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Chondrogenesis of rabbit mesenchymal stem cells in fibrin/hyaluronan composite scaffold in vitro.
DC Field | Value | Language |
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dc.contributor.author | Park, SH | - |
dc.contributor.author | Choi, BH, | - |
dc.contributor.author | Park, SR | - |
dc.contributor.author | Min, BH | - |
dc.date.accessioned | 2012-05-09T05:11:46Z | - |
dc.date.available | 2012-05-09T05:11:46Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 1937-3341 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/6878 | - |
dc.description.abstract | Scaffold 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.iso | en | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Antigens, Differentiation | - |
dc.subject.MESH | Cartilage | - |
dc.subject.MESH | Cells, Cultured | - |
dc.subject.MESH | Chondrogenesis | - |
dc.subject.MESH | Fibrin | - |
dc.subject.MESH | Hyaluronic Acid | - |
dc.subject.MESH | Mesenchymal Stem Cells | - |
dc.subject.MESH | Rabbits | - |
dc.subject.MESH | Time Factors | - |
dc.subject.MESH | Tissue Engineering | - |
dc.subject.MESH | Tissue Scaffolds | - |
dc.subject.MESH | Transforming Growth Factor beta1 | - |
dc.title | Chondrogenesis of rabbit mesenchymal stem cells in fibrin/hyaluronan composite scaffold in vitro. | - |
dc.type | Article | - |
dc.identifier.pmid | 21189070 | - |
dc.identifier.url | http://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.affiliatedAuthor | 민, 병현 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1089/ten.TEA.2010.0337 | - |
dc.citation.title | Tissue engineering. Part A | - |
dc.citation.volume | 17 | - |
dc.citation.number | 9-10 | - |
dc.citation.date | 2011 | - |
dc.citation.startPage | 1277 | - |
dc.citation.endPage | 1286 | - |
dc.identifier.bibliographicCitation | Tissue engineering. Part A, 17(9-10). : 1277-1286, 2011 | - |
dc.identifier.eissn | 1937-335X | - |
dc.relation.journalid | J019373341 | - |
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