An Emergent Population Code in Primary Auditory Cortex Supports Selective Attention to Spectral and Temporal Sound Features.


Journal

The Journal of neuroscience : the official journal of the Society for Neuroscience
ISSN: 1529-2401
Titre abrégé: J Neurosci
Pays: United States
ID NLM: 8102140

Informations de publication

Date de publication:
08 09 2021
Historique:
received: 25 03 2020
revised: 19 05 2021
accepted: 28 05 2021
pubmed: 3 7 2021
medline: 27 11 2021
entrez: 2 7 2021
Statut: ppublish

Résumé

Textbook descriptions of primary sensory cortex (PSC) revolve around single neurons' representation of low-dimensional sensory features, such as visual object orientation in primary visual cortex (V1), location of somatic touch in primary somatosensory cortex (S1), and sound frequency in primary auditory cortex (A1). Typically, studies of PSC measure neurons' responses along few (one or two) stimulus and/or behavioral dimensions. However, real-world stimuli usually vary along many feature dimensions and behavioral demands change constantly. In order to illuminate how A1 supports flexible perception in rich acoustic environments, we recorded from A1 neurons while rhesus macaques (one male, one female) performed a feature-selective attention task. We presented sounds that varied along spectral and temporal feature dimensions (carrier bandwidth and temporal envelope, respectively). Within a block, subjects attended to one feature of the sound in a selective change detection task. We found that single neurons tend to be high-dimensional, in that they exhibit substantial mixed selectivity for both sound features, as well as task context. We found no overall enhancement of single-neuron coding of the attended feature, as attention could either diminish or enhance this coding. However, a population-level analysis reveals that ensembles of neurons exhibit enhanced encoding of attended sound features, and this population code tracks subjects' performance. Importantly, surrogate neural populations with intact single-neuron tuning but shuffled higher-order correlations among neurons fail to yield attention- related effects observed in the intact data. These results suggest that an emergent population code not measurable at the single-neuron level might constitute the functional unit of sensory representation in PSC.

Identifiants

pubmed: 34210783
pii: JNEUROSCI.0693-20.2021
doi: 10.1523/JNEUROSCI.0693-20.2021
pmc: PMC8425978
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

7561-7577

Subventions

Organisme : NIDCD NIH HHS
ID : R01 DC002514
Pays : United States

Informations de copyright

Copyright © 2021 the authors.

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Auteurs

Joshua D Downer (JD)

Center for Neuroscience, University of California, Davis, Davis, California 95618 joshua.downer@ucsf.edu mlsutter@ucdavis.edu.
Department of Otolaryngology, Head and Neck Surgery, University of California, San Francisco, California 94143.

Jessica R Verhein (JR)

Center for Neuroscience, University of California, Davis, Davis, California 95618.
School of Medicine, Stanford University, Stanford, California 94305.

Brittany C Rapone (BC)

Center for Neuroscience, University of California, Davis, Davis, California 95618.
School of Social Sciences, Oxford Brookes University, Oxford, OX4 0BP, United Kingdom.

Kevin N O'Connor (KN)

Center for Neuroscience, University of California, Davis, Davis, California 95618.
Department of Neurobiology, Physiology and Behavior, University of California, Davis, Davis, California 95618.

Mitchell L Sutter (ML)

Center for Neuroscience, University of California, Davis, Davis, California 95618 joshua.downer@ucsf.edu mlsutter@ucdavis.edu.
Department of Neurobiology, Physiology and Behavior, University of California, Davis, Davis, California 95618.

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