Transformation of valence signaling in a mouse striatopallidal circuit.


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
30 Oct 2024
Historique:
medline: 30 10 2024
pubmed: 30 10 2024
entrez: 30 10 2024
Statut: epublish

Résumé

The ways in which sensory stimuli acquire motivational valence through association with other stimuli is one of the simplest forms of learning. Although we have identified many brain nuclei that play various roles in reward processing, a significant gap remains in understanding how valence encoding transforms through the layers of sensory processing. To address this gap, we carried out a comparative investigation of the mouse anteromedial olfactory tubercle (OT), and the ventral pallidum (VP) - 2 connected nuclei of the basal ganglia which have both been implicated in reward processing. First, using anterograde and retrograde tracing, we show that both D1 and D2 neurons of the anteromedial OT project primarily to the VP and minimally elsewhere. Using two-photon calcium imaging, we then investigated how the identity of the odor and reward contingency of the odor are differently encoded by neurons in either structure during a classical conditioning paradigm. We find that VP neurons robustly encode reward contingency, but not identity, in low-dimensional space. In contrast, the OT neurons primarily encode odor identity in high-dimensional space. Although D1 OT neurons showed larger responses to rewarded odors than other odors, consistent with prior findings, we interpret this as identity encoding with enhanced contrast. Finally, using a novel conditioning paradigm that decouples reward contingency and licking vigor, we show that both features are encoded by non-overlapping VP neurons. These results provide a novel framework for the striatopallidal circuit in which a high-dimensional encoding of stimulus identity is collapsed onto a low-dimensional encoding of motivational valence.

Identifiants

pubmed: 39475384
doi: 10.7554/eLife.90976
pii: 90976
doi:
pii:

Banques de données

Dryad
['10.5061/dryad.2547d7x15']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIDCD NIH HHS
ID : R01DC018313
Pays : United States
Organisme : NIDCD NIH HHS
ID : R00DC014516
Pays : United States

Informations de copyright

© 2023, Lee et al.

Déclaration de conflit d'intérêts

DL, NL, LL, CR No competing interests declared

Auteurs

Donghyung Lee (D)

University of California San Diego, Department of Neurobiology, School of Biological Sciences, San Diego, United States.

Nathan Lau (N)

University of California San Diego, Department of Neurobiology, School of Biological Sciences, San Diego, United States.

Lillian Liu (L)

University of California San Diego, Department of Neurobiology, School of Biological Sciences, San Diego, United States.

Cory M Root (CM)

University of California San Diego, Department of Neurobiology, School of Biological Sciences, San Diego, United States.

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Classifications MeSH