PRRT2 Is a Key Component of the Ca2+-Dependent Neurotransmitter Release Machinery
2016
Pierluigi Valente | Enrico Castroflorio | Pia Rossi | Manuela Fadda | Bruno Sterlini | Romina Ines Cervigni | Cosimo Prestigio | Silvia Giovedì | Franco Onofri | Elisa Mura | Fabrizia C. Guarnieri | Antonella Marte | Marta Orlando | Federico Zara | Anna Fassio | Flavia Valtorta | Pietro Baldelli | Anna Corradi | Fabio Benfenati
Heterozygous mutations in proline-rich transmembrane protein 2 (PRRT2) underlie a group of paroxysmal disorders, including epilepsy, kinesigenic dyskinesia, and migraine. Most of the mutations lead to impaired PRRT2 expression, suggesting that loss of PRRT2 function may contribute to pathogenesis. We show that PRRT2 is enriched in presynaptic terminals and that its silencing decreases the number of synapses and increases the number of docked synaptic vesicles at rest. PRRT2-silenced neurons exhibit a severe impairment of synchronous release, attributable to a sharp decrease in release probability and Ca2+ sensitivity and associated with a marked increase of the asynchronous/synchronous release ratio. PRRT2 interacts with the synaptic proteins SNAP-25 and synaptotagmin 1/2. The results indicate that PRRT2 is intimately connected with the Ca2+-sensing machinery and that it plays an important role in the final steps of neurotransmitter release.
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