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The Cytoarchitecture of Domain-specific Regions in Human High-level Visual Cortex

A fundamental hypothesis in neuroscience proposes that underlying cellular architecture (cytoarchitecture) contributes to the functionality of a brain area. However, this hypothesis has not been tested in human ventral temporal cortex (VTC) that contains domain-specific regions causally involved in...

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Autores principales: Weiner, Kevin S., Barnett, Michael A., Lorenz, Simon, Caspers, Julian, Stigliani, Anthony, Amunts, Katrin, Zilles, Karl, Fischl, Bruce, Grill-Spector, Kalanit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5939223/
https://www.ncbi.nlm.nih.gov/pubmed/27909003
http://dx.doi.org/10.1093/cercor/bhw361
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author Weiner, Kevin S.
Barnett, Michael A.
Lorenz, Simon
Caspers, Julian
Stigliani, Anthony
Amunts, Katrin
Zilles, Karl
Fischl, Bruce
Grill-Spector, Kalanit
author_facet Weiner, Kevin S.
Barnett, Michael A.
Lorenz, Simon
Caspers, Julian
Stigliani, Anthony
Amunts, Katrin
Zilles, Karl
Fischl, Bruce
Grill-Spector, Kalanit
author_sort Weiner, Kevin S.
collection PubMed
description A fundamental hypothesis in neuroscience proposes that underlying cellular architecture (cytoarchitecture) contributes to the functionality of a brain area. However, this hypothesis has not been tested in human ventral temporal cortex (VTC) that contains domain-specific regions causally involved in perception. To fill this gap in knowledge, we used cortex-based alignment to register functional regions from living participants to cytoarchitectonic areas in ex vivo brains. This novel approach reveals 3 findings. First, there is a consistent relationship between domain-specific regions and cytoarchitectonic areas: each functional region is largely restricted to 1 cytoarchitectonic area. Second, extracting cytoarchitectonic profiles from face- and place-selective regions after back-projecting each region to 20-μm thick histological sections indicates that cytoarchitectonic properties distinguish these regions from each other. Third, some cytoarchitectonic areas contain more than 1 domain-specific region. For example, face-, body-, and character-selective regions are located within the same cytoarchitectonic area. We summarize these findings with a parsimonious hypothesis incorporating how cellular properties may contribute to functional specialization in human VTC. Specifically, we link computational principles to correlated axes of functional and cytoarchitectonic segregation in human VTC, in which parallel processing across domains occurs along a lateral–medial axis while transformations of information within domain occur along an anterior–posterior axis.
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spelling pubmed-59392232018-05-10 The Cytoarchitecture of Domain-specific Regions in Human High-level Visual Cortex Weiner, Kevin S. Barnett, Michael A. Lorenz, Simon Caspers, Julian Stigliani, Anthony Amunts, Katrin Zilles, Karl Fischl, Bruce Grill-Spector, Kalanit Cereb Cortex Original Articles A fundamental hypothesis in neuroscience proposes that underlying cellular architecture (cytoarchitecture) contributes to the functionality of a brain area. However, this hypothesis has not been tested in human ventral temporal cortex (VTC) that contains domain-specific regions causally involved in perception. To fill this gap in knowledge, we used cortex-based alignment to register functional regions from living participants to cytoarchitectonic areas in ex vivo brains. This novel approach reveals 3 findings. First, there is a consistent relationship between domain-specific regions and cytoarchitectonic areas: each functional region is largely restricted to 1 cytoarchitectonic area. Second, extracting cytoarchitectonic profiles from face- and place-selective regions after back-projecting each region to 20-μm thick histological sections indicates that cytoarchitectonic properties distinguish these regions from each other. Third, some cytoarchitectonic areas contain more than 1 domain-specific region. For example, face-, body-, and character-selective regions are located within the same cytoarchitectonic area. We summarize these findings with a parsimonious hypothesis incorporating how cellular properties may contribute to functional specialization in human VTC. Specifically, we link computational principles to correlated axes of functional and cytoarchitectonic segregation in human VTC, in which parallel processing across domains occurs along a lateral–medial axis while transformations of information within domain occur along an anterior–posterior axis. Oxford University Press 2017-01 2016-12-01 /pmc/articles/PMC5939223/ /pubmed/27909003 http://dx.doi.org/10.1093/cercor/bhw361 Text en © The Author 2016. Published by Oxford University Press. 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
Weiner, Kevin S.
Barnett, Michael A.
Lorenz, Simon
Caspers, Julian
Stigliani, Anthony
Amunts, Katrin
Zilles, Karl
Fischl, Bruce
Grill-Spector, Kalanit
The Cytoarchitecture of Domain-specific Regions in Human High-level Visual Cortex
title The Cytoarchitecture of Domain-specific Regions in Human High-level Visual Cortex
title_full The Cytoarchitecture of Domain-specific Regions in Human High-level Visual Cortex
title_fullStr The Cytoarchitecture of Domain-specific Regions in Human High-level Visual Cortex
title_full_unstemmed The Cytoarchitecture of Domain-specific Regions in Human High-level Visual Cortex
title_short The Cytoarchitecture of Domain-specific Regions in Human High-level Visual Cortex
title_sort cytoarchitecture of domain-specific regions in human high-level visual cortex
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5939223/
https://www.ncbi.nlm.nih.gov/pubmed/27909003
http://dx.doi.org/10.1093/cercor/bhw361
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