KCNK3 and pulmonary arterial hypertension: The downregulation of voltage potassium channels, notably Kv1.5 [20,21] and TASK-1 [22,23], results in a more depolarized membrane potential in pulmonary arterial smooth muscle cells (PASMC) in PAH patients, leading to increased intracellular calcium and consequently PASMC vasoconstriction and also PASMC proliferation.