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dc.contributor.authorTsuda, Sachiko-
dc.contributor.authorKee, Michelle Z. L.-
dc.contributor.authorCunha, Catarina-
dc.contributor.authorKim, Jinsook-
dc.contributor.authorYan, Ping-
dc.contributor.authorLoew, Leslie M.-
dc.contributor.authorAugustine, George J.-
dc.date.accessioned2024-01-20T13:04:02Z-
dc.date.available2024-01-20T13:04:02Z-
dc.date.created2022-01-10-
dc.date.issued2013-01-
dc.identifier.issn0168-0102-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/128471-
dc.description.abstractRecent advances in our understanding of brain function have come from using light to either control or image neuronal activity. Here we describe an approach that combines both techniques: a micromirror array is used to photostimulate populations of presynaptic neurons expressing channelrhodopsin-2, while a red-shifted voltage-sensitive dye allows optical detection of resulting postsynaptic activity. Such technology allowed us to control the activity of cerebellar interneurons while simultaneously recording inhibitory responses in multiple Purkinje neurons, their postsynaptic targets. This approach should substantially accelerate our understanding of information processing by populations of neurons within brain circuits. (C) 2013 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER IRELAND LTD-
dc.subjectNEURAL ACTIVITY-
dc.subjectCEREBELLAR CORTEX-
dc.subjectTRANSGENIC MICE-
dc.subjectOPTICAL CONTROL-
dc.subjectINHIBITION-
dc.subjectINTERNEURONS-
dc.subjectINDICATOR-
dc.subjectCHANNELRHODOPSIN-2-
dc.subjectINTERROGATION-
dc.subjectOSCILLATIONS-
dc.titleProbing the function of neuronal populations: Combining micromirror-based optogenetic photostimulation with voltage-sensitive dye imaging-
dc.typeArticle-
dc.identifier.doi10.1016/j.neures.2012.11.006-
dc.description.journalClass1-
dc.identifier.bibliographicCitationNEUROSCIENCE RESEARCH, v.75, no.1, pp.76 - 81-
dc.citation.titleNEUROSCIENCE RESEARCH-
dc.citation.volume75-
dc.citation.number1-
dc.citation.startPage76-
dc.citation.endPage81-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000316435700013-
dc.identifier.scopusid2-s2.0-84875369070-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.type.docTypeArticle-
dc.subject.keywordPlusNEURAL ACTIVITY-
dc.subject.keywordPlusCEREBELLAR CORTEX-
dc.subject.keywordPlusTRANSGENIC MICE-
dc.subject.keywordPlusOPTICAL CONTROL-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusINTERNEURONS-
dc.subject.keywordPlusINDICATOR-
dc.subject.keywordPlusCHANNELRHODOPSIN-2-
dc.subject.keywordPlusINTERROGATION-
dc.subject.keywordPlusOSCILLATIONS-
dc.subject.keywordAuthorOptogenetics-
dc.subject.keywordAuthorChannelrhodopsin-
dc.subject.keywordAuthorDigital micromirror device-
dc.subject.keywordAuthorVoltage-sensitive dye imaging-
dc.subject.keywordAuthorInhibitory circuitry-
dc.subject.keywordAuthorCerebellum-
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