Cellular-resolution optogenetics reveals attenuation-by-suppression in visual cortical neurons.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
05 Nov 2024
Historique:
medline: 1 11 2024
pubmed: 1 11 2024
entrez: 1 11 2024
Statut: ppublish

Résumé

The relationship between neurons' input and spiking output is central to brain computation. Studies in vitro and in anesthetized animals suggest that nonlinearities emerge in cells' input-output (IO; activation) functions as network activity increases, yet how neurons transform inputs in vivo has been unclear. Here, we characterize cortical principal neurons' activation functions in awake mice using two-photon optogenetics. We deliver fixed inputs at the soma while neurons' activity varies with sensory stimuli. We find that responses to fixed optogenetic input are nearly unchanged as neurons are excited, reflecting a linear response regime above neurons' resting point. In contrast, responses are dramatically attenuated by suppression. This attenuation is a powerful means to filter inputs arriving to suppressed cells, privileging other inputs arriving to excited neurons. These results have two major implications. First, somatic neural activation functions in vivo accord with the activation functions used in recent machine learning systems. Second, neurons' IO functions can filter sensory inputs-not only do sensory stimuli change neurons' spiking outputs, but these changes also affect responses to input, attenuating responses to some inputs while leaving others unchanged.

Identifiants

pubmed: 39485801
doi: 10.1073/pnas.2318837121
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2318837121

Subventions

Organisme : HHS | NIH (NIH)
ID : U19NS107464
Organisme : HHS | NIH (NIH)
ID : ZIAMH0020967

Déclaration de conflit d'intérêts

Competing interests statement:The authors declare no competing interest.

Auteurs

Paul K LaFosse (PK)

Intramural Program, National Institute of Mental Health, NIH, Bethesda, MD 20892.
NIH-University of Maryland Graduate Partnerships Program, NIH, Bethesda, MD 20892.
Neuroscience and Cognitive Science Program, University of Maryland College Park, College Park, MD 20742.

Zhishang Zhou (Z)

Intramural Program, National Institute of Mental Health, NIH, Bethesda, MD 20892.

Jonathan F O'Rawe (JF)

Intramural Program, National Institute of Mental Health, NIH, Bethesda, MD 20892.

Nina G Friedman (NG)

Intramural Program, National Institute of Mental Health, NIH, Bethesda, MD 20892.
NIH-University of Maryland Graduate Partnerships Program, NIH, Bethesda, MD 20892.
Neuroscience and Cognitive Science Program, University of Maryland College Park, College Park, MD 20742.

Victoria M Scott (VM)

Intramural Program, National Institute of Mental Health, NIH, Bethesda, MD 20892.

Yanting Deng (Y)

Intramural Program, National Institute of Mental Health, NIH, Bethesda, MD 20892.

Mark H Histed (MH)

Intramural Program, National Institute of Mental Health, NIH, Bethesda, MD 20892.

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