A Distinct Class of Bursting Neurons with Strong Gamma Synchronization and Stimulus Selectivity in Monkey V1.


Journal

Neuron
ISSN: 1097-4199
Titre abrégé: Neuron
Pays: United States
ID NLM: 8809320

Informations de publication

Date de publication:
08 01 2020
Historique:
received: 01 04 2019
revised: 12 07 2019
accepted: 23 09 2019
pubmed: 17 11 2019
medline: 31 3 2020
entrez: 17 11 2019
Statut: ppublish

Résumé

Cortical computation depends on interactions between excitatory and inhibitory neurons. The contributions of distinct neuron types to sensory processing and network synchronization in primate visual cortex remain largely undetermined. We show that in awake monkey V1, there exists a distinct cell type (››30% of neurons) that has narrow-waveform (NW) action potentials and high spontaneous discharge rates and fires in high-frequency bursts. These neurons are more stimulus selective and phase locked to 30- to 80-Hz gamma oscillations than other neuron types. Unlike other neuron types, their gamma-phase locking is highly predictive of orientation tuning. We find evidence for strong rhythmic inhibition in these neurons, suggesting that they interact with interneurons to act as excitatory pacemakers for the V1 gamma rhythm. We did not find a similar class of NW bursting neurons in L2-L4 of mouse V1. Given its properties, this class of NW bursting neurons should be pivotal for the encoding and transmission of stimulus information.

Identifiants

pubmed: 31732258
pii: S0896-6273(19)30842-6
doi: 10.1016/j.neuron.2019.09.039
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

180-197.e5

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Irene Onorato (I)

Ernst Strüngmann Institute (ESI) for Neuroscience in Cooperation with Max Planck Society, Frankfurt, Germany; International Max Planck Research School for Neural Circuits, Frankfurt am Main, Germany.

Sergio Neuenschwander (S)

Max Planck Institute for Brain Research, Frankfurt, Germany; Brain Institute, Federal University of Rio Grande do Norte, Natal, Brazil.

Jennifer Hoy (J)

Institute of Neuroscience and Department of Biology, University of Oregon, Eugene, OR, USA.

Bruss Lima (B)

Max Planck Institute for Brain Research, Frankfurt, Germany.

Katia-Simone Rocha (KS)

Brain Institute, Federal University of Rio Grande do Norte, Natal, Brazil.

Ana Clara Broggini (AC)

Ernst Strüngmann Institute (ESI) for Neuroscience in Cooperation with Max Planck Society, Frankfurt, Germany.

Cem Uran (C)

Ernst Strüngmann Institute (ESI) for Neuroscience in Cooperation with Max Planck Society, Frankfurt, Germany.

Georgios Spyropoulos (G)

Ernst Strüngmann Institute (ESI) for Neuroscience in Cooperation with Max Planck Society, Frankfurt, Germany; International Max Planck Research School for Neural Circuits, Frankfurt am Main, Germany.

Johanna Klon-Lipok (J)

Ernst Strüngmann Institute (ESI) for Neuroscience in Cooperation with Max Planck Society, Frankfurt, Germany; Max Planck Institute for Brain Research, Frankfurt, Germany.

Thilo Womelsdorf (T)

Vanderbilt University, Nashville, TN, USA.

Pascal Fries (P)

Ernst Strüngmann Institute (ESI) for Neuroscience in Cooperation with Max Planck Society, Frankfurt, Germany.

Cristopher Niell (C)

Institute of Neuroscience and Department of Biology, University of Oregon, Eugene, OR, USA.

Wolf Singer (W)

Ernst Strüngmann Institute (ESI) for Neuroscience in Cooperation with Max Planck Society, Frankfurt, Germany; Max Planck Institute for Brain Research, Frankfurt, Germany; Frankfurt Institute for Advanced Studies, Frankfurt, Germany.

Martin Vinck (M)

Ernst Strüngmann Institute (ESI) for Neuroscience in Cooperation with Max Planck Society, Frankfurt, Germany. Electronic address: martin.vinck@esi-frankfurt.de.

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