A model system for evaluating the role of specific molecules on the mechanical properties of cartilage matrix will be developed. Using methods of gene transfection and RNA interference, decorin will be either overexpressed or suppressed in chondrocytes from young rabbits, and then these cells grown in culture to produce a tissue that can be mechanically tested. Comparing mechanical test results from normal tissue with the gene altered tissue will aid in defining the role decorin, and other candidate molecules, plays in the mechanical properties of chondrocyte matrix. The developed model will be a new way to study the structure/function relationships for cartilage matrix molecules, and to study the mechanisms of cartilage diseases such as osteoarthritis. Cartilage weakens in the OA disease process; the new method will help identify critical molecules that when damaged could lead to this weakening.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AR050731-01
Application #
6729757
Study Section
Special Emphasis Panel (ZAR1-RJB-A (O1))
Program Officer
Tyree, Bernadette
Project Start
2003-09-25
Project End
2005-06-30
Budget Start
2003-09-25
Budget End
2004-06-30
Support Year
1
Fiscal Year
2003
Total Cost
$74,250
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Orthopedics
Type
Schools of Medicine
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Lewis, Jack L; Krawczak, David A; Oegema Jr, Ted R et al. (2010) Effect of decorin and dermatan sulfate on the mechanical properties of a neocartilage. Connect Tissue Res 51:159-70
Hall, M L; Krawczak, D A; Simha, N K et al. (2009) Effect of dermatan sulfate on the indentation and tensile properties of articular cartilage. Osteoarthritis Cartilage 17:655-61