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Multimodal analysis demonstrating the shaping of functional gradients in the marmoset brain
The discovery of functional gradients introduce a new perspective in understanding the cortical spectrum of intrinsic dynamics, as it captures major axes of functional connectivity in low-dimensional space. However, how functional gradients arise and dynamically vary remains poorly understood. In th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633775/ https://www.ncbi.nlm.nih.gov/pubmed/36329036 http://dx.doi.org/10.1038/s41467-022-34371-w |
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author | Tong, Chuanjun Liu, Cirong Zhang, Kaiwei Bo, Binshi Xia, Ying Yang, Hao Feng, Yanqiu Liang, Zhifeng |
author_facet | Tong, Chuanjun Liu, Cirong Zhang, Kaiwei Bo, Binshi Xia, Ying Yang, Hao Feng, Yanqiu Liang, Zhifeng |
author_sort | Tong, Chuanjun |
collection | PubMed |
description | The discovery of functional gradients introduce a new perspective in understanding the cortical spectrum of intrinsic dynamics, as it captures major axes of functional connectivity in low-dimensional space. However, how functional gradients arise and dynamically vary remains poorly understood. In this study, we investigated the biological basis of functional gradients using awake resting-state fMRI, retrograde tracing and gene expression datasets in marmosets. We found functional gradients in marmosets showed a sensorimotor-to-visual principal gradient followed by a unimodal-to-multimodal gradient, resembling functional gradients in human children. Although strongly constrained by structural wirings, functional gradients were dynamically modulated by arousal levels. Utilizing a reduced model, we uncovered opposing effects on gradient dynamics by structural connectivity (inverted U-shape) and neuromodulatory input (U-shape) with arousal fluctuations, and dissected the contribution of individual neuromodulatory receptors. This study provides insights into biological basis of functional gradients by revealing the interaction between structural connectivity and ascending neuromodulatory system. |
format | Online Article Text |
id | pubmed-9633775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96337752022-11-05 Multimodal analysis demonstrating the shaping of functional gradients in the marmoset brain Tong, Chuanjun Liu, Cirong Zhang, Kaiwei Bo, Binshi Xia, Ying Yang, Hao Feng, Yanqiu Liang, Zhifeng Nat Commun Article The discovery of functional gradients introduce a new perspective in understanding the cortical spectrum of intrinsic dynamics, as it captures major axes of functional connectivity in low-dimensional space. However, how functional gradients arise and dynamically vary remains poorly understood. In this study, we investigated the biological basis of functional gradients using awake resting-state fMRI, retrograde tracing and gene expression datasets in marmosets. We found functional gradients in marmosets showed a sensorimotor-to-visual principal gradient followed by a unimodal-to-multimodal gradient, resembling functional gradients in human children. Although strongly constrained by structural wirings, functional gradients were dynamically modulated by arousal levels. Utilizing a reduced model, we uncovered opposing effects on gradient dynamics by structural connectivity (inverted U-shape) and neuromodulatory input (U-shape) with arousal fluctuations, and dissected the contribution of individual neuromodulatory receptors. This study provides insights into biological basis of functional gradients by revealing the interaction between structural connectivity and ascending neuromodulatory system. Nature Publishing Group UK 2022-11-03 /pmc/articles/PMC9633775/ /pubmed/36329036 http://dx.doi.org/10.1038/s41467-022-34371-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Tong, Chuanjun Liu, Cirong Zhang, Kaiwei Bo, Binshi Xia, Ying Yang, Hao Feng, Yanqiu Liang, Zhifeng Multimodal analysis demonstrating the shaping of functional gradients in the marmoset brain |
title | Multimodal analysis demonstrating the shaping of functional gradients in the marmoset brain |
title_full | Multimodal analysis demonstrating the shaping of functional gradients in the marmoset brain |
title_fullStr | Multimodal analysis demonstrating the shaping of functional gradients in the marmoset brain |
title_full_unstemmed | Multimodal analysis demonstrating the shaping of functional gradients in the marmoset brain |
title_short | Multimodal analysis demonstrating the shaping of functional gradients in the marmoset brain |
title_sort | multimodal analysis demonstrating the shaping of functional gradients in the marmoset brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633775/ https://www.ncbi.nlm.nih.gov/pubmed/36329036 http://dx.doi.org/10.1038/s41467-022-34371-w |
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