Source:http://linkedlifedata.com/resource/pubmed/id/16143394
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2005-11-9
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pubmed:abstractText |
Cartilage defects as a result of disease or injury have a very limited ability to heal spontaneously. Recently, tissue engineering and local therapeutic gene delivery systems have been paid much attention in the cartilage natural healing process. Gene-activated matrix (GAM) blends these two strategies, serving as local bioreactor with therapeutic agents expression and also providing a structural template to fill the lesion defects for cell adhesion, proliferation and synthesis of extracellular matrix (ECM). In the current study, we used chitosan-gelatin complex as biomaterials to fabricate three-dimensional scaffolds and plasmid DNA were entrapped in the scaffolds encoding transforming growth factor-beta1 (TGF-beta1), which has been proposed as a promoter of cartilage regeneration for its effect on the synthesis of matrix molecules and cell proliferation. The plasmid DNA incorporated in the scaffolds showed a burst release in the first week and a sustained release for the other 2 weeks. The gene transfectd into chondrocytes expresses TGF-beta1 protein stably in 3 weeks. The histological and immunohistochemical results confirmed that the primary chondrocytes cultured into the chitosan-gelatin scaffold maintained round and owned characters of high secretion of specific ECM. From this study, it can be concluded that this gene-activated chitosan-gelatins matrix has a potential in the application of cartilage defects regeneration.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Chitosan,
http://linkedlifedata.com/resource/pubmed/chemical/Coated Materials, Biocompatible,
http://linkedlifedata.com/resource/pubmed/chemical/Drug Carriers,
http://linkedlifedata.com/resource/pubmed/chemical/Gelatin,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0142-9612
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
27
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1095-103
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pubmed:dateRevised |
2006-11-20
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pubmed:meshHeading |
pubmed-meshheading:16143394-Animals,
pubmed-meshheading:16143394-Cell Proliferation,
pubmed-meshheading:16143394-Cells, Cultured,
pubmed-meshheading:16143394-Chitosan,
pubmed-meshheading:16143394-Chondrocytes,
pubmed-meshheading:16143394-Coated Materials, Biocompatible,
pubmed-meshheading:16143394-Diffusion,
pubmed-meshheading:16143394-Drug Carriers,
pubmed-meshheading:16143394-Gelatin,
pubmed-meshheading:16143394-Gene Transfer Techniques,
pubmed-meshheading:16143394-Humans,
pubmed-meshheading:16143394-Materials Testing,
pubmed-meshheading:16143394-Plasmids,
pubmed-meshheading:16143394-Porosity,
pubmed-meshheading:16143394-Proteins,
pubmed-meshheading:16143394-Rabbits
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pubmed:year |
2006
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pubmed:articleTitle |
Porous chitosan-gelatin scaffold containing plasmid DNA encoding transforming growth factor-beta1 for chondrocytes proliferation.
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pubmed:affiliation |
State Key Laboratory of Pharmaceutical Biotechnology, Department of Biochemistry, Nanjing University, Nanjing 210093, PR China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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