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Pericellular colocalisation and interactive properties of type VI collagen and perlecan in the intervertebral disc.

Authors :
Hayes AJ
Shu CC
Lord MS
Little CB
Whitelock JM
Melrose J
Source :
European cells & materials [Eur Cell Mater] 2016 Jul 05; Vol. 32, pp. 40-57. Date of Electronic Publication: 2016 Jul 05.
Publication Year :
2016

Abstract

The aim of this study was to immunolocalise type VI collagen and perlecan and determine their interactive properties in the intervertebral disc (IVD). Confocal laser scanning microscopy co-localised perlecan with type VI collagen as pericellular components of IVD cells and translamellar cross-bridges in ovine and murine IVDs. These cross-bridges were significantly less abundant in the heparin sulphate deficient Hspg2 exon 3 null mouse IVD than in wild type. This association of type VI collagen with elastic components provides clues as to its roles in conveying elastic recoil properties to annular tissues. Perlecan and type VI collagen were highly interactive in plasmon resonance studies. Pericellular colocalisation of perlecan and type VI collagen provides matrix stabilisation and cell-matrix communication which allows IVD cells to perceive and respond to perturbations in their biomechanical microenvironment. Perlecan, at the cell surface, provides an adhesive interface between the cell and its surrounding extracellular matrix. Elastic microfibrillar structures regulate tensional connective tissue development and function. The 2010 Global Burden of Disease study examined 291 disorders and identified disc degeneration and associated low back pain as the leading global musculoskeletal disorder emphasising its massive socioeconomic impact and the need for more effective treatment strategies. A greater understanding of how the IVD achieves its unique biomechanical functional properties is of great importance in the development of such therapeutic measures.

Details

Language :
English
ISSN :
1473-2262
Volume :
32
Database :
MEDLINE
Journal :
European cells & materials
Publication Type :
Academic Journal
Accession number :
27377666
Full Text :
https://doi.org/10.22203/ecm.v032a03