Engineering Endostatin-Producing Cartilaginous Constructs for Cartilage Repair Using Nonviral Transfection of Chondrocyte-Seeded and Mesenchymal-Stem-Cell-Seeded Collagen Scaffolds

Although there is widespread recognition of the importance of angiogenesis in tissue repair, there is little work on the inhibition of angiogenesis in the context of tissue engineering of naturally avascular tissues, like articular cartilage. The objective was to engineer a collagen-scaffold-based c...

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Bibliographic Details
Main Authors: Jeng, Lily (Contributor), Olsen, Bjorn R. (Author), Spector, Myron (Contributor)
Other Authors: Harvard University- (Contributor), Massachusetts Institute of Technology. Department of Biological Engineering (Contributor)
Format: Article
Language:English
Published: Mary Ann Liebert, 2011-03-11T21:26:56Z.
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Online Access:Get fulltext
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100 1 0 |a Jeng, Lily  |e author 
100 1 0 |a Harvard University-  |e contributor 
100 1 0 |a Massachusetts Institute of Technology. Department of Biological Engineering  |e contributor 
100 1 0 |a Spector, Myron  |e contributor 
100 1 0 |a Jeng, Lily  |e contributor 
100 1 0 |a Spector, Myron  |e contributor 
700 1 0 |a Olsen, Bjorn R.  |e author 
700 1 0 |a Spector, Myron  |e author 
245 0 0 |a Engineering Endostatin-Producing Cartilaginous Constructs for Cartilage Repair Using Nonviral Transfection of Chondrocyte-Seeded and Mesenchymal-Stem-Cell-Seeded Collagen Scaffolds 
260 |b Mary Ann Liebert,   |c 2011-03-11T21:26:56Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/61686 
520 |a Although there is widespread recognition of the importance of angiogenesis in tissue repair, there is little work on the inhibition of angiogenesis in the context of tissue engineering of naturally avascular tissues, like articular cartilage. The objective was to engineer a collagen-scaffold-based cartilaginous construct overexpressing a potent antiangiogenic factor, endostatin, using nonviral transfection. Endostatin-plasmid-supplemented collagen scaffolds were seeded with mesenchymal stem cells and chondrocytes and cultured for 20-22 days. The effects of the following variables on endostatin expression and chondrogenesis were examined: collagen scaffold material, method of nonviral vector incorporation, plasmid load, culture medium, and oxygen tension. An increase and peak of endostatin protein was observed during the first week of culture, followed by a decrease to low levels, suggesting that overexpression of endostatin could be sustained for several days using the nonviral vector. The amount of endostatin produced was tunable with the external factors. Chondrogenesis was observed in the engineered constructs cultured in chondrogenic medium at the 3-week time point, demonstrating that endostatin did not inhibit the chondrogenic potential of mesenchymal stem cells or the general viability of the cells. The ability to engineer endostatin-expressing cartilaginous constructs will be of value for future work exercising regulatory control of angiogenesis in cartilage repair. 
520 |a United States. Dept. of Veterans Affairs. Rehabilitation Research and Development Service 
520 |a United States. Dept. of Defense 
520 |a National Science Foundation (U.S.). Graduate Research Fellowship Program 
546 |a en_US 
655 7 |a Article 
773 |t Tissue Engineering. Part A