Type 1 ryanodine receptor knock-in mutation causing central core disease of skeletal muscle also displays a neuronal phenotype

Abstract

The type 1 ryanodine receptor (RyR1) is expressedwidely in the brain, with high levels in the cerebellum, hippocampus, and hypothalamus. We have shown that L-type Ca2+ channels in terminals of hypothalamic magnocellular neurons are coupled to RyRs, as they are in skeletal muscle, allowing voltage-induced Ca2+ release (VICaR) from internal Ca2+ stores without Ca2+ influx. Here we demonstrate that RyR1 plays a role in VICaR in nerve terminals. Furthermore, in heterozygotes from the Ryr1I4895T/WT (IT/+) mouse line, carrying a knock-in mutation corresponding to one that causes a severe form of human central core disease, VICaR is absent, demonstrating that type 1 RyR mediates VICaR and that thesemice have a neuronal phenotype. The absence of VICaRwas shown in twoways: first, depolarization in the absence of Ca2+ influx elicited Ca 2+syntillas (scintilla, spark, in a nerve terminal, a SYNaptic structure) in WT, but not in mutant terminals; second, in the presence of extracellular Ca2+, IT/+ terminals showed a twofold decrease in global Ca2+ transients, with no change in plasmalemmal Ca 2+ current. Fromthese studieswe drawtwo conclusions: (i) RyR1 plays a role in VICaR in hypothalamic nerve terminals; and (ii) a neuronal alteration accompanies the myopathy in IT/+ mice, and, possibly in humans carrying the corresponding RyR1 mutation.