Protein kinase A mediates voltage-dependent facilitation of Ca2+ current in presynaptic hair cells in Hermissenda crassicornis

Catherine T. Tamse, Yanfang Xu, Haitao Song, Liping Nie, Ebenezer N. Yamoah

Research output: Contribution to journalArticle

9 Scopus citations

Abstract

The simplest cellular model for classical conditioning in the nudibranch mollusk, Hermissenda crassicornis, involves the presynaptic hair cells and postsynaptic photoreceptors. Whereas the cellular mechanisms for postsynaptic photoreceptors have been studied extensively, the presynaptic mechanisms remain uncertain. Here, we determined the phenotype of the voltage-dependent Ca2+ current in the presynaptic hair cells that may be directly involved in changes in synaptic efficacy during classical conditioning. The Ca2+ current can be classified as a P-type current because its activation voltage under seawater recording conditions is approximately -30 mV, it showed slow inactivation, and it is reversibly blocked by ω-agatoxin-IVA. The steady-state activation and inactivation curves revealed a window current, and the single-channel conductance is approximately 20 pS. The P-type current was enhanced by cAMP analogs (approximately 1.3-fold), and by forskolin, an activator of adenylyl cyclase (approximately 1.25-fold). In addition, the P-type current showed voltage-dependent facilitation, which is mediated by protein kinase A (PKA). Specifically, the PKA inhibitor peptide [PKI(6-22)amide] blocked the enhancement of the Ca2+ current produced by conditioning depolarization prepulses. Because neurotransmitter release is mediated by Ca2+ influx via voltage-gated Ca2+ channels, and because of the nonlinear relationship between the Ca2+ influx and neurotransmitter release, we propose that voltage-dependent facilitation of the P-type current in hair cells would produce a robust change in synaptic efficacy.

Original languageEnglish (US)
Pages (from-to)1718-1726
Number of pages9
JournalJournal of Neurophysiology
Volume89
Issue number3
DOIs
StatePublished - Mar 1 2003

ASJC Scopus subject areas

  • Physiology
  • Neuroscience(all)

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