Na v1.7-Ca 2+ influx-induced increased phosphorylations of extracellular signal-regulated kinase (ERK) and p38 attenuate tau phosphorylation via glycogen synthase kinase-3β: Priming of Na v1.7 gating by ERK and p38

Abstract

In cultured bovine adrenal chromaffin cells expressing Na v1.7 sodium channel isoform, we previously showed that veratridine-induced Na + influx via Na v1.7 and the subsequent Ca 2+ influx via voltage-dependent calcium channels activated protein kinase C-α and Akt, which converged on increasing inhibitory Ser 9-phosphorylation of glycogen synthase kinase-3β, decreasing constitutive Ser 396-phosphorylation of tau. Here, veratridine increased constitutive Tyr 204-phosphorylation of extracellular signal-regulated kinase-1/-2 (ERK1/ERK2) and constitutive Thr 180/Tyr 182-dual phosphorylation of p38 by ∼ 118% (EC 50 = 2.8 μM). Veratridine-induced increased phosphorylation levels of ERK1/ERK2 and p38 were abolished by tetrodotoxin, extracellular Ca 2+ removal, or Gö6976 [12-(2-cyanoethyl)-6,7,12,13-tetrahydro-13-methyl-5-oxo-5H-indolo(2,3-a)pyrrolo(3,4-c)-carbazole;Go6976] (protein kinase C-α inhibitor). PD98059 (2′-amino-3′-methoxyflavone) (ERK1/ERK2 inhibitor) or SB203580 [4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl)1H-imidazole] (p38 inhibitor) attenuated veratridine-induced increased phosphorylation of glycogen synthase kinase-3β and decreased phosphorylation of tau by ∼ 54% and ∼ 56%, as partial blockade by Gö6976. Additionally, basal constitutive phosphorylation levels of ERK1/ERK2 and p38 were decreased by PD98059 or SB203580, but not by SB216763 [3-(2,4-dichlorophenyl)-4-(1-methyl-1H-indolo-3-yl)-1H-pyrrole-2,5-dione] (glycogen synthase kinase-3β inhibitor) or extracellular Ca 2+ removal. In this condition, PD98059 or SB203580 (but not SB216763 or extracellular Ca 2+ removal) inhibited veratridine-induced 22Na + influx and 45Ca 2+ influx, without changing nicotine-induced 22Na + influx via nicotinic receptor-associated cation channels and nicotine-induced 45Ca 2+ influx via voltage-dependent calcium channels. These results suggest that Na v1.7–Ca 2+ influx–protein kinase C-α pathway activated ERK1/ERK2 and p38, which increased phosphorylation of glycogen synthase kinase-3β, decreasing tau phosphorylation. In veratridine-nontreated cells, basal constitutive activities of ERK1/ERK2 and p38 primed Na v1.7 to increase 22Na + influx.