Spatiotemporal Control of TGF-beta Signaling with Light

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dc.contributor.authorLi, Yuchaoko
dc.contributor.authorLee, Minjiko
dc.contributor.authorKim, Nuryko
dc.contributor.authorWu, Guoyuko
dc.contributor.authorDeng, Difanko
dc.contributor.authorKim, Jin Manko
dc.contributor.authorLiu, Xuedongko
dc.contributor.authorHeo, Won Doko
dc.contributor.authorZi, Zhikeko
dc.date.accessioned2018-03-23T00:16:05Z-
dc.date.available2018-03-23T00:16:05Z-
dc.date.created2018-03-20-
dc.date.created2018-03-20-
dc.date.created2018-03-20-
dc.date.issued2018-02-
dc.identifier.citationACS SYNTHETIC BIOLOGY, v.7, no.2, pp.443 - 451-
dc.identifier.issn2161-5063-
dc.identifier.urihttp://hdl.handle.net/10203/240950-
dc.description.abstractCells employ signaling pathways to make decisions in response to changes in their immediate environment. Transforming growth factor beta (TGF-beta) is an important growth factor that regulates many cellular functions in development and disease. Although the molecular mechanisms of TGF-beta signaling have been well studied, our understanding of this pathway is limited by the lack of tools that allow the control of TGF-beta signaling with high spatiotemporal resolution. Here, we developed an optogenetic system (optoTGFBRs) that enables the precise control of TGF-beta signaling in time and space. Using the optoTGFBRs system, we show that TGF-beta signaling can be selectively and sequentially activated in single cells through the modulation of the pattern of light stimulations. By simultaneously monitoring the subcellular localization of TGF-beta receptor and Smad2 proteins, we characterized the dynamics of TGF-beta signaling in response to different patterns of blue light stimulations. The spatial and temporal precision of light control will make the optoTGFBRs system as a powerful tool for quantitative analyses of TGF-beta signaling at the single cell level.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleSpatiotemporal Control of TGF-beta Signaling with Light-
dc.typeArticle-
dc.identifier.wosid000426012600017-
dc.identifier.scopusid2-s2.0-85042185959-
dc.type.rimsART-
dc.citation.volume7-
dc.citation.issue2-
dc.citation.beginningpage443-
dc.citation.endingpage451-
dc.citation.publicationnameACS SYNTHETIC BIOLOGY-
dc.identifier.doi10.1021/acssynbio.7b00225-
dc.contributor.localauthorHeo, Won Do-
dc.contributor.nonIdAuthorLi, Yuchao-
dc.contributor.nonIdAuthorKim, Nury-
dc.contributor.nonIdAuthorWu, Guoyu-
dc.contributor.nonIdAuthorDeng, Difan-
dc.contributor.nonIdAuthorKim, Jin Man-
dc.contributor.nonIdAuthorLiu, Xuedong-
dc.contributor.nonIdAuthorZi, Zhike-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorcell signaling-
dc.subject.keywordAuthorTGF-beta-
dc.subject.keywordAuthoroptogenetics-
dc.subject.keywordAuthorSmad2-
dc.subject.keywordPlusGROWTH-FACTOR-BETA-
dc.subject.keywordPlusOPTOGENETIC CONTROL-
dc.subject.keywordPlusMAMMALIAN-CELLS-
dc.subject.keywordPlusKINASE-ACTIVITY-
dc.subject.keywordPlusBLUE-LIGHT-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusINHIBITOR-
dc.subject.keywordPlusPATHWAY-
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