Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0105324
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dc.titleLarge-scale, high-resolution multielectrode-array recording depicts functional network differences of cortical and hippocampal cultures
dc.contributor.authorIto S.
dc.contributor.authorYeh F.-C.
dc.contributor.authorHiolski E.
dc.contributor.authorRydygier P.
dc.contributor.authorGunning D.E.
dc.contributor.authorHottowy P.
dc.contributor.authorTimme N.
dc.contributor.authorLitke A.M.
dc.contributor.authorBeggs J.M.
dc.date.accessioned2019-11-05T00:33:27Z
dc.date.available2019-11-05T00:33:27Z
dc.date.issued2014
dc.identifier.citationIto S., Yeh F.-C., Hiolski E., Rydygier P., Gunning D.E., Hottowy P., Timme N., Litke A.M., Beggs J.M. (2014). Large-scale, high-resolution multielectrode-array recording depicts functional network differences of cortical and hippocampal cultures. PLoS ONE 9 (8) : e105324. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0105324
dc.identifier.issn1932-6203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161387
dc.description.abstractUnderstanding the detailed circuitry of functioning neuronal networks is one of the major goals of neuroscience. Recent improvements in neuronal recording techniques have made it possible to record the spiking activity from hundreds of neurons simultaneously with sub-millisecond temporal resolution. Here we used a 512-channel multielectrode array system to record the activity from hundreds of neurons in organotypic cultures of cortico-hippocampal brain slices from mice. To probe the network structure, we employed a wavelet transform of the cross-correlogram to categorize the functional connectivity in different frequency ranges. With this method we directly compare, for the first time, in any preparation, the neuronal network structures of cortex and hippocampus, on the scale of hundreds of neurons, with sub-millisecond time resolution. Among the three frequency ranges that we investigated, the lower two frequency ranges (gamma (30-80 Hz) and beta (12-30 Hz) range) showed similar network structure between cortex and hippocampus, but there were many significant differences between these structures in the high frequency range (100-1000 Hz). The high frequency networks in cortex showed short tailed degree-distributions, shorter decay length of connectivity density, smaller clustering coefficients, and positive assortativity. Our results suggest that our method can characterize frequency dependent differences of network architecture from different brain regions. Crucially, because these differences between brain regions require millisecond temporal scales to be observed and characterized, these results underscore the importance of high temporal resolution recordings for the understanding of functional networks in neuronal systems. © 2014 Ito et al.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectanimal experiment
dc.subjectanimal tissue
dc.subjectarticle
dc.subjectbrain cortex
dc.subjectbrain region
dc.subjectbrain slice
dc.subjectconnectome
dc.subjectcontrolled study
dc.subjecthippocampus
dc.subjectimmunohistochemistry
dc.subjectmouse
dc.subjectnerve cell network
dc.subjectnervous tissue
dc.subjectnonhuman
dc.subjectrating scale
dc.subjectsomatosensory cortex
dc.subjectwavelet analysis
dc.subjectaction potential
dc.subjectanimal
dc.subjectC57BL mouse
dc.subjectcomparative study
dc.subjectcytology
dc.subjectelectroencephalography
dc.subjectfemale
dc.subjecthippocampus
dc.subjectmale
dc.subjectphysiology
dc.subjecttissue culture technique
dc.subjectAction Potentials
dc.subjectAnimals
dc.subjectElectroencephalography
dc.subjectFemale
dc.subjectHippocampus
dc.subjectMale
dc.subjectMice, Inbred C57BL
dc.subjectNerve Net
dc.subjectTissue Culture Techniques
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1371/journal.pone.0105324
dc.description.sourcetitlePLoS ONE
dc.description.volume9
dc.description.issue8
dc.description.pagee105324
dc.published.statePublished
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