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dc.contributor.authorPark, Sang Eun-
dc.contributor.authorYeon, Gyu-Bum-
dc.contributor.authorGoo, Hui-Gwan-
dc.contributor.authorSeo, Dong Sik-
dc.contributor.authorDayem, Ahmed A.-
dc.contributor.authorLee, Kyung Eun-
dc.contributor.authorPark, Hyun-Mee-
dc.contributor.authorCho, Ssang-Goo-
dc.contributor.authorKim, Dae-Sung-
dc.date.accessioned2024-01-19T15:01:12Z-
dc.date.available2024-01-19T15:01:12Z-
dc.date.created2021-09-02-
dc.date.issued2021-05-
dc.identifier.issn0021-9541-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/117112-
dc.description.abstractPolyvinylidene fluoride (PVDF) is biocompatible, easy to fabricate, and has piezoelectric properties; it has been used for many biomedical applications including stem cell engineering. However, long-term cultivation of human embryonic stem cells (hESCs) and their differentiation toward cardiac lineages on PVDF have not been investigated. Herein, PVDF nanoscaled membrane scaffolds were fabricated by electrospinning; a vitronectin-derived peptide-mussel adhesive protein fusion (VNm) was immobilized on the scaffolds. hESCs cultured on the VNm-coated PVDF scaffold (VNm-PVDF scaffold) were stably expanded for more than 10 passages while maintaining the expression of pluripotency markers and genomic integrity. Under cardiac differentiation conditions, hESCs on the VNm-PVDF scaffold generated more spontaneously beating colonies and showed the upregulation of cardiac-related genes, compared with those cultured on Matrigel and VNm alone. Thus, VNm-PVDF scaffolds may be suitable for the long-term culture of hESCs and their differentiation into cardiac cells, thus expanding their application in regenerative medicine.-
dc.languageEnglish-
dc.publisherJohn Wiley & Sons Inc.-
dc.titleMaintenance and differentiation of human ES cells on polyvinylidene fluoride scaffolds immobilized with a vitronectin-derived peptide-
dc.typeArticle-
dc.identifier.doi10.1002/jcp.30095-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJournal of Cellular Physiology, v.236, no.5, pp.3510 - 3520-
dc.citation.titleJournal of Cellular Physiology-
dc.citation.volume236-
dc.citation.number5-
dc.citation.startPage3510-
dc.citation.endPage3520-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000576153200001-
dc.identifier.scopusid2-s2.0-85092200171-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaPhysiology-
dc.type.docTypeArticle-
dc.subject.keywordPlusADHESION-
dc.subject.keywordPlusPVDF-
dc.subject.keywordPlusBIOMATERIAL-
dc.subject.keywordPlusNANOFIBERS-
dc.subject.keywordPlusBEHAVIOR-
dc.subject.keywordAuthorcardiac differentiation-
dc.subject.keywordAuthorhuman embryonic stem cells-
dc.subject.keywordAuthorlong-term culture-
dc.subject.keywordAuthorpolyvinylidene fluoride-
dc.subject.keywordAuthorscaffolds-
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KIST Article > 2021
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