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Structural plasticity of climbing fibers and the growth-associated protein GAP-43

Structural plasticity occurs physiologically or after brain damage to adapt or re-establish proper synaptic connections. This capacity depends on several intrinsic and extrinsic determinants that differ between neuron types. We reviewed the significant endogenous regenerative potential of the neuron...

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Detalles Bibliográficos
Autores principales: Grasselli, Giorgio, Strata, Piergiorgio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3578352/
https://www.ncbi.nlm.nih.gov/pubmed/23441024
http://dx.doi.org/10.3389/fncir.2013.00025
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author Grasselli, Giorgio
Strata, Piergiorgio
author_facet Grasselli, Giorgio
Strata, Piergiorgio
author_sort Grasselli, Giorgio
collection PubMed
description Structural plasticity occurs physiologically or after brain damage to adapt or re-establish proper synaptic connections. This capacity depends on several intrinsic and extrinsic determinants that differ between neuron types. We reviewed the significant endogenous regenerative potential of the neurons of the inferior olive (IO) in the adult rodent brain and the structural remodeling of the terminal arbor of their axons, the climbing fiber (CF), under various experimental conditions, focusing on the growth-associated protein GAP-43. CFs undergo remarkable collateral sprouting in the presence of denervated Purkinje cells (PCs) that are available for new innervation. In addition, severed olivo-cerebellar axons regenerate across the white matter through a graft of embryonic Schwann cells. In contrast, CFs undergo a regressive modification when their target is deleted. In vivo knockdown of GAP-43 in olivary neurons, leads to the atrophy of their CFs and a reduction in the ability to sprout toward surrounding denervated PCs. These findings demonstrate that GAP-43 is essential for promoting denervation-induced sprouting and maintaining normal CF architecture.
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spelling pubmed-35783522013-02-22 Structural plasticity of climbing fibers and the growth-associated protein GAP-43 Grasselli, Giorgio Strata, Piergiorgio Front Neural Circuits Neuroscience Structural plasticity occurs physiologically or after brain damage to adapt or re-establish proper synaptic connections. This capacity depends on several intrinsic and extrinsic determinants that differ between neuron types. We reviewed the significant endogenous regenerative potential of the neurons of the inferior olive (IO) in the adult rodent brain and the structural remodeling of the terminal arbor of their axons, the climbing fiber (CF), under various experimental conditions, focusing on the growth-associated protein GAP-43. CFs undergo remarkable collateral sprouting in the presence of denervated Purkinje cells (PCs) that are available for new innervation. In addition, severed olivo-cerebellar axons regenerate across the white matter through a graft of embryonic Schwann cells. In contrast, CFs undergo a regressive modification when their target is deleted. In vivo knockdown of GAP-43 in olivary neurons, leads to the atrophy of their CFs and a reduction in the ability to sprout toward surrounding denervated PCs. These findings demonstrate that GAP-43 is essential for promoting denervation-induced sprouting and maintaining normal CF architecture. Frontiers Media S.A. 2013-02-21 /pmc/articles/PMC3578352/ /pubmed/23441024 http://dx.doi.org/10.3389/fncir.2013.00025 Text en Copyright © 2013 Grasselli and Strata. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Grasselli, Giorgio
Strata, Piergiorgio
Structural plasticity of climbing fibers and the growth-associated protein GAP-43
title Structural plasticity of climbing fibers and the growth-associated protein GAP-43
title_full Structural plasticity of climbing fibers and the growth-associated protein GAP-43
title_fullStr Structural plasticity of climbing fibers and the growth-associated protein GAP-43
title_full_unstemmed Structural plasticity of climbing fibers and the growth-associated protein GAP-43
title_short Structural plasticity of climbing fibers and the growth-associated protein GAP-43
title_sort structural plasticity of climbing fibers and the growth-associated protein gap-43
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3578352/
https://www.ncbi.nlm.nih.gov/pubmed/23441024
http://dx.doi.org/10.3389/fncir.2013.00025
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