of cardiomyocytes from mouse embryonic stem cells by stimulating the proliferation and differentiation of c-Kit+/α-actininlow cardiac progenitor cells.
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