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Macaque Area V2/V3 Reorganization Following Homonymous Retinal Lesions

In the adult visual system, topographic reorganization of the primary visual cortex (V1) after retinal lesions has been extensively investigated. In contrast, the plasticity of higher order extrastriate areas following retinal lesions is less well studied. Here, we used fMRI to study reorganization...

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Autores principales: Keliris, Georgios A., Shao, Yibin, Schmid, Michael C., Augath, Mark, Logothetis, Nikos K., Smirnakis, Stelios M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832035/
https://www.ncbi.nlm.nih.gov/pubmed/35153666
http://dx.doi.org/10.3389/fnins.2022.757091
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author Keliris, Georgios A.
Shao, Yibin
Schmid, Michael C.
Augath, Mark
Logothetis, Nikos K.
Smirnakis, Stelios M.
author_facet Keliris, Georgios A.
Shao, Yibin
Schmid, Michael C.
Augath, Mark
Logothetis, Nikos K.
Smirnakis, Stelios M.
author_sort Keliris, Georgios A.
collection PubMed
description In the adult visual system, topographic reorganization of the primary visual cortex (V1) after retinal lesions has been extensively investigated. In contrast, the plasticity of higher order extrastriate areas following retinal lesions is less well studied. Here, we used fMRI to study reorganization of visual areas V2/V3 following the induction of permanent, binocular, homonymous retinal lesions in 4 adult macaque monkeys. We found that the great majority of voxels that did not show visual modulation on the day of the lesion in the V2/V3 lesion projection zone (LPZ) demonstrated significant visual modulations 2 weeks later, and the mean modulation strength remained approximately stable thereafter for the duration of our observations (4–5 months). The distribution of eccentricities of visually modulated voxels inside the V2/V3 LPZ spanned a wider range post-lesion than pre-lesion, suggesting that neurons inside the LPZ reorganize by receiving input either from the foveal or the peripheral border of the LPZ, depending on proximity. Overall, we conclude that area V2/V3 of adult rhesus macaques displays a significant capacity for topographic reorganization following retinal lesions markedly exceeding the corresponding capacity of area V1.
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spelling pubmed-88320352022-02-12 Macaque Area V2/V3 Reorganization Following Homonymous Retinal Lesions Keliris, Georgios A. Shao, Yibin Schmid, Michael C. Augath, Mark Logothetis, Nikos K. Smirnakis, Stelios M. Front Neurosci Neuroscience In the adult visual system, topographic reorganization of the primary visual cortex (V1) after retinal lesions has been extensively investigated. In contrast, the plasticity of higher order extrastriate areas following retinal lesions is less well studied. Here, we used fMRI to study reorganization of visual areas V2/V3 following the induction of permanent, binocular, homonymous retinal lesions in 4 adult macaque monkeys. We found that the great majority of voxels that did not show visual modulation on the day of the lesion in the V2/V3 lesion projection zone (LPZ) demonstrated significant visual modulations 2 weeks later, and the mean modulation strength remained approximately stable thereafter for the duration of our observations (4–5 months). The distribution of eccentricities of visually modulated voxels inside the V2/V3 LPZ spanned a wider range post-lesion than pre-lesion, suggesting that neurons inside the LPZ reorganize by receiving input either from the foveal or the peripheral border of the LPZ, depending on proximity. Overall, we conclude that area V2/V3 of adult rhesus macaques displays a significant capacity for topographic reorganization following retinal lesions markedly exceeding the corresponding capacity of area V1. Frontiers Media S.A. 2022-01-28 /pmc/articles/PMC8832035/ /pubmed/35153666 http://dx.doi.org/10.3389/fnins.2022.757091 Text en Copyright © 2022 Keliris, Shao, Schmid, Augath, Logothetis and Smirnakis. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Keliris, Georgios A.
Shao, Yibin
Schmid, Michael C.
Augath, Mark
Logothetis, Nikos K.
Smirnakis, Stelios M.
Macaque Area V2/V3 Reorganization Following Homonymous Retinal Lesions
title Macaque Area V2/V3 Reorganization Following Homonymous Retinal Lesions
title_full Macaque Area V2/V3 Reorganization Following Homonymous Retinal Lesions
title_fullStr Macaque Area V2/V3 Reorganization Following Homonymous Retinal Lesions
title_full_unstemmed Macaque Area V2/V3 Reorganization Following Homonymous Retinal Lesions
title_short Macaque Area V2/V3 Reorganization Following Homonymous Retinal Lesions
title_sort macaque area v2/v3 reorganization following homonymous retinal lesions
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832035/
https://www.ncbi.nlm.nih.gov/pubmed/35153666
http://dx.doi.org/10.3389/fnins.2022.757091
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