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The Regulation of Corticofugal Fiber Targeting by Retinal Inputs

Corticothalamic projection systems arise from 2 main cortical layers. Layer V neurons project exclusively to higher-order thalamic nuclei, while layer VIa fibers project to both first-order and higher-order thalamic nuclei. During early postnatal development, layer VIa and VIb fibers accumulate at t...

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Autores principales: Grant, Eleanor, Hoerder-Suabedissen, Anna, Molnár, Zoltán
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737616/
https://www.ncbi.nlm.nih.gov/pubmed/26744542
http://dx.doi.org/10.1093/cercor/bhv315
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author Grant, Eleanor
Hoerder-Suabedissen, Anna
Molnár, Zoltán
author_facet Grant, Eleanor
Hoerder-Suabedissen, Anna
Molnár, Zoltán
author_sort Grant, Eleanor
collection PubMed
description Corticothalamic projection systems arise from 2 main cortical layers. Layer V neurons project exclusively to higher-order thalamic nuclei, while layer VIa fibers project to both first-order and higher-order thalamic nuclei. During early postnatal development, layer VIa and VIb fibers accumulate at the borders of the dorsal lateral geniculate nucleus (dLGN) before they innervate it. After neonatal monocular enucleation or silencing of the early retinal activity, there is premature entry of layer VIa and VIb fibers into the dLGN contralateral to the manipulation. Layer V fibers do not innervate the superficial gray layer of the superior colliculus during the first postnatal week, but also demonstrate premature entry to the contralateral superficial gray layer following neonatal enucleation. Normally, layer V driver projections to the thalamus only innervate higher-order nuclei. Our results demonstrate that removal of retinal input from the dLGN induces cortical layer V projections to aberrantly enter, arborize, and synapse within the first-order dLGN. These results suggest that there is cross-hierarchical corticothalamic plasticity after monocular enucleation. Cross-hierarchical rewiring has been previously demonstrated in the thalamocortical system (Pouchelon et al. 2014), and now we provide evidence for cross-hierarchical corticothalamic rewiring after loss of the peripheral sensory input.
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spelling pubmed-47376162016-02-03 The Regulation of Corticofugal Fiber Targeting by Retinal Inputs Grant, Eleanor Hoerder-Suabedissen, Anna Molnár, Zoltán Cereb Cortex Original Articles Corticothalamic projection systems arise from 2 main cortical layers. Layer V neurons project exclusively to higher-order thalamic nuclei, while layer VIa fibers project to both first-order and higher-order thalamic nuclei. During early postnatal development, layer VIa and VIb fibers accumulate at the borders of the dorsal lateral geniculate nucleus (dLGN) before they innervate it. After neonatal monocular enucleation or silencing of the early retinal activity, there is premature entry of layer VIa and VIb fibers into the dLGN contralateral to the manipulation. Layer V fibers do not innervate the superficial gray layer of the superior colliculus during the first postnatal week, but also demonstrate premature entry to the contralateral superficial gray layer following neonatal enucleation. Normally, layer V driver projections to the thalamus only innervate higher-order nuclei. Our results demonstrate that removal of retinal input from the dLGN induces cortical layer V projections to aberrantly enter, arborize, and synapse within the first-order dLGN. These results suggest that there is cross-hierarchical corticothalamic plasticity after monocular enucleation. Cross-hierarchical rewiring has been previously demonstrated in the thalamocortical system (Pouchelon et al. 2014), and now we provide evidence for cross-hierarchical corticothalamic rewiring after loss of the peripheral sensory input. Oxford University Press 2016-03 2016-01-06 /pmc/articles/PMC4737616/ /pubmed/26744542 http://dx.doi.org/10.1093/cercor/bhv315 Text en © The Author 2016. Published by Oxford University Press 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Grant, Eleanor
Hoerder-Suabedissen, Anna
Molnár, Zoltán
The Regulation of Corticofugal Fiber Targeting by Retinal Inputs
title The Regulation of Corticofugal Fiber Targeting by Retinal Inputs
title_full The Regulation of Corticofugal Fiber Targeting by Retinal Inputs
title_fullStr The Regulation of Corticofugal Fiber Targeting by Retinal Inputs
title_full_unstemmed The Regulation of Corticofugal Fiber Targeting by Retinal Inputs
title_short The Regulation of Corticofugal Fiber Targeting by Retinal Inputs
title_sort regulation of corticofugal fiber targeting by retinal inputs
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737616/
https://www.ncbi.nlm.nih.gov/pubmed/26744542
http://dx.doi.org/10.1093/cercor/bhv315
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