Biochemical composition and turnover of the extracellular matrix of the normal and degenerate intervertebral disc

Sarit Sara Sivan*, Anthony J. Hayes, Ellen Wachtel, Bruce Caterson, Yulia Merkher, Alice Maroudas, Sharon Brown, Sally Roberts

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

107 Citations (Scopus)

Abstract

Background: The intervertebral disc (IVD) is a complex cartilaginous structure which functions to resist biomechanical loads during spinal movement. It consists of the highly viscous cartilaginous nucleus pulposus, which is surrounded laterally by a thick outer ring of fibrous cartilage - the annulus fibrosus - and sandwiched inferiorly and superiorly by the cartilage end-plates. The main extracellular matrix molecules of the disc are collagens, proteoglycans, glycoproteins and elastin. The disc also contains appreciable amounts of water, matrix-degrading protease enzymes and their inhibitors, soluble signalling molecules and various metabolic breakdown products. Methods: This review provides a comprehensive description of the biochemical composition of the extracellular matrix of the IVD and, specifically, the proteases involved in its molecular turnover. Quantitation of the turnover rates using racemization of aspartic acid as a molecular clock is also discussed. Conclusions: Molecular turnover rates of the major constituent matrix macromolecules of the IVD are found to be particularly slow, especially in the case of collagen. Over a normal human life span, this slow turnover may compromise the structural integrity of the IVD extracellular matrix essential for normal physiological functioning.

Original languageEnglish
Pages (from-to)S344-S353
JournalEuropean Spine Journal
Volume23
Issue numberSUPPL. 3
DOIs
Publication statusPublished - Jun 2014

Funding

European Community [HEALTH-F2-2008-201626, FP7-People-2007-2-2-ERG, 224834]; Charles W. McCutchen FoundationAuthors would like to thank Dr. Michelle Kumin for her help and suggestions in writing this article. They are grateful to EA Kerr and J Menage for help in preparation of the manuscript. The research leading to these results has received funding from the European Community's Seventh Framework Programme (FP7, 2007-2013) under grant agreement no. HEALTH-F2-2008-201626 (Genodisc) and FP7-People-2007-2-2-ERG (grant agreement 224834). A.M.S.S. and Y.M acknowledge support from the Charles W. McCutchen Foundation.

All Science Journal Classification (ASJC) codes

  • Surgery
  • Orthopedics and Sports Medicine

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