Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1784611846297223168 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8654357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT robertblaise afunctionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes AT kimchieyaly afunctionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes AT watanabeyurika afunctionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes AT chakomatatenda afunctionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes AT jingmiao afunctionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes AT liyulong afunctionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes AT polleydanielb afunctionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes AT robertblaise functionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes AT kimchieyaly functionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes AT watanabeyurika functionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes AT chakomatatenda functionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes AT jingmiao functionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes AT liyulong functionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes AT polleydanielb functionaltopographywithinthecholinergicbasalforebrainforencodingsensorycuesandbehavioralreinforcementoutcomes |