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Co-culture of mechanically injured cartilage with joint capsule tissue alters chondrocyte expression patterns and increases ADAMTS5 production

Author(s)
Grodzinsky, Alan J.; Lee, J. H.; Fitzgerald, J. B.; DiMicco, M. A.; Cheng, D. M.; Flannery, C. R.; Sandy, J. D.; Plaas, A. H.; ... Show more Show less
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Abstract
We studied changes in chondrocyte gene expression, aggrecan degradation, and aggrecanase production and activity in normal and mechanically injured cartilage co-cultured with joint capsule tissue. Chondrocyte expression of 21 genes was measured at 1, 2, 4, 6, 12, and 24 h after treatment; clustering analysis enabled identification of co-expression profiles. Aggrecan fragments retained in cartilage and released to medium and loss of cartilage sGAG were quantified. Increased expression of MMP-13 and ADAMTS4 clustered with effects of co-culture, while increased expression of ADAMTS5, MMP-3, TGF-β, c-fos, c-jun clustered with cartilage injury. ADAMTS5 protein within cartilage (immunohistochemistry) increased following injury and with co-culture. Cartilage sGAG decreased over 16-days, most severely following injury plus co-culture. Cartilage aggrecan was cleaved at aggrecanase sites in the interglobular and C-terminal domains, resulting in loss of the G3 domain, especially after injury plus co-culture. Together, these results support the hypothesis that interactions between injured cartilage and other joint tissues are important in matrix catabolism after joint injury.
Date issued
2009-09
URI
http://hdl.handle.net/1721.1/66582
Department
Massachusetts Institute of Technology. Center for Biomedical Engineering; Massachusetts Institute of Technology. Department of Biological Engineering
Journal
Archives of Biochemistry and Biophysics
Publisher
Elsevier Ltd.
Citation
Lee, J.H. et al. “Co-culture of mechanically injured cartilage with joint capsule tissue alters chondrocyte expression patterns and increases ADAMTS5 production.” Archives of Biochemistry and Biophysics 489 (2009): 118-126. Web. 26 Oct. 2011. © 2009 Elsevier Inc.
Version: Author's final manuscript
ISSN
0003-9861

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