Attentional modulation of neuronal variability in circuit models of cortex
The circuit mechanisms behind shared neural variability (noise correlation) and its dependence on neural state are poorly understood. Visual attention is well-suited to constrain cortical models of response variability because attention both increases firing rates and their stimulus sensitivity, as...
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doaj-671dbfca9db642328c755f526e99a6662021-05-05T13:31:41ZengeLife Sciences Publications LtdeLife2050-084X2017-06-01610.7554/eLife.23978Attentional modulation of neuronal variability in circuit models of cortexTatjana Kanashiro0Gabriel Koch Ocker1Marlene R Cohen2https://orcid.org/0000-0001-8583-4300Brent Doiron3https://orcid.org/0000-0002-6916-5511Program for Neural Computation, Carnegie Mellon University and University of Pittsburgh, Pittsburgh, United States; Department of Mathematics, University of Pittsburgh, Pittsburgh, United States; Center for the Neural Basis of Cognition, Pittsburgh, United StatesDepartment of Mathematics, University of Pittsburgh, Pittsburgh, United States; Center for the Neural Basis of Cognition, Pittsburgh, United States; Allen Institute for Brain Science, Seattle, United StatesCenter for the Neural Basis of Cognition, Pittsburgh, United States; Department of Neuroscience, University of Pittsburgh, Pittsburgh, United StatesDepartment of Mathematics, University of Pittsburgh, Pittsburgh, United States; Center for the Neural Basis of Cognition, Pittsburgh, United StatesThe circuit mechanisms behind shared neural variability (noise correlation) and its dependence on neural state are poorly understood. Visual attention is well-suited to constrain cortical models of response variability because attention both increases firing rates and their stimulus sensitivity, as well as decreases noise correlations. We provide a novel analysis of population recordings in rhesus primate visual area V4 showing that a single biophysical mechanism may underlie these diverse neural correlates of attention. We explore model cortical networks where top-down mediated increases in excitability, distributed across excitatory and inhibitory targets, capture the key neuronal correlates of attention. Our models predict that top-down signals primarily affect inhibitory neurons, whereas excitatory neurons are more sensitive to stimulus specific bottom-up inputs. Accounting for trial variability in models of state dependent modulation of neuronal activity is a critical step in building a mechanistic theory of neuronal cognition.https://elifesciences.org/articles/23978noise correlationsinhibitory feedbackneural correlates of attentionmean field model |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tatjana Kanashiro Gabriel Koch Ocker Marlene R Cohen Brent Doiron |
spellingShingle |
Tatjana Kanashiro Gabriel Koch Ocker Marlene R Cohen Brent Doiron Attentional modulation of neuronal variability in circuit models of cortex eLife noise correlations inhibitory feedback neural correlates of attention mean field model |
author_facet |
Tatjana Kanashiro Gabriel Koch Ocker Marlene R Cohen Brent Doiron |
author_sort |
Tatjana Kanashiro |
title |
Attentional modulation of neuronal variability in circuit models of cortex |
title_short |
Attentional modulation of neuronal variability in circuit models of cortex |
title_full |
Attentional modulation of neuronal variability in circuit models of cortex |
title_fullStr |
Attentional modulation of neuronal variability in circuit models of cortex |
title_full_unstemmed |
Attentional modulation of neuronal variability in circuit models of cortex |
title_sort |
attentional modulation of neuronal variability in circuit models of cortex |
publisher |
eLife Sciences Publications Ltd |
series |
eLife |
issn |
2050-084X |
publishDate |
2017-06-01 |
description |
The circuit mechanisms behind shared neural variability (noise correlation) and its dependence on neural state are poorly understood. Visual attention is well-suited to constrain cortical models of response variability because attention both increases firing rates and their stimulus sensitivity, as well as decreases noise correlations. We provide a novel analysis of population recordings in rhesus primate visual area V4 showing that a single biophysical mechanism may underlie these diverse neural correlates of attention. We explore model cortical networks where top-down mediated increases in excitability, distributed across excitatory and inhibitory targets, capture the key neuronal correlates of attention. Our models predict that top-down signals primarily affect inhibitory neurons, whereas excitatory neurons are more sensitive to stimulus specific bottom-up inputs. Accounting for trial variability in models of state dependent modulation of neuronal activity is a critical step in building a mechanistic theory of neuronal cognition. |
topic |
noise correlations inhibitory feedback neural correlates of attention mean field model |
url |
https://elifesciences.org/articles/23978 |
work_keys_str_mv |
AT tatjanakanashiro attentionalmodulationofneuronalvariabilityincircuitmodelsofcortex AT gabrielkochocker attentionalmodulationofneuronalvariabilityincircuitmodelsofcortex AT marlenercohen attentionalmodulationofneuronalvariabilityincircuitmodelsofcortex AT brentdoiron attentionalmodulationofneuronalvariabilityincircuitmodelsofcortex |
_version_ |
1721461643169234944 |