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Short-term plasticity at cerebellar granule cell to molecular layer interneuron synapses expands information processing
Information processing by cerebellar molecular layer interneurons (MLIs) plays a crucial role in motor behavior. MLI recruitment is tightly controlled by the profile of short-term plasticity (STP) at granule cell (GC)-MLI synapses. While GCs are the most numerous neurons in the brain, STP diversity...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533085/ https://www.ncbi.nlm.nih.gov/pubmed/31081751 http://dx.doi.org/10.7554/eLife.41586 |
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author | Dorgans, Kevin Demais, Valérie Bailly, Yannick Poulain, Bernard Isope, Philippe Doussau, Frédéric |
author_facet | Dorgans, Kevin Demais, Valérie Bailly, Yannick Poulain, Bernard Isope, Philippe Doussau, Frédéric |
author_sort | Dorgans, Kevin |
collection | PubMed |
description | Information processing by cerebellar molecular layer interneurons (MLIs) plays a crucial role in motor behavior. MLI recruitment is tightly controlled by the profile of short-term plasticity (STP) at granule cell (GC)-MLI synapses. While GCs are the most numerous neurons in the brain, STP diversity at GC-MLI synapses is poorly documented. Here, we studied how single MLIs are recruited by their distinct GC inputs during burst firing. Using slice recordings at individual GC-MLI synapses of mice, we revealed four classes of connections segregated by their STP profile. Each class differentially drives MLI recruitment. We show that GC synaptic diversity is underlain by heterogeneous expression of synapsin II, a key actor of STP and that GC terminals devoid of synapsin II are associated with slow MLI recruitment. Our study reveals that molecular, structural and functional diversity across GC terminals provides a mechanism to expand the coding range of MLIs. |
format | Online Article Text |
id | pubmed-6533085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-65330852019-05-28 Short-term plasticity at cerebellar granule cell to molecular layer interneuron synapses expands information processing Dorgans, Kevin Demais, Valérie Bailly, Yannick Poulain, Bernard Isope, Philippe Doussau, Frédéric eLife Neuroscience Information processing by cerebellar molecular layer interneurons (MLIs) plays a crucial role in motor behavior. MLI recruitment is tightly controlled by the profile of short-term plasticity (STP) at granule cell (GC)-MLI synapses. While GCs are the most numerous neurons in the brain, STP diversity at GC-MLI synapses is poorly documented. Here, we studied how single MLIs are recruited by their distinct GC inputs during burst firing. Using slice recordings at individual GC-MLI synapses of mice, we revealed four classes of connections segregated by their STP profile. Each class differentially drives MLI recruitment. We show that GC synaptic diversity is underlain by heterogeneous expression of synapsin II, a key actor of STP and that GC terminals devoid of synapsin II are associated with slow MLI recruitment. Our study reveals that molecular, structural and functional diversity across GC terminals provides a mechanism to expand the coding range of MLIs. eLife Sciences Publications, Ltd 2019-05-13 /pmc/articles/PMC6533085/ /pubmed/31081751 http://dx.doi.org/10.7554/eLife.41586 Text en © 2019, Dorgans et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Dorgans, Kevin Demais, Valérie Bailly, Yannick Poulain, Bernard Isope, Philippe Doussau, Frédéric Short-term plasticity at cerebellar granule cell to molecular layer interneuron synapses expands information processing |
title | Short-term plasticity at cerebellar granule cell to molecular layer interneuron synapses expands information processing |
title_full | Short-term plasticity at cerebellar granule cell to molecular layer interneuron synapses expands information processing |
title_fullStr | Short-term plasticity at cerebellar granule cell to molecular layer interneuron synapses expands information processing |
title_full_unstemmed | Short-term plasticity at cerebellar granule cell to molecular layer interneuron synapses expands information processing |
title_short | Short-term plasticity at cerebellar granule cell to molecular layer interneuron synapses expands information processing |
title_sort | short-term plasticity at cerebellar granule cell to molecular layer interneuron synapses expands information processing |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533085/ https://www.ncbi.nlm.nih.gov/pubmed/31081751 http://dx.doi.org/10.7554/eLife.41586 |
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