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Cell assemblies at multiple time scales with arbitrary lag constellations

Hebb's idea of a cell assembly as the fundamental unit of neural information processing has dominated neuroscience like no other theoretical concept within the past 60 years. A range of different physiological phenomena, from precisely synchronized spiking to broadly simultaneous rate increases...

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Detalles Bibliográficos
Autores principales: Russo, Eleonora, Durstewitz, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226654/
https://www.ncbi.nlm.nih.gov/pubmed/28074777
http://dx.doi.org/10.7554/eLife.19428
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author Russo, Eleonora
Durstewitz, Daniel
author_facet Russo, Eleonora
Durstewitz, Daniel
author_sort Russo, Eleonora
collection PubMed
description Hebb's idea of a cell assembly as the fundamental unit of neural information processing has dominated neuroscience like no other theoretical concept within the past 60 years. A range of different physiological phenomena, from precisely synchronized spiking to broadly simultaneous rate increases, has been subsumed under this term. Yet progress in this area is hampered by the lack of statistical tools that would enable to extract assemblies with arbitrary constellations of time lags, and at multiple temporal scales, partly due to the severe computational burden. Here we present such a unifying methodological and conceptual framework which detects assembly structure at many different time scales, levels of precision, and with arbitrary internal organization. Applying this methodology to multiple single unit recordings from various cortical areas, we find that there is no universal cortical coding scheme, but that assembly structure and precision significantly depends on the brain area recorded and ongoing task demands. DOI: http://dx.doi.org/10.7554/eLife.19428.001
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spelling pubmed-52266542017-01-13 Cell assemblies at multiple time scales with arbitrary lag constellations Russo, Eleonora Durstewitz, Daniel eLife Computational and Systems Biology Hebb's idea of a cell assembly as the fundamental unit of neural information processing has dominated neuroscience like no other theoretical concept within the past 60 years. A range of different physiological phenomena, from precisely synchronized spiking to broadly simultaneous rate increases, has been subsumed under this term. Yet progress in this area is hampered by the lack of statistical tools that would enable to extract assemblies with arbitrary constellations of time lags, and at multiple temporal scales, partly due to the severe computational burden. Here we present such a unifying methodological and conceptual framework which detects assembly structure at many different time scales, levels of precision, and with arbitrary internal organization. Applying this methodology to multiple single unit recordings from various cortical areas, we find that there is no universal cortical coding scheme, but that assembly structure and precision significantly depends on the brain area recorded and ongoing task demands. DOI: http://dx.doi.org/10.7554/eLife.19428.001 eLife Sciences Publications, Ltd 2017-01-11 /pmc/articles/PMC5226654/ /pubmed/28074777 http://dx.doi.org/10.7554/eLife.19428 Text en © 2017, Russo et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Russo, Eleonora
Durstewitz, Daniel
Cell assemblies at multiple time scales with arbitrary lag constellations
title Cell assemblies at multiple time scales with arbitrary lag constellations
title_full Cell assemblies at multiple time scales with arbitrary lag constellations
title_fullStr Cell assemblies at multiple time scales with arbitrary lag constellations
title_full_unstemmed Cell assemblies at multiple time scales with arbitrary lag constellations
title_short Cell assemblies at multiple time scales with arbitrary lag constellations
title_sort cell assemblies at multiple time scales with arbitrary lag constellations
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226654/
https://www.ncbi.nlm.nih.gov/pubmed/28074777
http://dx.doi.org/10.7554/eLife.19428
work_keys_str_mv AT russoeleonora cellassembliesatmultipletimescaleswitharbitrarylagconstellations
AT durstewitzdaniel cellassembliesatmultipletimescaleswitharbitrarylagconstellations