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Fine-Grained Topography and Modularity of the Macaque Frontal Pole Cortex Revealed by Anatomical Connectivity Profiles

The frontal pole cortex (FPC) plays key roles in various higher-order functions and is highly developed in non-human primates. An essential missing piece of information is the detailed anatomical connections for finer parcellation of the macaque FPC than provided by the previous tracer results. This...

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Autores principales: He, Bin, Cao, Long, Xia, Xiaoluan, Zhang, Baogui, Zhang, Dan, You, Bo, Fan, Lingzhong, Jiang, Tianzi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719154/
https://www.ncbi.nlm.nih.gov/pubmed/33108588
http://dx.doi.org/10.1007/s12264-020-00589-1
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author He, Bin
Cao, Long
Xia, Xiaoluan
Zhang, Baogui
Zhang, Dan
You, Bo
Fan, Lingzhong
Jiang, Tianzi
author_facet He, Bin
Cao, Long
Xia, Xiaoluan
Zhang, Baogui
Zhang, Dan
You, Bo
Fan, Lingzhong
Jiang, Tianzi
author_sort He, Bin
collection PubMed
description The frontal pole cortex (FPC) plays key roles in various higher-order functions and is highly developed in non-human primates. An essential missing piece of information is the detailed anatomical connections for finer parcellation of the macaque FPC than provided by the previous tracer results. This is important for understanding the functional architecture of the cerebral cortex. Here, combining cross-validation and principal component analysis, we formed a tractography-based parcellation scheme that applied a machine learning algorithm to divide the macaque FPC (2 males and 6 females) into eight subareas using high-resolution diffusion magnetic resonance imaging with the 9.4T Bruker system, and then revealed their subregional connections. Furthermore, we applied improved hierarchical clustering to the obtained parcels to probe the modular structure of the subregions, and found that the dorsolateral FPC, which contains an extension to the medial FPC, was mainly connected to regions of the default-mode network. The ventral FPC was mainly involved in the social-interaction network and the dorsal FPC in the metacognitive network. These results enhance our understanding of the anatomy and circuitry of the macaque brain, and contribute to FPC-related clinical research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12264-020-00589-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-77191542020-12-07 Fine-Grained Topography and Modularity of the Macaque Frontal Pole Cortex Revealed by Anatomical Connectivity Profiles He, Bin Cao, Long Xia, Xiaoluan Zhang, Baogui Zhang, Dan You, Bo Fan, Lingzhong Jiang, Tianzi Neurosci Bull Original Article The frontal pole cortex (FPC) plays key roles in various higher-order functions and is highly developed in non-human primates. An essential missing piece of information is the detailed anatomical connections for finer parcellation of the macaque FPC than provided by the previous tracer results. This is important for understanding the functional architecture of the cerebral cortex. Here, combining cross-validation and principal component analysis, we formed a tractography-based parcellation scheme that applied a machine learning algorithm to divide the macaque FPC (2 males and 6 females) into eight subareas using high-resolution diffusion magnetic resonance imaging with the 9.4T Bruker system, and then revealed their subregional connections. Furthermore, we applied improved hierarchical clustering to the obtained parcels to probe the modular structure of the subregions, and found that the dorsolateral FPC, which contains an extension to the medial FPC, was mainly connected to regions of the default-mode network. The ventral FPC was mainly involved in the social-interaction network and the dorsal FPC in the metacognitive network. These results enhance our understanding of the anatomy and circuitry of the macaque brain, and contribute to FPC-related clinical research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12264-020-00589-1) contains supplementary material, which is available to authorized users. Springer Singapore 2020-10-27 /pmc/articles/PMC7719154/ /pubmed/33108588 http://dx.doi.org/10.1007/s12264-020-00589-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
He, Bin
Cao, Long
Xia, Xiaoluan
Zhang, Baogui
Zhang, Dan
You, Bo
Fan, Lingzhong
Jiang, Tianzi
Fine-Grained Topography and Modularity of the Macaque Frontal Pole Cortex Revealed by Anatomical Connectivity Profiles
title Fine-Grained Topography and Modularity of the Macaque Frontal Pole Cortex Revealed by Anatomical Connectivity Profiles
title_full Fine-Grained Topography and Modularity of the Macaque Frontal Pole Cortex Revealed by Anatomical Connectivity Profiles
title_fullStr Fine-Grained Topography and Modularity of the Macaque Frontal Pole Cortex Revealed by Anatomical Connectivity Profiles
title_full_unstemmed Fine-Grained Topography and Modularity of the Macaque Frontal Pole Cortex Revealed by Anatomical Connectivity Profiles
title_short Fine-Grained Topography and Modularity of the Macaque Frontal Pole Cortex Revealed by Anatomical Connectivity Profiles
title_sort fine-grained topography and modularity of the macaque frontal pole cortex revealed by anatomical connectivity profiles
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719154/
https://www.ncbi.nlm.nih.gov/pubmed/33108588
http://dx.doi.org/10.1007/s12264-020-00589-1
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