Differential facilitation of N- and P/Q-type calcium channels during trains of action potential-like waveforms
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, ma...
Gespeichert in:
Veröffentlicht in: | The Journal of physiology 2002-03, Vol.539 (2), p.419-431 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | 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 Ca 2+ 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 Ca 2+ 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 I Ca was reversed during a train while greater than 40 % of the inhibition of P/Q-type I Ca 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 Ca 2+ channels varies widely between synapses, differential facilitation may contribute to the fine tuning of synaptic transmission,
thereby increasing the computational repertoire of neurons. |
---|---|
ISSN: | 0022-3751 1469-7793 |
DOI: | 10.1113/jphysiol.2001.013206 |