Optogenetic Modulation of TrkB Signaling in the Mouse Brain

Cited 4 time in webofscience Cited 0 time in scopus
  • Hit : 242
  • Download : 47
DC FieldValueLanguage
dc.contributor.authorHong, Jongryulko
dc.contributor.authorHeo, Won Doko
dc.date.accessioned2020-04-02T09:20:04Z-
dc.date.available2020-04-02T09:20:04Z-
dc.date.created2020-03-30-
dc.date.created2020-03-30-
dc.date.created2020-03-30-
dc.date.created2020-03-30-
dc.date.issued2020-02-
dc.identifier.citationJOURNAL OF MOLECULAR BIOLOGY, v.432, no.4, pp.815 - 827-
dc.identifier.issn0022-2836-
dc.identifier.urihttp://hdl.handle.net/10203/273801-
dc.description.abstractOptogenetic activation of receptors has advantages compared with chemical or ligand treatment because of its high spatial and temporal precision. Especially in the brain, the use of a genetically encoded light-tunable receptor is superior to direct infusion or systemic drug treatment. We applied light-activatable TrkB receptors in the mouse brain with reduced basal activity by incorporating Cry2PHR mutant, Opto-cytTrkB(E281A). Upon AAV mediated gene delivery, this form was expressed at sufficient levels in the mouse hippocampus (HPC) and medial entorhinal cortex (MEC) retaining normal canonical signal transduction by the blue light stimulus, even by delivery of noninvasive LED light on the mouse head. Within target cells, where its expression was driven by a cell type-specific promoter, Opto-cytTrkB(E281A)-mediated TrkB signaling could be controlled by adjusting light-stimulating conditions. We further demonstrated that Opto-cytTrkB(E281A) could locally induce TrkB signaling in axon terminals in the MEC-HPC. In summary, Opto-cytTrkB(E281A) will be useful for elucidating time- and region-specific roles of TrkB signaling ranging from cellular function to neural circuit mechanisms.-
dc.languageEnglish-
dc.publisherACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD-
dc.titleOptogenetic Modulation of TrkB Signaling in the Mouse Brain-
dc.typeArticle-
dc.identifier.wosid000518867100004-
dc.identifier.scopusid2-s2.0-85078844657-
dc.type.rimsART-
dc.citation.volume432-
dc.citation.issue4-
dc.citation.beginningpage815-
dc.citation.endingpage827-
dc.citation.publicationnameJOURNAL OF MOLECULAR BIOLOGY-
dc.identifier.doi10.1016/j.jmb.2020.01.010-
dc.contributor.localauthorHeo, Won Do-
dc.description.isOpenAccessY-
dc.type.journalArticleArticle-
dc.subject.keywordAuthoroptogenetics-
dc.subject.keywordAuthorNtrk2-
dc.subject.keywordAuthorBDNF-
dc.subject.keywordAuthorTrkB-
dc.subject.keywordAuthorCry2PHR-
dc.subject.keywordPlusBDNF MESSENGER-RNA-
dc.subject.keywordPlusSPATIOTEMPORAL CONTROL-
dc.subject.keywordPlusSYNAPTIC PLASTICITY-
dc.subject.keywordPlusSPINE MORPHOLOGY-
dc.subject.keywordPlusCONSOLIDATION-
dc.subject.keywordPlusRECEPTORS-
dc.subject.keywordPlusLTP-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordPlusBETA-
Appears in Collection
BS-Journal Papers(저널논문)
Files in This Item
untitled.pdf(4.19 MB)Download
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 4 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0