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Enhanced chondrogenic marker expression of human mesenchymal stem cells by interaction with both TGF-beta 3 and hyaluronic acid

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dc.contributor.authorBhang, Suk Ho-
dc.contributor.authorJeon, Jeong-Yi-
dc.contributor.authorLa, Wan-Geun-
dc.contributor.authorSeong, Jun Yeup-
dc.contributor.authorHwang, Jin Wook-
dc.contributor.authorRyu, Seong Eon-
dc.contributor.authorKim, Byung-Soo-
dc.date.accessioned2022-07-16T19:56:35Z-
dc.date.available2022-07-16T19:56:35Z-
dc.date.created2021-05-12-
dc.date.issued2011-07-
dc.identifier.issn0885-4513-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/168058-
dc.description.abstractThis study was designed to evaluate the additive effects of transforming growth factor-beta3 (TGF-beta 3) and hyaluronic acid (HA) on chondrogenic differentiation of human mesenchymal stem cells (hMSCs). The hMSCs were cultured on collagen type I-, HA-, or fibronectin-coated cell culture dishes with or without TGF-beta 3 added to the culture medium. Four weeks after cell culture, chondrogenic differentiation of hMSCs was determined by evaluating the expression of cartilage-specific markers using real-time polymerase chain reaction, immunocytochemistry, and Western blot analysis. hMSCs cultured on HA-coated dishes with TGF-beta 3 supplementation revealed a prominent increase in collagen type II, aggrecan, and Sox9. When hMSCs were cultured without TGF-beta 3 supplementation, only hMSCs cultured on HA-coated dishes showed prominent expression of the cartilage-specific markers. This study shows that chondrogenic differentiation of hMSCs can be enhanced additively by interactions with both a specific cell-adhesion matrix and a soluble growth factor.-
dc.language영어-
dc.language.isoen-
dc.publisherWILEY-
dc.titleEnhanced chondrogenic marker expression of human mesenchymal stem cells by interaction with both TGF-beta 3 and hyaluronic acid-
dc.typeArticle-
dc.contributor.affiliatedAuthorRyu, Seong Eon-
dc.identifier.doi10.1002/bab.39-
dc.identifier.scopusid2-s2.0-80051779230-
dc.identifier.wosid000294583700009-
dc.identifier.bibliographicCitationBIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, v.58, no.4, pp.271 - 276-
dc.relation.isPartOfBIOTECHNOLOGY AND APPLIED BIOCHEMISTRY-
dc.citation.titleBIOTECHNOLOGY AND APPLIED BIOCHEMISTRY-
dc.citation.volume58-
dc.citation.number4-
dc.citation.startPage271-
dc.citation.endPage276-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.subject.keywordPlusAUTOLOGOUS CHONDROCYTE TRANSPLANTATION-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusCARTILAGE-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusMATRIX-
dc.subject.keywordPlusBONE-
dc.subject.keywordPlusKNEE-
dc.subject.keywordPlusDEDIFFERENTIATION-
dc.subject.keywordPlusIMPLANTATION-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordAuthorchondrogenesis-
dc.subject.keywordAuthorhuman mesenchymal stem cells-
dc.subject.keywordAuthorhyaluronic acid-
dc.subject.keywordAuthortransforming growth factor-beta3-
dc.identifier.urlhttps://iubmb.onlinelibrary.wiley.com/doi/10.1002/bab.39-
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