Expression profiling of metalloproteinases and inhibitors in cartilage |
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Authors: | Lara Kevorkian David A. Young Clare Darrah Simon T. Donell Lee Shepstone Sarah Porter Sarah Brockbank Dylan R. Edwards rew E. Parker Ian M. Clark |
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Affiliation: | School of Biological Sciences and Medicine, University of East Anglia, Norwich;;Institute of Orthopaedics, Norfolk &Norwich University Hospital, Norwich;School of Biological Sciences and;Medicine, University of East Anglia, Norwich;;Respiratory &Inflammation Research, AstraZeneca, Cheshire, UK |
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Abstract: | Objective To profile the expression of all known members of the matrix metalloproteinase ( MMP ), a disintegrin and metalloproteinase with thrombospondin motifs ( ADAMTS ), and tissue inhibitor of metalloproteinases ( TIMP s) gene families in normal cartilage and that from patients with osteoarthritis (OA). Methods Human cartilage was obtained from femoral heads at joint replacement for either osteoarthritis or following fracture to the neck of femur. Total RNA was purified and expression of genes assayed using quantitative real-time PCR. Results Several members of the above gene families were regulated in OA. Genes increasing in expression in OA were: at P < 0.001, MMP-13 , MMP-28 , ADAMTS-16 ; at P < 0.01, MMP-9 , MMP-16 , ADAMTS-2 , ADAMTS-14 and at P < 0.05, MMP-2 , TIMP-3 , ADAMTS-12 . Genes decreasing in expression in OA were: at P < 0.001, MMP-1 , MMP-3 , ADAMTS-1 ; at P < 0.01, MMP-10 , TIMP-1 , ADAMTS-9 and at P < 0.05, TIMP-4 , ADAMTS-5 , ADAMTS-15 . Correlation analysis revealed that groups of genes across the gene families are co-expressed in cartilage. Conclusion This is the first comprehensive expression profile of all known MMP , ADAMTS and TIMP genes in cartilage. Patterns of expression provide a foundation on which to understand mechanisms of gene regulation in OA and potentially for refining the specificity of anti-proteolytic therapies. |
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