The purpose of the Biomarker Core facility is to provide a comprehensive, centralized resource for biomarker analyses required for the evaluation of cartilage matrix metabolism and the role of inflammation in the pathogenesis of OA. This Core will serve all of the projects of the Program Project proposal which are linked by a common interest in the role of biomechanical factors and inflammation in modifying joint tissue metabolism and their contribution to osteoarthritis. The expertise offered through this core facility will permit molecular analyses of factors associated with cartilage matrix metabolism and inflammation from both animal and human samples including serum, synovial fluid, and urine. The Core offers the capability of measuring multiple analytes from small sample volumes with high sensitivity, which is especially useful for projects involving limited quantities of samples. In addition, the Core will coordinate collaboration with the Duke Stedman Nutrition Center to explore the utility of metabolomics for elucidating metabolic profiles in the high fat fed mice in Project 1. This information will be compared with the metabolomic profiles obtained from patients with knee OA participating in Project 3, funded through the Duke Aging Center. This novel and exciting approach will provide unique insights into the interactions of diet, obesity, and osteoarthritis. This Core will also serve as a resource for the training of investigators on principles and methods of biomarker analyses. We anticipate that this Core will stimulate collaborative interaction and facilitate the testing of central hypotheses related to this OA Program Project. Relevance to Public Health: This Biomarkers Core provides state-of-the-art analyses of joint tissue and inflammation markers. These markers, tested across all of the projects, provide a unique opportunity to understand the relationship of obesity and inflammation in osteoarthritis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Program Projects (P01)
Project #
5P01AR050245-09
Application #
8327288
Study Section
Special Emphasis Panel (ZAR1)
Project Start
2011-09-01
Project End
2013-08-31
Budget Start
2011-09-01
Budget End
2012-08-31
Support Year
9
Fiscal Year
2011
Total Cost
$116,607
Indirect Cost
Name
Duke University
Department
Type
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Guilak, Farshid; Nims, Robert J; Dicks, Amanda et al. (2018) Osteoarthritis as a disease of the cartilage pericellular matrix. Matrix Biol 71-72:40-50
Rowland, Christopher R; Glass, Katherine A; Ettyreddy, Adarsh R et al. (2018) Regulation of decellularized tissue remodeling via scaffold-mediated lentiviral delivery in anatomically-shaped osteochondral constructs. Biomaterials 177:161-175
Furman, Bridgette D; Kent, Collin L; Huebner, Janet L et al. (2018) CXCL10 is upregulated in synovium and cartilage following articular fracture. J Orthop Res 36:1220-1227
Erdemir, Ahmet; Hunter, Peter J; Holzapfel, Gerhard A et al. (2018) Perspectives on Sharing Models and Related Resources in Computational Biomechanics Research. J Biomech Eng 140:
Collins, Amber T; Kulvaranon, Micaela L; Cutcliffe, Hattie C et al. (2018) Obesity alters the in vivo mechanical response and biochemical properties of cartilage as measured by MRI. Arthritis Res Ther 20:232
Brunger, Jonathan M; Zutshi, Ananya; Willard, Vincent P et al. (2017) CRISPR/Cas9 Editing of Murine Induced Pluripotent Stem Cells for Engineering Inflammation-Resistant Tissues. Arthritis Rheumatol 69:1111-1121
Wu, Chia-Lung; McNeill, Jenna; Goon, Kelsey et al. (2017) Conditional Macrophage Depletion Increases Inflammation and Does Not Inhibit the Development of Osteoarthritis in Obese Macrophage Fas-Induced Apoptosis-Transgenic Mice. Arthritis Rheumatol 69:1772-1783
Gruss, Laura Tobias; Gruss, Richard; Schmitt, Daniel (2017) Pelvic Breadth and Locomotor Kinematics in Human Evolution. Anat Rec (Hoboken) 300:739-751
Brunger, Jonathan M; Zutshi, Ananya; Willard, Vincent P et al. (2017) Genome Engineering of Stem Cells for Autonomously Regulated, Closed-Loop Delivery of Biologic Drugs. Stem Cell Reports 8:1202-1213
Hatcher, Courtney C; Collins, Amber T; Kim, Sophia Y et al. (2017) Relationship between T1rho magnetic resonance imaging, synovial fluid biomarkers, and the biochemical and biomechanical properties of cartilage. J Biomech 55:18-26

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