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Synapse elimination in the developing cerebellum

Neural circuits in neonatal animals contain numerous redundant synapses that are functionally immature. During the postnatal period, unnecessary synapses are eliminated while functionally important synapses become stronger and mature. The climbing fiber (CF) to the Purkinje cell (PC) synapse is a re...

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Detalles Bibliográficos
Autores principales: Hashimoto, Kouichi, Kano, Masanobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Basel 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830199/
https://www.ncbi.nlm.nih.gov/pubmed/23811844
http://dx.doi.org/10.1007/s00018-013-1405-2
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author Hashimoto, Kouichi
Kano, Masanobu
author_facet Hashimoto, Kouichi
Kano, Masanobu
author_sort Hashimoto, Kouichi
collection PubMed
description Neural circuits in neonatal animals contain numerous redundant synapses that are functionally immature. During the postnatal period, unnecessary synapses are eliminated while functionally important synapses become stronger and mature. The climbing fiber (CF) to the Purkinje cell (PC) synapse is a representative model for the analysis of postnatal refinement of neuronal circuits in the central nervous system. PCs are initially innervated by multiple CFs with similar strengths around postnatal day 3 (P3). Only a single CF is selectively strengthened during P3–P7 (functional differentiation), and the strengthened CF undergoes translocation from soma to dendrites of PCs from P9 on (dendritic translocation). Following the functional differentiation, supernumerary CF synapses on the soma are eliminated, which proceeds in two distinct phases: the early phase from P7 to around P11 and the late phase from around P12 to P17. Here, we review our current understanding of cellular and molecular mechanisms of CF synapse elimination in the developing cerebellum.
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spelling pubmed-38301992013-11-26 Synapse elimination in the developing cerebellum Hashimoto, Kouichi Kano, Masanobu Cell Mol Life Sci Review Neural circuits in neonatal animals contain numerous redundant synapses that are functionally immature. During the postnatal period, unnecessary synapses are eliminated while functionally important synapses become stronger and mature. The climbing fiber (CF) to the Purkinje cell (PC) synapse is a representative model for the analysis of postnatal refinement of neuronal circuits in the central nervous system. PCs are initially innervated by multiple CFs with similar strengths around postnatal day 3 (P3). Only a single CF is selectively strengthened during P3–P7 (functional differentiation), and the strengthened CF undergoes translocation from soma to dendrites of PCs from P9 on (dendritic translocation). Following the functional differentiation, supernumerary CF synapses on the soma are eliminated, which proceeds in two distinct phases: the early phase from P7 to around P11 and the late phase from around P12 to P17. Here, we review our current understanding of cellular and molecular mechanisms of CF synapse elimination in the developing cerebellum. Springer Basel 2013-06-28 2013 /pmc/articles/PMC3830199/ /pubmed/23811844 http://dx.doi.org/10.1007/s00018-013-1405-2 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Review
Hashimoto, Kouichi
Kano, Masanobu
Synapse elimination in the developing cerebellum
title Synapse elimination in the developing cerebellum
title_full Synapse elimination in the developing cerebellum
title_fullStr Synapse elimination in the developing cerebellum
title_full_unstemmed Synapse elimination in the developing cerebellum
title_short Synapse elimination in the developing cerebellum
title_sort synapse elimination in the developing cerebellum
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830199/
https://www.ncbi.nlm.nih.gov/pubmed/23811844
http://dx.doi.org/10.1007/s00018-013-1405-2
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