TNα-stimulated gene product (TSG-6) and its binding protein, IαI, in the human intervertebral disc:: new molecules for the disc

被引:30
作者
Roberts, S [1 ]
Evans, H
Menage, J
Urban, JPG
Bayliss, MT
Eisenstein, SM
Rugg, MS
Milner, CM
Griffin, S
Day, AJ
机构
[1] Robert Jones & Agnes Hunt Orthopaed Hosp, Ctr Spinal Studies, Oswestry SY10 7AG, Shrops, England
[2] Keele Univ, Oswestry SY10 7AG, Shrops, England
[3] Univ Oxford, Physiol Lab, Oxford OX1 3PT, England
[4] Univ London Royal Vet Coll, London, England
[5] Univ Oxford, MRC, Immunochem Unit, Oxford OX1 3QU, England
关键词
TSG-6; I alpha I; carrier proteins; tumour necrosis factor; intervertebral disc displacement; inflammation mediators;
D O I
10.1007/s00586-004-0798-x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Inflammation and irritation of the nerve roots has been indicated as an important factor in the pain associated with symptomatic disc herniations. Tumour necrosis factor alpha (TNF alpha) is now believed to be involved in this pathway. TNF alpha causes connective tissue cells in culture to synthesise a glycoprotein, TNF alpha-stimulated gene-6 (TSG-6). TSG-6 is found in inflammatory diseases of related connective tissues, such as articular cartilage in rheumatoid arthritis, but is not present in unaffected individuals. In order to determine if TSG-6 occurred in intervertebral disc ( and cartilage endplate), we have investigated the presence of TSG-6 and its binding protein, inter-alpha-inhibitor (I alpha I), in 58 herniated and 15 non-herniated discs. Immunostaining for the cytokines, IL-1 alpha, IL-1 beta and TNFa, has also been carried out. We have demonstrated that both TSG-6 and I alpha I occur commonly in human intervertebral disc matrix with at least some TSG-6 in 98% of discs studied and IaI in all of them. Staining for TSG-6 was greatest in herniated discs, particularly close to blood vessels. IaI immunostaining was frequently widespread throughout the disc but there was little in the cartilage endplate. It has been proposed that these molecules have widespread effects, including extracellular matrix stabilisation, downregulation of the protease network and reduction of inflammation. Hence, the occurrence of TSG-6 and IaI in disc tissue could have implications in the aetiopathogenesis and future therapeutics of intervertebral disc disease.
引用
收藏
页码:36 / 42
页数:7
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