1Universitätsklinikum Mannheim I. Medizinische Klinik Mannheim, Deutschland; 2University Heart Center Zurich Department of Cardiology Zurich, Schweiz; 3Universitätsmedizin Göttingen Göttingen, Deutschland; 4Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil Medizinische Klinik II, Kardiologie und Angiologie Bochum, Deutschland; 5Ruhr-Universität Bochum Bochum, Deutschland; 6Kath. Klinikum Bochum Cellular Physiology Bochum, Deutschland
Aims: The aim of this study was to assess the pathogenic roles of a novel SLC4A3 variant, c.(1108C>T) p.(Arg370His) in a family with several members showing SQTS, to explore underlying pathomechanism by using patient-specific and CRISPR-engineered human-induced pluripotent stem cell–derived cardiomyocytes (hiPSC-CMs) and gene-edited HEK-293 cells. and to search for possible effective drugs for treatment of the disease.
Methods: hiPSC-CMs from SQTS carrying the variant, from independent healthy donors, and from an isogenic cell line with variant-correction (using CRISPR/Cas9) were employed for this study. In addition, gene-edited HEK-293 cells were generated. Patch-clamp and molecular studies were applied.
Results: The intracellular pH value of SQTS cardiomyocytes was higher compared to healthy donor or isogenic control. CRISPR-insertion of the variant in HEK-293 showed also an increase of intracellular PH value consistent with the SQTS cardiomyocytes. Comparing with hiPSC-CMs from the healthy donors or isogenic controls, cardiomyocytes from the SQTS-patient (SQTS-hiPSC-CMs) displayed abnormal action potentials (APs) with a shortening in the action potential duration (APD) at 50% and 90% of repolarization. To model the SQTS phenotype we increased the intracellular pH value of healthy donor using NH4Cl, which confirmed the finding showing a reduction of APD50 and APD90. In SQTS cardiomyocytes and healthy donors treated with NH4Cl a loss of function of ICa-L, but not of IKr or IKs was observed. The occurrence of arrhythmic events (abnormal spontaneous calcium transients) was increased in SQTS compared to healthy donors or isogenic cells. The total expression level of SLC4A3 was reduced in immunostaining and western blot in SQTS compared to healthy donor or isogenic control. Even more, the SLC4A3 was translocated to the nucleus in SQTS compared to healthy donors and isogenic control cells. The oxidation level was increased in SQTS compared to healthy donors and isogenic cells, whereas the phosphorylation level was reduced. Quinidine prolonged APD50 and APD90 and reduced the arrhythmic events.
Conclusions: The novel SLC4A3 c.(1108C>T) p.(Arg370His) is linked to the clinical phenotype of SQTS. The variant increases the intracellular pH value, increases the oxidation of SLC4A3, reduces the phosphorylation of SLC4A3 and translocate SLC4A3 to the nucleus, leading to ion channel dysfunction and APD-shortening as well as arrhythmias.