SK4 K+ channels are therapeutic targets for the treatment of cardiac arrhythmias. Issue 4 (20th February 2017)

• Record Type: Journal Article
• Authors: Haron‐Khun, Shiraz; Weisbrod, David; Bueno, Hanna; Yadin, Dor; Behar, Joachim; Peretz, Asher; Binah, Ofer; Hochhauser, Edith; Eldar, Michael; Yaniv, Yael; Arad, Michael; Attali, Bernard
• Is Part Of: EMBO molecular medicine. Volume 9:Issue 4(2017)
• Page Start: 415
• Page End: 429
• Publication Date: 2017-02-20
• Subjects: cardiac arrhythmia -- catecholaminergic polymorphic ventricular tachycardia -- pacemaker -- potassium channel -- SK4; Molecular biology -- Periodicals; Medical genetics -- Periodicals; Pathology, Molecular -- Periodicals; 616.04205
• DOI: 10.15252/emmm.201606937
• Languages: English
• ISSNs: 1757-4676

Abstract

Abstract: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a stress‐provoked ventricular arrhythmia, which also manifests sinoatrial node (SAN) dysfunction. We recently showed that SK4 calcium‐activated potassium channels are important for automaticity of cardiomyocytes derived from human embryonic stem cells. Here SK4 channels were identified in human induced pluripotent stem cell‐derived cardiomyocytes (hiPSC‐CMs) from healthy and CPVT2 patients bearing a mutation in calsequestrin 2 (CASQ2‐D307H) and in SAN cells from WT and CASQ2‐D307H knock‐in (KI) mice. TRAM‐34, a selective blocker of SK4 channels, prominently reduced delayed afterdepolarizations and arrhythmic Ca 2+ transients observed following application of the β‐adrenergic agonist isoproterenol in CPVT2‐derived hiPSC‐CMs and in SAN cells from KI mice. Strikingly, in vivo ECG recording showed that intraperitoneal injection of the SK4 channel blockers, TRAM‐34 or clotrimazole, greatly reduced the arrhythmic features of CASQ2‐D307H KI and CASQ2 knockout mice at rest and following exercise. This work demonstrates the critical role of SK4 Ca 2+ ‐activated K + channels in adult pacemaker function, making them promising therapeutic targets for the treatment of cardiac ventricular arrhythmias such as CPVT. Synopsis: SK4 Ca 2+ ‐activated K + channels are important for embryonic cardiac pacemaker function, and are now found to be crucial for adult sinoatrial node (SAN) pacing and successfully targeted for treatment of cardiac arrhythmias in mice. Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited stress‐provoked ventricular arrhythmia, which also manifests sinoatrial node dysfunction. SK4 channels are identified in hiPSC cardiomyocytes (CMs) from healthy and CPVT2 patients and in SAN cells from WT and CASQ2‐D307H knock‐in (KI) mice. The SK4 channel blocker TRAM‐34 reduces the arrhythmic Ca 2+ transients observed in CPVT2‐derived hiPSC‐CMs and in SAN cells from KI mice. TRAM‐34 prominently decreased the ECG arrhythmic features of CASQ2‐D307H KI and CASQ2 knockout mice. SK4 channels are promising therapeutic targets for the treatment of cardiac arrhythmias such as CPVT. Abstract : SK4 Ca 2+ ‐activated K + channels are important for embryonic cardiac pacemaker function, and are now found to be crucial for adult sinoatrial node (SAN) pacing and successfully targeted for treatment of cardiac arrhythmias in mice.