Preliminary Exam - Kai Chang

Wednesday, November 28, 2018 - 12:00pm to 2:00pm

Title of Defense:
   The role of activin/Daw and mTORC2 signaling in cardiac aging

   Impaired autophagy and mitochondrial quality control have been previously linked to age-related declines of cardiac function. Yet, how those quality control mechanisms are altered during cardiac aging still remains elusive. Here using Drosophila heart as a model system, we show that activin signaling, a member of TGF-beta superfamily, negatively regulates cardiac autophagy and cardiac health during aging. We found that cardiac-specific knockdown of Daw, an activin-like protein in Drosophila, increased cardiac autophagy and prevented age-related cardiac dysfunction, including arrhythmia and bradycardia (slow heart rate). Inhibition of autophagy by Atg1 knockdown blocked Daw knockdown-mediated cardio-protection. Intriguingly, activin signaling genetically interacted with Rictor, the key subunit of mTORC2, to regulate autophagy and cardiac aging. Thus, our findings highlight an emerging role of activin signaling and mTORC2 in the regulation of cardiac homeostasis during aging.