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dc.contributor.authorKolb, Ilya
dc.contributor.authorWang, Michael
dc.contributor.authorKodandaramaiah, Suhasa B.
dc.contributor.authorForest, Craig R.
dc.contributor.authorSinger, Annabelle C.
dc.contributor.authorTalei Franzesi, Giovanni
dc.contributor.authorBoyden, Edward
dc.date.accessioned2018-10-11T19:17:58Z
dc.date.available2018-10-11T19:17:58Z
dc.date.issued2018-02
dc.date.submitted2017-12
dc.identifier.issn0270-6474
dc.identifier.issn1529-2401
dc.identifier.urihttp://hdl.handle.net/1721.1/118445
dc.description.abstractRepeated sequences of neural activity are a pervasive feature of neural networks in vivo and in vitro. In the hippocampus, sequential firing of many neurons over periods of 100-300 ms reoccurs during behavior and during periods of quiescence. However, it is not known whether the hippocampus produces longer sequences of activity or whether such sequences are restricted to specific network states. Furthermore, whether long repeated patterns of activity are transmitted to single cells downstream is unclear. To answer these questions, we recorded intracellularly from hippocampal CA1 of awake, behaving male mice to examine both subthreshold activity and spiking output in single neurons. In eight of nine recordings, we discovered long (900 ms) reoccurring subthreshold fluctuations or “repeats.” Repeats generally were high-amplitude, nonoscillatory events reoccurring with 10msprecision. Using statistical controls, we determined that repeats occurred more often than would be expected from unstructured network activity (e.g., by chance). Most spikes occurred during a repeat, and when a repeat contained a spike, the spike reoccurred with precision on the order of ≤ 20 ms, showing that long repeated patterns of subthreshold activity are strongly connected to spike output. Unexpectedly, we found that repeats occurred independently of classic hippocampal network states like theta oscillations or sharp-wave ripples. Together, these results reveal surprisingly long patterns of repeated activity in the hippocampal network that occur nonstochastically, are transmitted to single downstream neurons, and strongly shape their output. This suggests that the timescale of information transmission in the hippocampal network is much longer than previously thought. Keywords: hippocampus; intracellular activity; subthreshold patternsen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Award 1DP1-NS-087724)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Award 1R01-MH-103910)en_US
dc.publisherSociety for Neuroscienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1523/JNEUROSCI.1519-17.2017en_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceFrontiersen_US
dc.titleEvidence for Long-Timescale Patterns of Synaptic Inputs in CA1 of Awake Behaving Miceen_US
dc.typeArticleen_US
dc.identifier.citationKolb, Ilya et al. “Evidence for Long-Timescale Patterns of Synaptic Inputs in CA1 of Awake Behaving Mice.” The Journal of Neuroscience 38, 7 (December 2017): 1821–1834 © 2018 The Authorsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Media Laboratoryen_US
dc.contributor.departmentMcGovern Institute for Brain Research at MITen_US
dc.contributor.mitauthorTalei Franzesi, Giovanni
dc.contributor.mitauthorBoyden, Edward
dc.relation.journalJournal of Neuroscienceen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-09-25T17:00:50Z
dspace.orderedauthorsKolb, Ilya; Talei Franzesi, Giovanni; Wang, Michael; Kodandaramaiah, Suhasa B.; Forest, Craig R.; Boyden, Edward S.; Singer, Annabelle C.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-7132-8706
dc.identifier.orcidhttps://orcid.org/0000-0002-0419-3351
mit.licensePUBLISHER_CCen_US


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