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Elimination of all redundant climbing fiber synapses requires granule cells in the postnatal cerebellum

Different afferent synapse populations interact to control the specificity of connections during neuronal circuit maturation. The elimination of all but one climbing-fiber onto each Purkinje cell during the development of the cerebellar cortex is a particularly well studied example of synaptic refin...

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Autores principales: Bailly, Yannick, Rabacchi, Sylvia, Sherrard, Rachel M., Rodeau, Jean-Luc, Demais, Valérie, Lohof, Ann M., Mariani, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030189/
https://www.ncbi.nlm.nih.gov/pubmed/29968809
http://dx.doi.org/10.1038/s41598-018-28398-7
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author Bailly, Yannick
Rabacchi, Sylvia
Sherrard, Rachel M.
Rodeau, Jean-Luc
Demais, Valérie
Lohof, Ann M.
Mariani, Jean
author_facet Bailly, Yannick
Rabacchi, Sylvia
Sherrard, Rachel M.
Rodeau, Jean-Luc
Demais, Valérie
Lohof, Ann M.
Mariani, Jean
author_sort Bailly, Yannick
collection PubMed
description Different afferent synapse populations interact to control the specificity of connections during neuronal circuit maturation. The elimination of all but one climbing-fiber onto each Purkinje cell during the development of the cerebellar cortex is a particularly well studied example of synaptic refinement. The suppression of granule cell precursors by X irradiation during postnatal days 4 to 7 prevents this synaptic refinement, indicating a critical role for granule cells. Several studies of cerebellar development have suggested that synapse elimination has a first phase which is granule cell-independent and a second phase which is granule cell-dependent. In this study, we show that sufficiently-strong irradiation restricted to postnatal days 5 or 6 completely abolishes climbing fiber synaptic refinement, leaving the olivo-cerebellar circuit in its immature configuration in the adult, with up to 5 climbing fibers innervating the Purkinje cell in some cases. This implies that the putative early phase of climbing fiber synapse elimination can be blocked by irradiation-induced granule cell loss if this loss is sufficiently large, and thus indicates that the entire process of climbing fiber synapse elimination requires the presence of an adequate number of granule cells. The specific critical period for this effect appears to be directly related to the timing of Purkinje cell and granule cell development in different cerebellar lobules, indicating a close, spatiotemporal synchrony between granule-cell development and olivo-cerebellar synaptic maturation.
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spelling pubmed-60301892018-07-11 Elimination of all redundant climbing fiber synapses requires granule cells in the postnatal cerebellum Bailly, Yannick Rabacchi, Sylvia Sherrard, Rachel M. Rodeau, Jean-Luc Demais, Valérie Lohof, Ann M. Mariani, Jean Sci Rep Article Different afferent synapse populations interact to control the specificity of connections during neuronal circuit maturation. The elimination of all but one climbing-fiber onto each Purkinje cell during the development of the cerebellar cortex is a particularly well studied example of synaptic refinement. The suppression of granule cell precursors by X irradiation during postnatal days 4 to 7 prevents this synaptic refinement, indicating a critical role for granule cells. Several studies of cerebellar development have suggested that synapse elimination has a first phase which is granule cell-independent and a second phase which is granule cell-dependent. In this study, we show that sufficiently-strong irradiation restricted to postnatal days 5 or 6 completely abolishes climbing fiber synaptic refinement, leaving the olivo-cerebellar circuit in its immature configuration in the adult, with up to 5 climbing fibers innervating the Purkinje cell in some cases. This implies that the putative early phase of climbing fiber synapse elimination can be blocked by irradiation-induced granule cell loss if this loss is sufficiently large, and thus indicates that the entire process of climbing fiber synapse elimination requires the presence of an adequate number of granule cells. The specific critical period for this effect appears to be directly related to the timing of Purkinje cell and granule cell development in different cerebellar lobules, indicating a close, spatiotemporal synchrony between granule-cell development and olivo-cerebellar synaptic maturation. Nature Publishing Group UK 2018-07-03 /pmc/articles/PMC6030189/ /pubmed/29968809 http://dx.doi.org/10.1038/s41598-018-28398-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bailly, Yannick
Rabacchi, Sylvia
Sherrard, Rachel M.
Rodeau, Jean-Luc
Demais, Valérie
Lohof, Ann M.
Mariani, Jean
Elimination of all redundant climbing fiber synapses requires granule cells in the postnatal cerebellum
title Elimination of all redundant climbing fiber synapses requires granule cells in the postnatal cerebellum
title_full Elimination of all redundant climbing fiber synapses requires granule cells in the postnatal cerebellum
title_fullStr Elimination of all redundant climbing fiber synapses requires granule cells in the postnatal cerebellum
title_full_unstemmed Elimination of all redundant climbing fiber synapses requires granule cells in the postnatal cerebellum
title_short Elimination of all redundant climbing fiber synapses requires granule cells in the postnatal cerebellum
title_sort elimination of all redundant climbing fiber synapses requires granule cells in the postnatal cerebellum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030189/
https://www.ncbi.nlm.nih.gov/pubmed/29968809
http://dx.doi.org/10.1038/s41598-018-28398-7
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