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Modulation of human mesenchymal stem cell survival on electrospun mesh with co-immobilized epithelial growth factor and gelatin

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dc.contributor.authorShin, Young Min-
dc.contributor.authorLim, Jong-Young-
dc.contributor.authorPark, Jong-Seok-
dc.contributor.authorGwon, Hui-Jeong-
dc.contributor.authorJeong, Sung In-
dc.contributor.authorAhn, Sung-Jun-
dc.contributor.authorShin, Heungsoo-
dc.contributor.authorLim, Youn-Mook-
dc.date.accessioned2022-07-15T22:29:34Z-
dc.date.available2022-07-15T22:29:34Z-
dc.date.issued2015-06-
dc.identifier.issn2046-2069-
dc.identifier.issn2046-2069-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/157055-
dc.description.abstractIn this work, we present a biomimetic fibrous scaffold containing two biomolecules. A biocompatible poly(L-lactide-co-epsilon-caprolactone) mesh was fabricated by an electrospinning method, and then acrylic acid was grafted on the mesh to introduce a carboxyl group through gamma-ray irradiation. Subsequently, the epidermal growth factor (EGF) and gelatin were coupled to the mesh through the EDC reaction. The modified mesh presents a consistent fibre diameter (874.4 + 178.5 nm), with carboxyl groups (1.3 mM). EGF (171.7 ng mg(-1) mesh) and gelatin (67.2 +/- 30.5 mu g mg(-1) mesh) were successfully coupled on the mesh. The coupled EGF and gelatin promoted the cell viability 1.5- times higher than that from a non-modified mesh. In particular, the EGF on the meshes independently allowed hMSC to present a 3-times greater involucrin expression and enabled improved procollagen secretion, implying trans-differentiation of hMSC to keratinocyte-like cells. Therefore, the co-immobilization strategy of biomolecules using radiation technology may be an alternative tool for tissue engineering applications.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherRoyal Society of Chemistry-
dc.titleModulation of human mesenchymal stem cell survival on electrospun mesh with co-immobilized epithelial growth factor and gelatin-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1039/c5ra01626f-
dc.identifier.scopusid2-s2.0-84936804694-
dc.identifier.wosid000357803200040-
dc.identifier.bibliographicCitationRSC Advances, v.5, no.69, pp 55948 - 55956-
dc.citation.titleRSC Advances-
dc.citation.volume5-
dc.citation.number69-
dc.citation.startPage55948-
dc.citation.endPage55956-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusTISSUE ENGINEERING APPLICATIONS-
dc.subject.keywordPlusEXTRACELLULAR-MATRIX-
dc.subject.keywordPlusENDOTHELIAL-CELLS-
dc.subject.keywordPlusACRYLIC-ACID-
dc.subject.keywordPlusSCAFFOLDS-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusCOLLAGEN-
dc.subject.keywordPlusFABRICATION-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusNANOFIBER-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2015/RA/C5RA01626F-
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