Apoptosis repressor with caspase domain inhibits cardiomyocyte apoptosis by reducing K+ currents

Department of Medicine, School of Medicine, University of California, San Diego, California 92103 Cell shrinkage is an early prerequisite in programmed cell death, and cytoplasmic K + is a dominant cation that controls intracellular ion homeostasis and cell volume. Blockade of K + channels inhibits apoptotic cell shrinkage and attenuates apoptosis. We examined whether apoptotic repressor with caspase recruitment domain (ARC), an antiapoptotic protein, inhibits cardiomyocyte apoptosis by reducing K + efflux through voltage-gated K + (Kv) channels. In heart-derived H9c2 cells, whole cell Kv currents ( I K(V) ) were isolated by using Ca 2+ -free extracellular (bath) solution and including 5 mM ATP and 10 mM EGTA in the intracellular (pipette) solution. Extracellular application of 5 mM 4-aminopyridine (4-AP), a blocker of Kv channels, reversibly reduced I K(V) by 50-60% in H9c2 cells. The remaining currents during 4-AP treatment may be generated by K + efflux through 4-AP-insensitive K + channels. Overexpression of ARC in heart-derived H9c2 cells significantly decreased I K(V) , whereas treatment with staurosporine, a potent apoptosis inducer, enhanced I K(V) in wild-type cells. The staurosporine-induced increase in I K(V) was significantly suppressed and the staurosporine-mediated apoptosis was markedly inhibited in cells overexpressing ARC compared with cells transfected with the control neomycin vector. These results suggest that the antiapoptotic effect of ARC is, in part, due to inhibition of Kv channels in cardiomyocytes. apoptotic volume decrease; potassium channels; cardiac myocytes * D. Ekhterae, O. Platoshyn, and S. Zhang contributed equally to this work.