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Synaptic compartmentalization by micropatterned masking of a surface adhesive cue in cultured neurons

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dc.contributor.authorRyu, Jae Ryun-
dc.contributor.authorJang, Min Jee-
dc.contributor.authorJo, Youhwa-
dc.contributor.authorJoo, Sunghoon-
dc.contributor.authorLee, Do Hoon-
dc.contributor.authorLee, Byung Yang-
dc.contributor.authorNam, Yoonkey-
dc.contributor.authorSun, Woong-
dc.date.accessioned2021-09-03T23:10:21Z-
dc.date.available2021-09-03T23:10:21Z-
dc.date.created2021-06-18-
dc.date.issued2016-06-
dc.identifier.issn0142-9612-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/88406-
dc.description.abstractFunctions of neuronal circuit are fundamentally modulated by its quality and quantity of connections. Assessment of synapse, the basic unit for a neuronal connection, is labor-intensive and time-consuming in conventional culture systems, due to the small size and the spatially random distribution. In the present study, we propose a novel 'synapse compartmentalization' culture system, in which synapses are concentrated at controlled locations. We fabricated a negative dot array pattern by coating the entire surface with poly-l-lysine (PLL) and subsequent microcontact printing of 1) substrates which mask positive charge of NI (Fc, BSA and laminin), or 2) a chemorepulsive protein (Semaphorin 3F-Fc). By combination of physical and biological features of these repulsive substrates, functional synapses were robustly concentrated in the PLL-coated dots. This synapse compartmentalization chip can be combined with the various high-throughput assay formats based on the synaptic morphology and function. Therefore, this quantifiable and controllable dot array pattern by microcontact printing will be potential useful for bio-chip platforms for the high-density assays used in synapse-related neurobiological studies. (C) 2016 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCI LTD-
dc.subjectGUIDANCE-
dc.subjectGROWTH-
dc.subjectSPECIFICATION-
dc.subjectMATURATION-
dc.subjectMOLECULES-
dc.subjectMIGRATION-
dc.subjectPROTEIN-
dc.subjectRHO-
dc.titleSynaptic compartmentalization by micropatterned masking of a surface adhesive cue in cultured neurons-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Byung Yang-
dc.contributor.affiliatedAuthorSun, Woong-
dc.identifier.doi10.1016/j.biomaterials.2016.03.027-
dc.identifier.scopusid2-s2.0-84973534651-
dc.identifier.wosid000375366200005-
dc.identifier.bibliographicCitationBIOMATERIALS, v.92, pp.46 - 56-
dc.relation.isPartOfBIOMATERIALS-
dc.citation.titleBIOMATERIALS-
dc.citation.volume92-
dc.citation.startPage46-
dc.citation.endPage56-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.subject.keywordPlusGUIDANCE-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusSPECIFICATION-
dc.subject.keywordPlusMATURATION-
dc.subject.keywordPlusMOLECULES-
dc.subject.keywordPlusMIGRATION-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusRHO-
dc.subject.keywordAuthorMicrocontact printing-
dc.subject.keywordAuthorSynapse compartmentalization-
dc.subject.keywordAuthorBioassay chip-
dc.subject.keywordAuthorNeuronal culture-
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