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Activity-dependent organization of prefrontal hub-networks for associative learning and signal transformation
Associative learning is crucial for adapting to environmental changes. Interactions among neuronal populations involving the dorso-medial prefrontal cortex (dmPFC) are proposed to regulate associative learning, but how these neuronal populations store and process information about the association re...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10558457/ https://www.ncbi.nlm.nih.gov/pubmed/37803014 http://dx.doi.org/10.1038/s41467-023-41547-5 |
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author | Agetsuma, Masakazu Sato, Issei Tanaka, Yasuhiro R. Carrillo-Reid, Luis Kasai, Atsushi Noritake, Atsushi Arai, Yoshiyuki Yoshitomo, Miki Inagaki, Takashi Yukawa, Hiroshi Hashimoto, Hitoshi Nabekura, Junichi Nagai, Takeharu |
author_facet | Agetsuma, Masakazu Sato, Issei Tanaka, Yasuhiro R. Carrillo-Reid, Luis Kasai, Atsushi Noritake, Atsushi Arai, Yoshiyuki Yoshitomo, Miki Inagaki, Takashi Yukawa, Hiroshi Hashimoto, Hitoshi Nabekura, Junichi Nagai, Takeharu |
author_sort | Agetsuma, Masakazu |
collection | PubMed |
description | Associative learning is crucial for adapting to environmental changes. Interactions among neuronal populations involving the dorso-medial prefrontal cortex (dmPFC) are proposed to regulate associative learning, but how these neuronal populations store and process information about the association remains unclear. Here we developed a pipeline for longitudinal two-photon imaging and computational dissection of neural population activities in male mouse dmPFC during fear-conditioning procedures, enabling us to detect learning-dependent changes in the dmPFC network topology. Using regularized regression methods and graphical modeling, we found that fear conditioning drove dmPFC reorganization to generate a neuronal ensemble encoding conditioned responses (CR) characterized by enhanced internal coactivity, functional connectivity, and association with conditioned stimuli (CS). Importantly, neurons strongly responding to unconditioned stimuli during conditioning subsequently became hubs of this novel associative network for the CS-to-CR transformation. Altogether, we demonstrate learning-dependent dynamic modulation of population coding structured on the activity-dependent formation of the hub network within the dmPFC. |
format | Online Article Text |
id | pubmed-10558457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105584572023-10-08 Activity-dependent organization of prefrontal hub-networks for associative learning and signal transformation Agetsuma, Masakazu Sato, Issei Tanaka, Yasuhiro R. Carrillo-Reid, Luis Kasai, Atsushi Noritake, Atsushi Arai, Yoshiyuki Yoshitomo, Miki Inagaki, Takashi Yukawa, Hiroshi Hashimoto, Hitoshi Nabekura, Junichi Nagai, Takeharu Nat Commun Article Associative learning is crucial for adapting to environmental changes. Interactions among neuronal populations involving the dorso-medial prefrontal cortex (dmPFC) are proposed to regulate associative learning, but how these neuronal populations store and process information about the association remains unclear. Here we developed a pipeline for longitudinal two-photon imaging and computational dissection of neural population activities in male mouse dmPFC during fear-conditioning procedures, enabling us to detect learning-dependent changes in the dmPFC network topology. Using regularized regression methods and graphical modeling, we found that fear conditioning drove dmPFC reorganization to generate a neuronal ensemble encoding conditioned responses (CR) characterized by enhanced internal coactivity, functional connectivity, and association with conditioned stimuli (CS). Importantly, neurons strongly responding to unconditioned stimuli during conditioning subsequently became hubs of this novel associative network for the CS-to-CR transformation. Altogether, we demonstrate learning-dependent dynamic modulation of population coding structured on the activity-dependent formation of the hub network within the dmPFC. Nature Publishing Group UK 2023-10-06 /pmc/articles/PMC10558457/ /pubmed/37803014 http://dx.doi.org/10.1038/s41467-023-41547-5 Text en © The Author(s) 2023 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Agetsuma, Masakazu Sato, Issei Tanaka, Yasuhiro R. Carrillo-Reid, Luis Kasai, Atsushi Noritake, Atsushi Arai, Yoshiyuki Yoshitomo, Miki Inagaki, Takashi Yukawa, Hiroshi Hashimoto, Hitoshi Nabekura, Junichi Nagai, Takeharu Activity-dependent organization of prefrontal hub-networks for associative learning and signal transformation |
title | Activity-dependent organization of prefrontal hub-networks for associative learning and signal transformation |
title_full | Activity-dependent organization of prefrontal hub-networks for associative learning and signal transformation |
title_fullStr | Activity-dependent organization of prefrontal hub-networks for associative learning and signal transformation |
title_full_unstemmed | Activity-dependent organization of prefrontal hub-networks for associative learning and signal transformation |
title_short | Activity-dependent organization of prefrontal hub-networks for associative learning and signal transformation |
title_sort | activity-dependent organization of prefrontal hub-networks for associative learning and signal transformation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10558457/ https://www.ncbi.nlm.nih.gov/pubmed/37803014 http://dx.doi.org/10.1038/s41467-023-41547-5 |
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