Coupling of Smoothened to inhibitory G proteins reduces voltage-gated K currents in cardiomyocytes and prolongs cardiac action potential duration.

SMO (Smoothened), the central transducer of Hedgehog signaling, is coupled to heterotrimeric G proteins in many cell types, including cardiomyocytes. In this study, we report that activation of SMO with SHH (Sonic Hedgehog) or a small agonist, purmorphamine, rapidly causes a prolongation of the action potential duration that is sensitive to a SMO inhibitor. In contrast, neither of the SMO agonists prolonged the action potential in cardiomyocytes from transgenic GCT/TTA mice, in which G signaling is impaired, suggesting that the effect of SMO is mediated by G proteins. Investigation of the mechanism underlying the change in action potential kinetics revealed that activation of SMO selectively reduces outward voltage-gated K repolarizing (Kv) currents in isolated cardiomyocytes and that it induces a down-regulation of membrane levels of Kv4.3 in cardiomyocytes and intact hearts from WT but not from GiCT/TTA mice. Moreover, perfusion of intact hearts with Shh or purmorphamine increased the ventricular repolarization time (QT interval) and induced ventricular arrhythmias. Our data constitute the first report that acute, noncanonical Hh signaling mediated by G proteins regulates K currents density in cardiomyocytes and sensitizes the heart to the development of ventricular arrhythmias.