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Localization of Presynaptic Plasticity Mechanisms Enables Functional Independence of Synaptic and Ectopic Transmission in the Cerebellum.

Dobson, Katharine L.; Bellamy, Tomas

Authors

Katharine L. Dobson



Abstract

In the cerebellar molecular layer parallel fibre terminals release glutamate from both the active zone and from extrasynaptic “ectopic” sites. Ectopic release mediates transmission to the Bergmann glia that ensheathe the synapse, activating Ca2+-permeable AMPA receptors and glutamate transporters. Parallel fibre terminals exhibit several forms of presynaptic plasticity, including cAMP-dependent long-term potentiation and endocannabinoid-dependent long-term depression, but it is not known whether these presynaptic forms of long-term plasticity also influence ectopic transmission to Bergmann glia. Stimulation of parallel fibre inputs at 16 Hz evoked LTP of synaptic transmission, but LTD of ectopic transmission. Pharmacological activation of adenylyl cyclase by forskolin caused LTP at Purkinje neurons, but only transient potentiation at Bergmann glia, reinforcing the concept that ectopic sites lack the capacity to express sustained cAMP-dependent potentiation. Activation of mGluR1 caused depression of synaptic transmission via retrograde endocannabinoid signalling but had no significant effect at ectopic sites. In contrast, activation of NMDA receptors suppressed both synaptic and ectopic transmission. The results suggest that the signalling mechanisms for presynaptic LTP and retrograde depression by endocannabinoids are restricted to the active zone at parallel fibre synapses, allowing independent modulation of synaptic transmission to Purkinje neurons and ectopic transmission to Bergmann glia.

Citation

Dobson, K. L., & Bellamy, T. (2015). Localization of Presynaptic Plasticity Mechanisms Enables Functional Independence of Synaptic and Ectopic Transmission in the Cerebellum. Neural Plasticity, 2015, https://doi.org/10.1155/2015/602356

Journal Article Type Article
Acceptance Date May 28, 2015
Publication Date Jul 15, 2015
Deposit Date Sep 28, 2017
Publicly Available Date Feb 7, 2019
Print ISSN 2090-5904
Electronic ISSN 1687-5443
Publisher Hindawi Publishing Corporation
Peer Reviewed Peer Reviewed
Volume 2015
Article Number 602356
DOI https://doi.org/10.1155/2015/602356
Public URL https://nottingham-repository.worktribe.com/output/1118714
Publisher URL https://www.hindawi.com/journals/np/2015/602356/
PMID 26171253

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