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Molecular basis and proarrhythmic role of enhanced small conductance Ca2+ activated K+ channels in patients with atrial fibrillation

Subject Area Pharmacology
Cardiology, Angiology
Term from 2017 to 2022
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 349202494
 
Final Report Year 2023

Final Report Abstract

There remains a significant unmet clinical need for novel safer, more effective antiarrhythmic drugs. Small-conductance Ca2+-activated K+ (SK)-channels show a predominant atrial expression in humans, making them interesting candidates for pharmacological rhythm control of atrial fibrillation (AF). SK-channel inhibitors have significant antiarrhythmic effects in AF animal models, but regulation of SK-channels in AF-patients is poorly understood. Here, we identified a significant upregulation of ISK in atrial cardiomyocytes from cAF-patients and detailed the underlying molecular mechanisms. We provide the first demonstration of AF-associated PP2A upregulation, calmodulin Thr80-dephosphorylation, and PP2A-mediated ISK regulation in human atrial cardiomyocytes. Furthermore, we establish trafficking-dependent upregulation of SK-channel membrane targeting in AF patients as a second factor promoting increased ISK. We present an improved human atrial cardiomyocyte computational model and together with experimental action-potential recordings demonstrate the importance of ISK upregulation for shortening of the atrial effective refractory period. Finally, we revealed a rapid upregulation of plasmalemmal SK2-membrane targeting and ISK after 10 minutes of atrial tachycardia, which is also sensitive to inhibition of PP2A and trafficking pathways. Together, our findings position SK-channels as potentially important contributors to self-promotion of AF in humans, provide novel insight into the molecular control of ISK and provide a mechanistic rationale for the development of SK-channel inhibitors for rhythm control of AF.

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