Abstract
The target of rapamycin (TOR) kinase is part of an evolutionarily conserved signaling pathway that coordinates cell growth, survival, and autophagy. Previously, pharmacological studies using rapamycin have suggested a cardioprotective effect of TOR signaling inhibition on cardiomyopathy. We found that rapamycin exerts a conserved cardioprotective effect in two adult zebrafish models of cardiomyopathy of different etiology, and provided the first genetic evidence to support a long-term cardioprotective effect of TOR signaling inhibition. Moreover, we detected dynamic TOR-autophagy activities along different stages of cardiomyopathy. This needs to be considered when developing TOR-autophagy-based therapeutics for cardiomyopathy. © 2011 Landes Bioscience.
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Ding, Y., Sun, X., & Xu, X. (2012). TOR-autophagy signaling in adult zebrafish models of cardiomyopathy. Autophagy. Taylor and Francis Inc. https://doi.org/10.4161/auto.8.1.18536
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