Differential facilitation of N- and P/Q-type calcium channels during trains of action potential-like waveforms

  1. Kevin P M Currie and
  2. Aaron P Fox
  1. Department of Neurobiology, Pharmacology and Physiology, University of Chicago
    947 E. 58th Street, MC 0926, Chicago, IL 60637, USA
  1. Corresponding author
    K. Currie: Department of Neurobiology, Pharmacology and Physiology, University of Chicago, 947 E. 58th Street, MC 0926, Chicago, IL 60637, USA. Email: kevin{at}drugs.bsd.uchicago.edu or aaron{at}arugs.bsd.uchicago.edu

Abstract

Inhibition of presynaptic voltage-gated calcium channels by direct G-protein βγ subunit binding is a widespread mechanism that regulates neurotransmitter release. Voltage-dependent relief of this inhibition (facilitation), most likely to be due to dissociation of the G-protein from the channel, may occur during bursts of action potentials. In this paper we compare the facilitation of N- and P/Q-type Ca2+ channels during short trains of action potential-like waveforms (APWs) using both native channels in adrenal chromaffin cells and heterologously expressed channels in tsA201 cells. While both N- and P/Q-type Ca2+ channels exhibit facilitation that is dependent on the frequency of the APW train, there are important quantitative differences. Approximately 20 % of the voltage-dependent inhibition of N-type ICa was reversed during a train while greater than 40 % of the inhibition of P/Q-type ICa was relieved. Changing the duration or amplitude of the APW dramatically affected the facilitation of N-type channels but had little effect on the facilitation of P/Q-type channels. Since the ratio of N-type to P/Q-type Ca2+ channels varies widely between synapses, differential facilitation may contribute to the fine tuning of synaptic transmission, thereby increasing the computational repertoire of neurons.

Footnotes

    • Received August 27, 2001.
    • Accepted December 10, 2001.
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