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Uncovering a tripartite landmark in posterior cingulate cortex
Understanding brain structure-function relationships, and their development and evolution, is central to neuroscience research. Here, we show that morphological differences in posterior cingulate cortex (PCC), a hub of functional brain networks, predict individual differences in macroanatomical, mic...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9451146/ https://www.ncbi.nlm.nih.gov/pubmed/36070384 http://dx.doi.org/10.1126/sciadv.abn9516 |
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author | Willbrand, Ethan H. Parker, Benjamin J. Voorhies, Willa I. Miller, Jacob A. Lyu, Ilwoo Hallock, Tyler Aponik-Gremillion, Lyndsey Koslov, Seth R. Bunge, Silvia A. Foster, Brett L. Weiner, Kevin S. |
author_facet | Willbrand, Ethan H. Parker, Benjamin J. Voorhies, Willa I. Miller, Jacob A. Lyu, Ilwoo Hallock, Tyler Aponik-Gremillion, Lyndsey Koslov, Seth R. Bunge, Silvia A. Foster, Brett L. Weiner, Kevin S. |
author_sort | Willbrand, Ethan H. |
collection | PubMed |
description | Understanding brain structure-function relationships, and their development and evolution, is central to neuroscience research. Here, we show that morphological differences in posterior cingulate cortex (PCC), a hub of functional brain networks, predict individual differences in macroanatomical, microstructural, and functional features of PCC. Manually labeling 4511 sulci in 572 hemispheres, we found a shallow cortical indentation (termed the inframarginal sulcus; ifrms) within PCC that is absent from neuroanatomical atlases yet colocalized with a focal, functional region of the lateral frontoparietal network implicated in cognitive control. This structural-functional coupling generalized to meta-analyses consisting of hundreds of studies and thousands of participants. Additional morphological analyses showed that unique properties of the ifrms differ across the life span and between hominoid species. These findings support a classic theory that shallow, tertiary sulci serve as landmarks in association cortices. They also beg the question: How many other cortical indentations have we missed? |
format | Online Article Text |
id | pubmed-9451146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-94511462022-09-29 Uncovering a tripartite landmark in posterior cingulate cortex Willbrand, Ethan H. Parker, Benjamin J. Voorhies, Willa I. Miller, Jacob A. Lyu, Ilwoo Hallock, Tyler Aponik-Gremillion, Lyndsey Koslov, Seth R. Bunge, Silvia A. Foster, Brett L. Weiner, Kevin S. Sci Adv Neuroscience Understanding brain structure-function relationships, and their development and evolution, is central to neuroscience research. Here, we show that morphological differences in posterior cingulate cortex (PCC), a hub of functional brain networks, predict individual differences in macroanatomical, microstructural, and functional features of PCC. Manually labeling 4511 sulci in 572 hemispheres, we found a shallow cortical indentation (termed the inframarginal sulcus; ifrms) within PCC that is absent from neuroanatomical atlases yet colocalized with a focal, functional region of the lateral frontoparietal network implicated in cognitive control. This structural-functional coupling generalized to meta-analyses consisting of hundreds of studies and thousands of participants. Additional morphological analyses showed that unique properties of the ifrms differ across the life span and between hominoid species. These findings support a classic theory that shallow, tertiary sulci serve as landmarks in association cortices. They also beg the question: How many other cortical indentations have we missed? American Association for the Advancement of Science 2022-09-07 /pmc/articles/PMC9451146/ /pubmed/36070384 http://dx.doi.org/10.1126/sciadv.abn9516 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Neuroscience Willbrand, Ethan H. Parker, Benjamin J. Voorhies, Willa I. Miller, Jacob A. Lyu, Ilwoo Hallock, Tyler Aponik-Gremillion, Lyndsey Koslov, Seth R. Bunge, Silvia A. Foster, Brett L. Weiner, Kevin S. Uncovering a tripartite landmark in posterior cingulate cortex |
title | Uncovering a tripartite landmark in posterior cingulate cortex |
title_full | Uncovering a tripartite landmark in posterior cingulate cortex |
title_fullStr | Uncovering a tripartite landmark in posterior cingulate cortex |
title_full_unstemmed | Uncovering a tripartite landmark in posterior cingulate cortex |
title_short | Uncovering a tripartite landmark in posterior cingulate cortex |
title_sort | uncovering a tripartite landmark in posterior cingulate cortex |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9451146/ https://www.ncbi.nlm.nih.gov/pubmed/36070384 http://dx.doi.org/10.1126/sciadv.abn9516 |
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