pubmed-article:19235210 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19235210 | lifeskim:mentions | umls-concept:C1333569 | lld:lifeskim |
pubmed-article:19235210 | lifeskim:mentions | umls-concept:C1705126 | lld:lifeskim |
pubmed-article:19235210 | lifeskim:mentions | umls-concept:C1704423 | lld:lifeskim |
pubmed-article:19235210 | lifeskim:mentions | umls-concept:C1257975 | lld:lifeskim |
pubmed-article:19235210 | lifeskim:mentions | umls-concept:C1418601 | lld:lifeskim |
pubmed-article:19235210 | lifeskim:mentions | umls-concept:C0598067 | lld:lifeskim |
pubmed-article:19235210 | lifeskim:mentions | umls-concept:C1549859 | lld:lifeskim |
pubmed-article:19235210 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:19235210 | pubmed:dateCreated | 2009-12-23 | lld:pubmed |
pubmed-article:19235210 | pubmed:abstractText | We tested the in vitro feasibility of porous PCL (poly(epsilon-caprolactone)) as a scaffold for cartilage tissue engineering from mesenchymal stem cells (MSCs) and determined the effects of various surface treatments. Three porous PCL scaffold modifications were examined: (1) PCL/Pluronic F127, (2) PCL/collagen, and (3) PCL/Pluronic F127/collagen, in addition to (4) PCL-only. MSCs (5 x 10(5)) were seeded in PCL scaffolds of pore size 100-150 microm, and after 3 weeks of in vitro culture, MSC-scaffolds were investigated for gross appearance, DNA amount, glycosaminoglycan (GAG) content, chondrogenic gene expression, and histology. Grossly, the cell-scaffold complexes became harder, and were more easily manipulated with a forceps after 3 weeks of culture. The three surface-treated scaffolds had higher DNA contents than did the PCL-only scaffold, and the GAG contents in PCL/collagen and PCL/F127/collagen scaffolds were higher than those seen in the PCL-only scaffold. Real-time PCR showed that Sox-9 and COL2A1 mRNA levels were remarkably elevated in PCL/collagen and PCL/F127/collagen scaffolds versus the PCL-only scaffold. On the other hand, Col1A1 and Col10A1 mRNA levels were lower in the three modified PCL scaffolds than in the PCL-only scaffold. Histological findings generally concurred with GAG and RT-PCR findings, and demonstrated the affinity of PCL-based scaffolds for MSCs and the potentials of these scaffold to induce chondrogenic differentiation. Cells showed more differentiated appearance and more abundant extracellular matrix formation in PCL/collagen and PCL/collagen/F127 scaffolds. Our findings suggest that PCL-based porous scaffolds may be useful carriers for MSC transplantation in the cartilage tissue engineering field, and that collagen-based surface modifications further enhance the chondrogenic differentiation of MSCs. | lld:pubmed |
pubmed-article:19235210 | pubmed:language | eng | lld:pubmed |
pubmed-article:19235210 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19235210 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19235210 | pubmed:month | Feb | lld:pubmed |
pubmed-article:19235210 | pubmed:issn | 1552-4965 | lld:pubmed |
pubmed-article:19235210 | pubmed:author | pubmed-author:ImGun-IlGI | lld:pubmed |
pubmed-article:19235210 | pubmed:author | pubmed-author:KimHye-JoungH... | lld:pubmed |
pubmed-article:19235210 | pubmed:author | pubmed-author:LeeJin-HoJH | lld:pubmed |
pubmed-article:19235210 | pubmed:copyrightInfo | (c) 2009 Wiley Periodicals, Inc. | lld:pubmed |
pubmed-article:19235210 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19235210 | pubmed:volume | 92 | lld:pubmed |
pubmed-article:19235210 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19235210 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19235210 | pubmed:pagination | 659-66 | lld:pubmed |
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pubmed-article:19235210 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:19235210 | pubmed:articleTitle | Chondrogenesis using mesenchymal stem cells and PCL scaffolds. | lld:pubmed |
pubmed-article:19235210 | pubmed:affiliation | Department of Orthopaedics, Dongguk University International Hospital, 814 Siksa-dong, Goyang 410-773, Korea. | lld:pubmed |
pubmed-article:19235210 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19235210 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |