Inactivation-Deficient Human Skeletal Muscle Na + Channels (hNav1.4-L443C/A444W) in Stably Transfected HEK-293 Cells
2004
After transient transfection of an hNav1.4-L443C/A444W mutant clone, HEK-293 cells exhibited large inactivation-deficient Na+ currents. We subsequently established a stable cell line expressing robust inactivation-deficient Na+ currents. Persistent late Na+ currents were far more sensitive to block by class 1 anti-arrhythmic flecainide, mexiletine, propafenone, and amiodarone at 10 μ M than peak Na+ currents. Such results support a hypothesis that persistent late Na+ currents are in vivo targets for class 1 anti-arrhythmic drugs at their therapeutic plasma concentrations. Stably transfected HEK-293 cells expressing robust inactivation-deficient Na+ currents will likely be suitable for screening novel drugs that target persistent late Na+ currents selectively.
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