Inhibition of in vitro chondrogenesis in RGD-modified three-dimensional alginate gels

被引:163
作者
Connelly, John T. [1 ]
Garcia, Andres J. [1 ]
Levenston, Marc E. [1 ]
机构
[1] Georgia Inst Technol, George W Woodruff Sch Mech Engn, Parker H Petit Inst Bioengn & Biosci, Atlanta, GA 30332 USA
关键词
alginate; cartilage tissue engineering; mesenchymal stem cell; integrin; RGD peptide; TGF;
D O I
10.1016/j.biomaterials.2006.10.006
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
The goal of this study was to investigate the effects of adhesion to the arginine-glycine-aspartic acid (RGD) sequence on the chondrogenesis of bone marrow stromal cells (BMSCs). Synthetic RGE- and RGD-containing peptides were conjugated to sodium alginate, and bovine BMSCs were seeded onto 2D alginate surfaces or encapsulated in 3D gels. BMSCs spread specifically on RGD-modified surfaces, and spreading was inhibited by a soluble RGD peptide and by anti-beta 1 and anti-alpha v beta 3 integrin blocking antibodies. After 7 days in 3D gel culture, the chondrogenic supplements (TGF-beta 1 and dexamethasone) significantly stimulated chondrocytic gene expression (collagen II, aggrecan, and Sox-9) and matrix accumulation (collagen II and sGAG) in RGE-modified gels, but this response was inhibited in the RGD-modified gels. Inhibition of sGAG synthesis increased with increasing RGD density, and synthesis was partially rescued by adding a soluble RGD peptide. Addition of an anti-alpha v beta 3 integrin blocking antibody had no effect on chondrogenesis, while an anti-alpha 5 antibody reduced sGAG accumulation. Overall, this study demonstrates that interaction with the RGD motif significantly inhibits the initial chondrogenesis of BMSCs within 3D alginate gels. These results provide new insights into the role of cell-matrix interactions in regulating chondrogenesis and highlight the importance of choosing appropriate biomaterials for tissue engineering therapies. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1071 / 1083
页数:13
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