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A functional topography within the cholinergic basal forebrain for encoding sensory cues and behavioral reinforcement outcomes

Basal forebrain cholinergic neurons (BFCNs) project throughout the cortex to regulate arousal, stimulus salience, plasticity, and learning. Although often treated as a monolithic structure, the basal forebrain features distinct connectivity along its rostrocaudal axis that could impart regional diff...

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Autores principales: Robert, Blaise, Kimchi, Eyal Y, Watanabe, Yurika, Chakoma, Tatenda, Jing, Miao, Li, Yulong, Polley, Daniel B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654357/
https://www.ncbi.nlm.nih.gov/pubmed/34821218
http://dx.doi.org/10.7554/eLife.69514
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author Robert, Blaise
Kimchi, Eyal Y
Watanabe, Yurika
Chakoma, Tatenda
Jing, Miao
Li, Yulong
Polley, Daniel B
author_facet Robert, Blaise
Kimchi, Eyal Y
Watanabe, Yurika
Chakoma, Tatenda
Jing, Miao
Li, Yulong
Polley, Daniel B
author_sort Robert, Blaise
collection PubMed
description Basal forebrain cholinergic neurons (BFCNs) project throughout the cortex to regulate arousal, stimulus salience, plasticity, and learning. Although often treated as a monolithic structure, the basal forebrain features distinct connectivity along its rostrocaudal axis that could impart regional differences in BFCN processing. Here, we performed simultaneous bulk calcium imaging from rostral and caudal BFCNs over a 1-month period of variable reinforcement learning in mice. BFCNs in both regions showed equivalently weak responses to unconditioned visual stimuli and anticipated rewards. Rostral BFCNs in the horizontal limb of the diagonal band were more responsive to reward omission, more accurately classified behavioral outcomes, and more closely tracked fluctuations in pupil-indexed global brain state. Caudal tail BFCNs in globus pallidus and substantia innominata were more responsive to unconditioned auditory stimuli, orofacial movements, aversive reinforcement, and showed robust associative plasticity for punishment-predicting cues. These results identify a functional topography that diversifies cholinergic modulatory signals broadcast to downstream brain regions.
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spelling pubmed-86543572021-12-09 A functional topography within the cholinergic basal forebrain for encoding sensory cues and behavioral reinforcement outcomes Robert, Blaise Kimchi, Eyal Y Watanabe, Yurika Chakoma, Tatenda Jing, Miao Li, Yulong Polley, Daniel B eLife Neuroscience Basal forebrain cholinergic neurons (BFCNs) project throughout the cortex to regulate arousal, stimulus salience, plasticity, and learning. Although often treated as a monolithic structure, the basal forebrain features distinct connectivity along its rostrocaudal axis that could impart regional differences in BFCN processing. Here, we performed simultaneous bulk calcium imaging from rostral and caudal BFCNs over a 1-month period of variable reinforcement learning in mice. BFCNs in both regions showed equivalently weak responses to unconditioned visual stimuli and anticipated rewards. Rostral BFCNs in the horizontal limb of the diagonal band were more responsive to reward omission, more accurately classified behavioral outcomes, and more closely tracked fluctuations in pupil-indexed global brain state. Caudal tail BFCNs in globus pallidus and substantia innominata were more responsive to unconditioned auditory stimuli, orofacial movements, aversive reinforcement, and showed robust associative plasticity for punishment-predicting cues. These results identify a functional topography that diversifies cholinergic modulatory signals broadcast to downstream brain regions. eLife Sciences Publications, Ltd 2021-11-25 /pmc/articles/PMC8654357/ /pubmed/34821218 http://dx.doi.org/10.7554/eLife.69514 Text en © 2021, Robert et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Robert, Blaise
Kimchi, Eyal Y
Watanabe, Yurika
Chakoma, Tatenda
Jing, Miao
Li, Yulong
Polley, Daniel B
A functional topography within the cholinergic basal forebrain for encoding sensory cues and behavioral reinforcement outcomes
title A functional topography within the cholinergic basal forebrain for encoding sensory cues and behavioral reinforcement outcomes
title_full A functional topography within the cholinergic basal forebrain for encoding sensory cues and behavioral reinforcement outcomes
title_fullStr A functional topography within the cholinergic basal forebrain for encoding sensory cues and behavioral reinforcement outcomes
title_full_unstemmed A functional topography within the cholinergic basal forebrain for encoding sensory cues and behavioral reinforcement outcomes
title_short A functional topography within the cholinergic basal forebrain for encoding sensory cues and behavioral reinforcement outcomes
title_sort functional topography within the cholinergic basal forebrain for encoding sensory cues and behavioral reinforcement outcomes
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654357/
https://www.ncbi.nlm.nih.gov/pubmed/34821218
http://dx.doi.org/10.7554/eLife.69514
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