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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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.
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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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