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Functional connectivity of visual cortex in the blind follows retinotopic organization principles
Is visual input during critical periods of development crucial for the emergence of the fundamental topographical mapping of the visual cortex? And would this structure be retained throughout life-long blindness or would it fade as a result of plastic, use-based reorganization? We used functional co...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614142/ https://www.ncbi.nlm.nih.gov/pubmed/25869851 http://dx.doi.org/10.1093/brain/awv083 |
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author | Striem-Amit, Ella Ovadia-Caro, Smadar Caramazza, Alfonso Margulies, Daniel S. Villringer, Arno Amedi, Amir |
author_facet | Striem-Amit, Ella Ovadia-Caro, Smadar Caramazza, Alfonso Margulies, Daniel S. Villringer, Arno Amedi, Amir |
author_sort | Striem-Amit, Ella |
collection | PubMed |
description | Is visual input during critical periods of development crucial for the emergence of the fundamental topographical mapping of the visual cortex? And would this structure be retained throughout life-long blindness or would it fade as a result of plastic, use-based reorganization? We used functional connectivity magnetic resonance imaging based on intrinsic blood oxygen level-dependent fluctuations to investigate whether significant traces of topographical mapping of the visual scene in the form of retinotopic organization, could be found in congenitally blind adults. A group of 11 fully and congenitally blind subjects and 18 sighted controls were studied. The blind demonstrated an intact functional connectivity network structural organization of the three main retinotopic mapping axes: eccentricity (centre-periphery), laterality (left-right), and elevation (upper-lower) throughout the retinotopic cortex extending to high-level ventral and dorsal streams, including characteristic eccentricity biases in face- and house-selective areas. Functional connectivity-based topographic organization in the visual cortex was indistinguishable from the normally sighted retinotopic functional connectivity structure as indicated by clustering analysis, and was found even in participants who did not have a typical retinal development in utero (microphthalmics). While the internal structural organization of the visual cortex was strikingly similar, the blind exhibited profound differences in functional connectivity to other (non-visual) brain regions as compared to the sighted, which were specific to portions of V1. Central V1 was more connected to language areas but peripheral V1 to spatial attention and control networks. These findings suggest that current accounts of critical periods and experience-dependent development should be revisited even for primary sensory areas, in that the connectivity basis for visual cortex large-scale topographical organization can develop without any visual experience and be retained through life-long experience-dependent plasticity. Furthermore, retinotopic divisions of labour, such as that between the visual cortex regions normally representing the fovea and periphery, also form the basis for topographically-unique plastic changes in the blind. |
format | Online Article Text |
id | pubmed-4614142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-46141422015-10-26 Functional connectivity of visual cortex in the blind follows retinotopic organization principles Striem-Amit, Ella Ovadia-Caro, Smadar Caramazza, Alfonso Margulies, Daniel S. Villringer, Arno Amedi, Amir Brain Original Articles Is visual input during critical periods of development crucial for the emergence of the fundamental topographical mapping of the visual cortex? And would this structure be retained throughout life-long blindness or would it fade as a result of plastic, use-based reorganization? We used functional connectivity magnetic resonance imaging based on intrinsic blood oxygen level-dependent fluctuations to investigate whether significant traces of topographical mapping of the visual scene in the form of retinotopic organization, could be found in congenitally blind adults. A group of 11 fully and congenitally blind subjects and 18 sighted controls were studied. The blind demonstrated an intact functional connectivity network structural organization of the three main retinotopic mapping axes: eccentricity (centre-periphery), laterality (left-right), and elevation (upper-lower) throughout the retinotopic cortex extending to high-level ventral and dorsal streams, including characteristic eccentricity biases in face- and house-selective areas. Functional connectivity-based topographic organization in the visual cortex was indistinguishable from the normally sighted retinotopic functional connectivity structure as indicated by clustering analysis, and was found even in participants who did not have a typical retinal development in utero (microphthalmics). While the internal structural organization of the visual cortex was strikingly similar, the blind exhibited profound differences in functional connectivity to other (non-visual) brain regions as compared to the sighted, which were specific to portions of V1. Central V1 was more connected to language areas but peripheral V1 to spatial attention and control networks. These findings suggest that current accounts of critical periods and experience-dependent development should be revisited even for primary sensory areas, in that the connectivity basis for visual cortex large-scale topographical organization can develop without any visual experience and be retained through life-long experience-dependent plasticity. Furthermore, retinotopic divisions of labour, such as that between the visual cortex regions normally representing the fovea and periphery, also form the basis for topographically-unique plastic changes in the blind. Oxford University Press 2015-06 2015-04-10 /pmc/articles/PMC4614142/ /pubmed/25869851 http://dx.doi.org/10.1093/brain/awv083 Text en © The Author (2015). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Articles Striem-Amit, Ella Ovadia-Caro, Smadar Caramazza, Alfonso Margulies, Daniel S. Villringer, Arno Amedi, Amir Functional connectivity of visual cortex in the blind follows retinotopic organization principles |
title | Functional connectivity of visual cortex in the blind follows retinotopic organization principles |
title_full | Functional connectivity of visual cortex in the blind follows retinotopic organization principles |
title_fullStr | Functional connectivity of visual cortex in the blind follows retinotopic organization principles |
title_full_unstemmed | Functional connectivity of visual cortex in the blind follows retinotopic organization principles |
title_short | Functional connectivity of visual cortex in the blind follows retinotopic organization principles |
title_sort | functional connectivity of visual cortex in the blind follows retinotopic organization principles |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614142/ https://www.ncbi.nlm.nih.gov/pubmed/25869851 http://dx.doi.org/10.1093/brain/awv083 |
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