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Distribution of vesicle pools in cerebellar parallel fibre terminals after depression of ectopic transmission

At parallel fibre terminals in the cerebellar cortex, glutamate released outside of the active zone can activate AMPA receptors on juxtaposed Bergmann glial cell processes. This process is termed “ectopic” release, and allows for directed transmission to astroglial cells that is functionally indepen...

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Detalles Bibliográficos
Autores principales: Dobson, Katharine L., Smith, Zoe H., Bellamy, Tomas C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053221/
https://www.ncbi.nlm.nih.gov/pubmed/30024947
http://dx.doi.org/10.1371/journal.pone.0200937
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author Dobson, Katharine L.
Smith, Zoe H.
Bellamy, Tomas C.
author_facet Dobson, Katharine L.
Smith, Zoe H.
Bellamy, Tomas C.
author_sort Dobson, Katharine L.
collection PubMed
description At parallel fibre terminals in the cerebellar cortex, glutamate released outside of the active zone can activate AMPA receptors on juxtaposed Bergmann glial cell processes. This process is termed “ectopic” release, and allows for directed transmission to astroglial cells that is functionally independent of synaptic transmission to postsynaptic Purkinje neurons. The location of ectopic sites in presynaptic terminals is uncertain. Functional evidence suggests that stimulation of parallel fibres at 1 Hz exhausts ectopic transmission due to a failure to rapidly recycle vesicles to the ectopic pool, and so would predict a loss of vesicles in the near vicinity of extrasynaptic glial processes. In this study we used this stimulation protocol to investigate whether the distribution of vesicles within the presynaptic terminal is altered after suppression of ectopic release. Stimulation at 1 Hz had only a minor impact on the distribution of vesicles in presynaptic terminals when analysed with electron microscopy. Vesicle number and terminal size were unaffected by 1 Hz stimulation, but the relative abundance of vesicles in close proximity to the active zone was marginally reduced. In contrast, the fraction of vesicles facing glial membranes was unchanged after suppression of ectopic transmission. 1 Hz stimulation also resulted in a small but statistically-significant increase in the distance between glial membrane and presynaptic terminal, suggesting withdrawal of glial membranes from synapses is detectable in ultrastructural anatomy within minutes. These results raise doubts about the location of ectopic release sites, but indicate that neuron-glial association varies on a dynamic time scale.
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spelling pubmed-60532212018-07-27 Distribution of vesicle pools in cerebellar parallel fibre terminals after depression of ectopic transmission Dobson, Katharine L. Smith, Zoe H. Bellamy, Tomas C. PLoS One Research Article At parallel fibre terminals in the cerebellar cortex, glutamate released outside of the active zone can activate AMPA receptors on juxtaposed Bergmann glial cell processes. This process is termed “ectopic” release, and allows for directed transmission to astroglial cells that is functionally independent of synaptic transmission to postsynaptic Purkinje neurons. The location of ectopic sites in presynaptic terminals is uncertain. Functional evidence suggests that stimulation of parallel fibres at 1 Hz exhausts ectopic transmission due to a failure to rapidly recycle vesicles to the ectopic pool, and so would predict a loss of vesicles in the near vicinity of extrasynaptic glial processes. In this study we used this stimulation protocol to investigate whether the distribution of vesicles within the presynaptic terminal is altered after suppression of ectopic release. Stimulation at 1 Hz had only a minor impact on the distribution of vesicles in presynaptic terminals when analysed with electron microscopy. Vesicle number and terminal size were unaffected by 1 Hz stimulation, but the relative abundance of vesicles in close proximity to the active zone was marginally reduced. In contrast, the fraction of vesicles facing glial membranes was unchanged after suppression of ectopic transmission. 1 Hz stimulation also resulted in a small but statistically-significant increase in the distance between glial membrane and presynaptic terminal, suggesting withdrawal of glial membranes from synapses is detectable in ultrastructural anatomy within minutes. These results raise doubts about the location of ectopic release sites, but indicate that neuron-glial association varies on a dynamic time scale. Public Library of Science 2018-07-19 /pmc/articles/PMC6053221/ /pubmed/30024947 http://dx.doi.org/10.1371/journal.pone.0200937 Text en © 2018 Dobson et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dobson, Katharine L.
Smith, Zoe H.
Bellamy, Tomas C.
Distribution of vesicle pools in cerebellar parallel fibre terminals after depression of ectopic transmission
title Distribution of vesicle pools in cerebellar parallel fibre terminals after depression of ectopic transmission
title_full Distribution of vesicle pools in cerebellar parallel fibre terminals after depression of ectopic transmission
title_fullStr Distribution of vesicle pools in cerebellar parallel fibre terminals after depression of ectopic transmission
title_full_unstemmed Distribution of vesicle pools in cerebellar parallel fibre terminals after depression of ectopic transmission
title_short Distribution of vesicle pools in cerebellar parallel fibre terminals after depression of ectopic transmission
title_sort distribution of vesicle pools in cerebellar parallel fibre terminals after depression of ectopic transmission
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053221/
https://www.ncbi.nlm.nih.gov/pubmed/30024947
http://dx.doi.org/10.1371/journal.pone.0200937
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