Literature DB >> 19180493

Modified expression of the ADAMTS enzymes and tissue inhibitor of metalloproteinases 3 during human intervertebral disc degeneration.

Aneta J Pockert1, Stephen M Richardson, Christine L Le Maitre, Malcolm Lyon, Jonathan A Deakin, David J Buttle, Anthony J Freemont, Judith A Hoyland.   

Abstract

OBJECTIVE: Intervertebral disc degeneration is linked to loss of extracellular matrix (ECM), particularly the early loss of aggrecan. A group of metalloproteinases called aggrecanases are important mediators of aggrecan turnover. The present study was undertaken to investigate the expression of the recognized aggrecanases and their inhibitor, tissue inhibitor of metalloproteinases 3 (TIMP-3), in human intervertebral disc tissue.
METHODS: Twenty-four nondegenerated and 30 degenerated disc samples were analyzed for absolute messenger RNA (mRNA) copy number of ADAMTS 1, 4, 5, 8, 9, and 15 and TIMP-3 by real-time reverse transcription-polymerase chain reaction. Thirty-six formalin-fixed embedded intervertebral disc samples of varying grades of degeneration were used for immunohistochemical analyses. In addition, samples from 8 subjects were analyzed for the presence of matrix metalloproteinase (MMP)- and aggrecanase-generated aggrecan products.
RESULTS: Messenger RNA for all the aggrecanases other than ADAMTS-8 was identified in intervertebral disc tissue, as was mRNA for TIMP-3. Levels of mRNA expression of ADAMTS 1, 4, 5, and 15 were significantly increased in degenerated tissue compared with nondegenerated tissue. All these aggrecanases and TIMP-3 were also detected immunohistochemically in disc tissue, and numbers of nucleus pulposus cells staining positive for ADAMTS 4, 5, 9, and 15 were significantly increased in degenerated tissue compared with nondegenerated tissue. Aggrecan breakdown products generated by MMP and aggrecanase activities were also detected in intervertebral disc tissue.
CONCLUSION: The aggrecanases ADAMTS 1, 4, 5, 9, and 15 may contribute to the changes occurring in the ECM during intervertebral disc degeneration. Targeting these enzymes may be a possible future therapeutic strategy for the prevention of intervertebral disc degeneration and its associated morbidity.

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Year:  2009        PMID: 19180493     DOI: 10.1002/art.24291

Source DB:  PubMed          Journal:  Arthritis Rheum        ISSN: 0004-3591


  94 in total

Review 1.  Diversity of intervertebral disc cells: phenotype and function.

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2.  Transcript levels of major MMPs and ADAMTS-4 in relation to the clinicopathological profile of patients with lumbar disc herniation.

Authors:  Alexandros Tsarouhas; Giannoula Soufla; Pavlos Katonis; Dritan Pasku; Antonis Vakis; Demetrios A Spandidos
Journal:  Eur Spine J       Date:  2010-09-22       Impact factor: 3.134

3.  Association of vitamin D receptor gene polymorphisms with disc degeneration.

Authors:  Adam Biczo; Julia Szita; Iain McCall; Peter Pal Varga; Aron Lazary
Journal:  Eur Spine J       Date:  2019-11-25       Impact factor: 3.134

Review 4.  Role of cytokines in intervertebral disc degeneration: pain and disc content.

Authors:  Makarand V Risbud; Irving M Shapiro
Journal:  Nat Rev Rheumatol       Date:  2013-10-29       Impact factor: 20.543

5.  Tumor necrosis factor-α- and interleukin-1β-dependent matrix metalloproteinase-3 expression in nucleus pulposus cells requires cooperative signaling via syndecan 4 and mitogen-activated protein kinase-NF-κB axis: implications in inflammatory disc disease.

Authors:  Xin Wang; Hua Wang; Hao Yang; Jun Li; Qiqing Cai; Irving M Shapiro; Makarand V Risbud
Journal:  Am J Pathol       Date:  2014-07-22       Impact factor: 4.307

Review 6.  Disc in flames: Roles of TNF-α and IL-1β in intervertebral disc degeneration.

Authors:  Z I Johnson; Z R Schoepflin; H Choi; I M Shapiro; M V Risbud
Journal:  Eur Cell Mater       Date:  2015-09-21       Impact factor: 3.942

Review 7.  An understanding of intervertebral disc development, maturation and cell phenotype provides clues to direct cell-based tissue regeneration therapies for disc degeneration.

Authors:  Ricardo Rodrigues-Pinto; Stephen M Richardson; Judith A Hoyland
Journal:  Eur Spine J       Date:  2014-04-29       Impact factor: 3.134

8.  Inflammatory cytokines induce NOTCH signaling in nucleus pulposus cells: implications in intervertebral disc degeneration.

Authors:  Hua Wang; Ye Tian; Jianru Wang; Kate L E Phillips; Abbie L A Binch; Sara Dunn; Alison Cross; Neil Chiverton; Zhaomin Zheng; Irving M Shapiro; Christine L Le Maitre; Makarand V Risbud
Journal:  J Biol Chem       Date:  2013-04-15       Impact factor: 5.157

9.  Transcriptional profiling of bovine intervertebral disc cells: implications for identification of normal and degenerate human intervertebral disc cell phenotypes.

Authors:  Ben M Minogue; Stephen M Richardson; Leo Ah Zeef; Anthony J Freemont; Judith A Hoyland
Journal:  Arthritis Res Ther       Date:  2010-02-11       Impact factor: 5.156

10.  Increased expression of matrix metalloproteinase-10, nerve growth factor and substance P in the painful degenerate intervertebral disc.

Authors:  Stephen M Richardson; Paul Doyle; Ben M Minogue; Kanna Gnanalingham; Judith A Hoyland
Journal:  Arthritis Res Ther       Date:  2009-08-20       Impact factor: 5.156

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