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Cell density-dependent differential proliferation of neural stem cells on omnidirectional nanopore-arrayed surface

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dc.contributor.authorCha, Kyoung Je-
dc.contributor.authorKong, Sun-Young-
dc.contributor.authorLee, Ji Soo-
dc.contributor.authorKim, Hyung Woo-
dc.contributor.authorShin, Jae-Yeon-
dc.contributor.authorLa, Moonwoo-
dc.contributor.authorHan, Byung Woo-
dc.contributor.authorKim, Dong Sung-
dc.contributor.authorKim, Hyun-Jung-
dc.date.available2019-03-08T07:38:36Z-
dc.date.issued2017-10-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/3780-
dc.description.abstractRecently, the importance of surface nanotopography in the determination of stem cell fate and behavior has been revealed. In the current study, we generated polystyrene cell-culture dishes with an omnidirectional nanopore arrayed surface (ONAS) (diameter: 200 nm, depth: 500 nm, center-to-center distance: 500 nm) and investigated the effects of nanotopography on rat neural stem cells (NSCs). NSCs cultured on ONAS proliferated better than those on the flat surface when cell density was low and showed less spontaneous differentiation during proliferation in the presence of mitogens. Interestingly, NSCs cultured on ONAS at clonal density demonstrated a propensity to generate neurospheres, whereas those on the flat surface migrated out, proliferated as individuals, and spread out to attach to the surface. However, the differential patterns of proliferation were cell density-dependent since the distinct phenomena were lost when cell density was increased. ONAS modulated cytoskeletal reorganization and inhibited formation of focal adhesion, which is generally observed in NSCs grown on flat surfaces. ONAS appeared to reinforce NSC-NSC interaction, restricted individual cell migration and prohibited NSC attachment to the nanopore surface. These data demonstrate that ONAS maintains NSCs as undifferentiated while retaining multipotency and is a better topography for culturing low density NSCs.-
dc.language영어-
dc.language.isoENG-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleCell density-dependent differential proliferation of neural stem cells on omnidirectional nanopore-arrayed surface-
dc.typeArticle-
dc.identifier.doi10.1038/s41598-017-13372-6-
dc.identifier.bibliographicCitationSCIENTIFIC REPORTS, v.7, no.1-
dc.description.isOpenAccessN-
dc.identifier.wosid000412950900013-
dc.identifier.scopusid2-s2.0-85031296812-
dc.citation.number1-
dc.citation.titleSCIENTIFIC REPORTS-
dc.citation.volume7-
dc.type.docTypeArticle-
dc.publisher.location영국-
dc.subject.keywordPlusEPIDERMAL GROWTH-FACTOR-
dc.subject.keywordPlusCENTRAL-NERVOUS-SYSTEM-
dc.subject.keywordPlusPROGENITOR CELLS-
dc.subject.keywordPlusAUTOCRINE/PARACRINE FACTOR-
dc.subject.keywordPlusSTEM/PROGENITOR CELLS-
dc.subject.keywordPlusEXTRACELLULAR-MATRIX-
dc.subject.keywordPlusSIGNALING PATHWAY-
dc.subject.keywordPlusSMALL-MOLECULE-
dc.subject.keywordPlusSELF-RENEWAL-
dc.subject.keywordPlusEXPRESSION-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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