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Spatiotemporal receptive fields of barrel cortex revealed by reverse correlation of synaptic input

Of all sensory areas, barrel cortex is among the best understood in terms of circuitry, yet least understood in terms of sensory function. We combined intracellular recording in rats with a novel multi-directional multi-whisker stimulator system to estimate receptive fields by reverse correlation of...

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Autores principales: Ramirez, Alejandro, Pnevmatikakis, Eftychios A., Merel, Josh, Paninski, Liam, Miller, Kenneth D., Bruno, Randy M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203687/
https://www.ncbi.nlm.nih.gov/pubmed/24836076
http://dx.doi.org/10.1038/nn.3720
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author Ramirez, Alejandro
Pnevmatikakis, Eftychios A.
Merel, Josh
Paninski, Liam
Miller, Kenneth D.
Bruno, Randy M.
author_facet Ramirez, Alejandro
Pnevmatikakis, Eftychios A.
Merel, Josh
Paninski, Liam
Miller, Kenneth D.
Bruno, Randy M.
author_sort Ramirez, Alejandro
collection PubMed
description Of all sensory areas, barrel cortex is among the best understood in terms of circuitry, yet least understood in terms of sensory function. We combined intracellular recording in rats with a novel multi-directional multi-whisker stimulator system to estimate receptive fields by reverse correlation of stimuli to synaptic inputs. Spatiotemporal receptive fields were identified orders of magnitude faster than by conventional spike-based approaches, even for neurons with little spiking activity. Given a suitable stimulus representation, a linear model captured the stimulus-response relationship for all neurons with surprisingly high accuracy. In contrast to conventional single-whisker stimuli, complex stimuli revealed dramatically sharpened receptive fields, largely due to adaptation. This phenomenon allowed the surround to facilitate rather than suppress responses to the principal whisker. Optimized stimuli enhanced firing in layers 4-6 but not 2/3, which remained sparsely active. Surround facilitation through adaptation may be required for discriminating complex shapes and textures during natural sensing.
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spelling pubmed-42036872014-12-01 Spatiotemporal receptive fields of barrel cortex revealed by reverse correlation of synaptic input Ramirez, Alejandro Pnevmatikakis, Eftychios A. Merel, Josh Paninski, Liam Miller, Kenneth D. Bruno, Randy M. Nat Neurosci Article Of all sensory areas, barrel cortex is among the best understood in terms of circuitry, yet least understood in terms of sensory function. We combined intracellular recording in rats with a novel multi-directional multi-whisker stimulator system to estimate receptive fields by reverse correlation of stimuli to synaptic inputs. Spatiotemporal receptive fields were identified orders of magnitude faster than by conventional spike-based approaches, even for neurons with little spiking activity. Given a suitable stimulus representation, a linear model captured the stimulus-response relationship for all neurons with surprisingly high accuracy. In contrast to conventional single-whisker stimuli, complex stimuli revealed dramatically sharpened receptive fields, largely due to adaptation. This phenomenon allowed the surround to facilitate rather than suppress responses to the principal whisker. Optimized stimuli enhanced firing in layers 4-6 but not 2/3, which remained sparsely active. Surround facilitation through adaptation may be required for discriminating complex shapes and textures during natural sensing. 2014-05-18 2014-06 /pmc/articles/PMC4203687/ /pubmed/24836076 http://dx.doi.org/10.1038/nn.3720 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
Ramirez, Alejandro
Pnevmatikakis, Eftychios A.
Merel, Josh
Paninski, Liam
Miller, Kenneth D.
Bruno, Randy M.
Spatiotemporal receptive fields of barrel cortex revealed by reverse correlation of synaptic input
title Spatiotemporal receptive fields of barrel cortex revealed by reverse correlation of synaptic input
title_full Spatiotemporal receptive fields of barrel cortex revealed by reverse correlation of synaptic input
title_fullStr Spatiotemporal receptive fields of barrel cortex revealed by reverse correlation of synaptic input
title_full_unstemmed Spatiotemporal receptive fields of barrel cortex revealed by reverse correlation of synaptic input
title_short Spatiotemporal receptive fields of barrel cortex revealed by reverse correlation of synaptic input
title_sort spatiotemporal receptive fields of barrel cortex revealed by reverse correlation of synaptic input
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203687/
https://www.ncbi.nlm.nih.gov/pubmed/24836076
http://dx.doi.org/10.1038/nn.3720
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