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Chondrogenesis of rabbit mesenchymal stem cells in fibrin/hyaluronan composite scaffold in vitro.

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dc.contributor.authorPark, SH-
dc.contributor.authorChoi, BH,-
dc.contributor.authorPark, SR-
dc.contributor.authorMin, BH-
dc.date.accessioned2012-05-09T05:11:46Z-
dc.date.available2012-05-09T05:11:46Z-
dc.date.issued2011-
dc.identifier.issn1937-3341-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/6878-
dc.description.abstractScaffold material is expected to play a crucial role in induction of chondrogenic differentiation of mesenchymal stem cells (MSCs) for cartilage tissue engineering. Here we demonstrated the feasibility of a fibrin/hyaluronan (HA) composite hydrogel as a potent scaffold for support of chondrogenesis of rabbit MSCs (rMSCs). rMSCs were prepared in three-dimensional cultures of pellet, alginate layer, and fibrin/HA gel. Specimens in each group were cultured in chondrogenic defined media for 4 weeks in the absence or presence of transforming growth factor β1 (TGF-β1) treatment. Viability of rMSCs was somewhat reduced until 4 weeks, which was less significant in fibrin/HA gels than in the alginate layer (*p < 0.05). The fibrin/HA group showed transient size reduction by about 35% at 1 week, but showed significantly higher mechanical strength than the alginate group. In safranin-O and alcian blue stains, accumulation of sulfated glycosaminoglycans (GAGs) was observed clearly from 1 week, and homogenously in the entire area at 4 weeks in the fibrin/HA group. Of note, TGF-β1 treatment showed no additional effect on GAGs accumulation in the fibrin/HA group. The alginate and pellet groups, however, showed much lower levels of GAGs accumulation only in the presence of TGF-β1. Biochemical assays for GAGs and collagen, and expression of chondrogenic markers also showed much better results in the fibrin/HA group, even without TGF-β treatment than the other groups. These results demonstrated that fibrin/HA composite gel efficiently promoted chondrogenic differentiation of rMSCs, even without TGF-β treatment, and that it could be a useful tool for use in cartilage tissue engineering.-
dc.language.isoen-
dc.subject.MESHAnimals-
dc.subject.MESHAntigens, Differentiation-
dc.subject.MESHCartilage-
dc.subject.MESHCells, Cultured-
dc.subject.MESHChondrogenesis-
dc.subject.MESHFibrin-
dc.subject.MESHHyaluronic Acid-
dc.subject.MESHMesenchymal Stem Cells-
dc.subject.MESHRabbits-
dc.subject.MESHTime Factors-
dc.subject.MESHTissue Engineering-
dc.subject.MESHTissue Scaffolds-
dc.subject.MESHTransforming Growth Factor beta1-
dc.titleChondrogenesis of rabbit mesenchymal stem cells in fibrin/hyaluronan composite scaffold in vitro.-
dc.typeArticle-
dc.identifier.pmid21189070-
dc.identifier.urlhttp://www.liebertonline.com/doi/abs/10.1089/ten.TEA.2010.0337?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%3dpubmed-
dc.contributor.affiliatedAuthor민, 병현-
dc.type.localJournal Papers-
dc.identifier.doi10.1089/ten.TEA.2010.0337-
dc.citation.titleTissue engineering. Part A-
dc.citation.volume17-
dc.citation.number9-10-
dc.citation.date2011-
dc.citation.startPage1277-
dc.citation.endPage1286-
dc.identifier.bibliographicCitationTissue engineering. Part A, 17(9-10). : 1277-1286, 2011-
dc.identifier.eissn1937-335X-
dc.relation.journalidJ019373341-
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Journal Papers > School of Medicine / Graduate School of Medicine > Orthopedic Surgery
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