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Origins of choice-related activity in mouse somatosensory cortex

During perceptual decisions about faint or ambiguous sensory stimuli, even identical stimuli can produce different choices. Spike trains from sensory cortex neurons can predict trial-to-trial variability in choice. Choice-related spiking is widely studied to link cortical activity to perception, but...

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Detalles Bibliográficos
Autores principales: Yang, Hongdian, Kwon, Sung E., Severson, Kyle S., O’Connor, Daniel H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696889/
https://www.ncbi.nlm.nih.gov/pubmed/26642088
http://dx.doi.org/10.1038/nn.4183
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author Yang, Hongdian
Kwon, Sung E.
Severson, Kyle S.
O’Connor, Daniel H.
author_facet Yang, Hongdian
Kwon, Sung E.
Severson, Kyle S.
O’Connor, Daniel H.
author_sort Yang, Hongdian
collection PubMed
description During perceptual decisions about faint or ambiguous sensory stimuli, even identical stimuli can produce different choices. Spike trains from sensory cortex neurons can predict trial-to-trial variability in choice. Choice-related spiking is widely studied to link cortical activity to perception, but its origins remain unclear. Using imaging and electrophysiology, we found that mouse primary somatosensory cortex neurons showed robust choice-related activity during a tactile detection task. Spike trains from primary mechanoreceptive neurons did not predict choices about identical stimuli. Spike trains from thalamic relay neurons showed highly transient, weak choice-related activity. Intracellular recordings in cortex revealed a prolonged choice-related depolarization in most neurons that was not accounted for by feedforward thalamic input. Top-down axons projecting from secondary to primary somatosensory cortex signaled choice. An intracellular measure of stimulus sensitivity determined which neurons converted choice-related depolarization into spiking. Our results reveal how choice-related spiking emerges across neural circuits and within single neurons.
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spelling pubmed-46968892016-06-07 Origins of choice-related activity in mouse somatosensory cortex Yang, Hongdian Kwon, Sung E. Severson, Kyle S. O’Connor, Daniel H. Nat Neurosci Article During perceptual decisions about faint or ambiguous sensory stimuli, even identical stimuli can produce different choices. Spike trains from sensory cortex neurons can predict trial-to-trial variability in choice. Choice-related spiking is widely studied to link cortical activity to perception, but its origins remain unclear. Using imaging and electrophysiology, we found that mouse primary somatosensory cortex neurons showed robust choice-related activity during a tactile detection task. Spike trains from primary mechanoreceptive neurons did not predict choices about identical stimuli. Spike trains from thalamic relay neurons showed highly transient, weak choice-related activity. Intracellular recordings in cortex revealed a prolonged choice-related depolarization in most neurons that was not accounted for by feedforward thalamic input. Top-down axons projecting from secondary to primary somatosensory cortex signaled choice. An intracellular measure of stimulus sensitivity determined which neurons converted choice-related depolarization into spiking. Our results reveal how choice-related spiking emerges across neural circuits and within single neurons. 2015-12-07 2016-01 /pmc/articles/PMC4696889/ /pubmed/26642088 http://dx.doi.org/10.1038/nn.4183 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Yang, Hongdian
Kwon, Sung E.
Severson, Kyle S.
O’Connor, Daniel H.
Origins of choice-related activity in mouse somatosensory cortex
title Origins of choice-related activity in mouse somatosensory cortex
title_full Origins of choice-related activity in mouse somatosensory cortex
title_fullStr Origins of choice-related activity in mouse somatosensory cortex
title_full_unstemmed Origins of choice-related activity in mouse somatosensory cortex
title_short Origins of choice-related activity in mouse somatosensory cortex
title_sort origins of choice-related activity in mouse somatosensory cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696889/
https://www.ncbi.nlm.nih.gov/pubmed/26642088
http://dx.doi.org/10.1038/nn.4183
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