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Cited 22 time in webofscience Cited 21 time in scopus
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dc.contributor.authorAe Ryang Jung-
dc.contributor.authorRichard Y. Kim-
dc.contributor.authorHyung Woo Kim-
dc.contributor.authorKshitiz Raj Shrestha-
dc.contributor.authorSeung Hwan Jeon-
dc.contributor.authorKyoung Je Cha-
dc.contributor.authorYong Hyun Park-
dc.contributor.authorKim, DS-
dc.contributor.authorJi Youl Lee-
dc.date.accessioned2016-04-01T07:34:38Z-
dc.date.available2016-04-01T07:34:38Z-
dc.date.created2015-07-31-
dc.date.issued2015-07-
dc.identifier.issn1937-3341-
dc.identifier.other2015-OAK-0000033491-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/26650-
dc.description.abstractHuman adipose-derived stem cells (hADSCs) can differentiate into various cell types depending on chemical and topographical cues. One topographical cue recently noted to be successful in inducing differentiation is the nanoengineered polystyrene surface containing nanopore array-patterned substrate (NP substrate), which is designed to mimic the nanoscale topographical features of the extracellular matrix. In this study, efficacies of NP and flat substrates in inducing neural differentiation of hADSCs were examined by comparing their substrate-cell adhesion rates, filopodia growth, nuclei elongation, and expression of neural-specific markers. The polystyrene nano Petri dishes containing NP substrates were fabricated by a nano injection molding process using a nickel electroformed nano-mold insert (Diameter: 200nm. Depth of pore: 500nm. Center-to-center distance: 500nm). Cytoskeleton and filopodia structures were observed by scanning electron microscopy and F-actin staining, while cell adhesion was tested by vinculin staining after 24 and 48h of seeding. Expression of neural specific markers was examined by real-time quantitative polymerase chain reaction and immunocytochemistry. Results showed that NP substrates lead to greater substrate-cell adhesion, filopodia growth, nuclei elongation, and expression of neural specific markers compared to flat substrates. These results not only show the advantages of NP substrates, but they also suggest that further study into cell-substrate interactions may yield great benefits for biomaterial engineering.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherMARY ANN LIEBERT, INC-
dc.relation.isPartOfTISSUE ENGINEERING PART A-
dc.titleNanoengineered Polystyrene Surfaces with Nanopore Array Pattern Alters Cytoskeleton Organization and Enhances Induction of Neural Differentiation of Human Adipose-Derived Stem Cells-
dc.typeArticle-
dc.contributor.college기계공학과-
dc.identifier.doi10.1089/TEN.TEA.2014.0346-
dc.author.googleJung A.R., Kim R.Y., Kim H.W., Shrestha K.R., Jeon S.H., Cha K.J., Park Y.H., Kim D.S., Lee J.Y.-
dc.relation.volume21-
dc.relation.issue13-
dc.relation.startpage2115-
dc.relation.lastpage2124-
dc.contributor.id10170232-
dc.relation.journalTISSUE ENGINEERING PART A-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationTISSUE ENGINEERING PART A, v.21, no.13, pp.2115 - 2124-
dc.identifier.wosid000363982900015-
dc.date.tcdate2019-02-01-
dc.citation.endPage2124-
dc.citation.number13-
dc.citation.startPage2115-
dc.citation.titleTISSUE ENGINEERING PART A-
dc.citation.volume21-
dc.contributor.affiliatedAuthorKim, DS-
dc.identifier.scopusid2-s2.0-84936873888-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc11-
dc.description.scptc8*
dc.date.scptcdate2018-05-121*
dc.description.isOpenAccessN-
dc.type.docTypeArticle-
dc.subject.keywordPlusADHESION-
dc.subject.keywordPlusNANOSCALE-
dc.subject.keywordPlusTOPOGRAPHY-
dc.subject.keywordPlusSUBSTRATE-
dc.subject.keywordPlusFATE-
dc.relation.journalWebOfScienceCategoryCell & Tissue Engineering-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-

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김동성KIM, DONG SUNG
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