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Title: Functional compensation of P/Q by N-type channels blocks short-term plasticity at the calyx of Held presynaptic terminal
Authors: González Inchauspe, C.
Martini, F. J.
Uchitel, O. D.
Forsythe, Ian D.
First Published: 17-Nov-2004
Publisher: Society for Neuroscience
Citation: Journal of Neuroscience, 2004, 24 (46), pp. 10379-10383
Abstract: Calcium channels of the P/Q subtype mediate transmitter release at the neuromuscular junction and at many central synapses, such as the calyx of Held. Transgenic mice in which α1A channels are ablated provide a powerful tool with which to test compensatory mechanisms at the synapse and to explore mechanisms of presynaptic regulation associated with expression of P/Q channels. Using the calyx of Held preparation from the knock-out (KO) mice, we show here that N-type channels functionally compensate for the absence of P/Q subunits at the calyx and evoke giant synaptic currents [approximately two-thirds of the magnitude of wild-type (WT) responses]. However, although evoked paired-pulse facilitation is prominent in WT, this facilitation is greatly diminished in the KO. In addition, direct recording of presynaptic calcium currents revealed that the major functional difference was the absence of calcium-dependent facilitation at the calyx in the P/Q KO animals. We conclude that one physiological function of P/Q channels is to provide additional facilitatory drive, so contributing to maintenance of transmission as vesicles are depleted during high throughput synaptic transmission.
DOI Link: 10.1523/JNEUROSCI.2104-04.2004
ISSN: 0270-6474
eISSN: 1529-2401
Type: Journal Article
Rights: Creative Commons Attribution License
Appears in Collections:Published Articles, Dept. of Cell Physiology and Pharmacology

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