Perspective: mitochondrial STAT3 in cardioprotection

Activation of signal transducer and activator of transcription 3 (STAT3) has been identified as a key cardioprotective signal not only in animal studies but also in humans-in animals, STAT3 is causally involved in cardioprotection. In response to late ischemic conditioning, canonical function of STAT3 activation upregulates the expression of cardioprotective and anti-apoptotic proteins. In its non-canonical function, STAT3 is activated during ischemic conditioning and is part of the cardioprotective cytosolic survival activating factor enhancement pathway. Activated STAT3 is imported and localized to the mitochondria. Mitochondrial STAT3 stimulates the activity of mitochondrial electron transport chain complex I, reduces mitochondrial reactive oxygen species production and mitochondrial permeability transition pore opening. Finally, two novel aspects of STAT activation in cardioprotection are discussed: a genetic variance of the STAT encoding region as a potential primordial confounding variable for cardioprotection, and the cardioprotective potential of sodium-glucose cotransporter 2 inhibitors through STAT3 activation.

Automated summary

Activation of STAT3 has been identified as a key cardioprotective signal, both in animal studies and in humans. It upregulates the expression of cardioprotective and anti-apoptotic proteins and also plays a role in mitochondrial function. Two novel aspects of STAT activation in cardioprotection are discussed: genetic variance as a potential confounding variable and the potential cardioprotective effects of sodium-glucose cotransporter 2 inhibitors.