Co-localization of insulin-like growth factor binding protein 3 and fibronectin in human articular cartilage

被引:31
作者
Martin, JA
Miller, BA
Scherb, MB
Lembke, LA
Buckwalter, JA
机构
[1] Univ Iowa, Coll Med, Dept Orthopaed, Iowa City, IA 52242 USA
[2] Iowa City Vet Adm Med Ctr, Iowa City, IA USA
关键词
D O I
10.1053/joca.2002.0791
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Objective: The anabolic cytokine insulin-like growth factor I (IGF-I) stimulates chondrocyte synthesis of matrix macromolecules and several lines of evidence suggest that it has a major role in maintaining articular cartilage and possibly in cartilage repair. Despite the apparent importance of IGF-I in articular cartilage metabolism and its potential importance in joint diseases, little is known about the regulation of IGF-I activity within the tissue. Insulin-like growth factor binding proteins (IGFBPs) bind IGF-I and can modify its activity. At least three IGFBPs are expressed by chondrocytes: IGFBP-3, -4 and -5. Localization of IGFPBs in the articular cartilage extracellular matrix (ECM) could create reservoirs of IGF-I within the articular cartilage ECM and thereby regulate local IGF-I levels. We hypothesized that ECM molecules bind and concentrate IGFPBs in the pericellular/territorial matrix. Design: Semi-quantitative immunohistological measures of co-localization were used to compare the spatial distribution of IGFBP-3, -4, and -5 with the distributions of three peri-cellularly-enriched matrix molecules fibronectin, tenascin-C, and type VI collagen in osteoarthritic and non-osteoarthritic human articular cartilage. Purified proteins were used in an agarose diffusion assay to compare IGFBP-3 binding to the same three matrix proteins. Results: IGFBP-3 associated with fibronectin in the pericellular/territorial matrix (similar to40% co-localization) but not with tenascin-C, or type VI collagen (-6% and -15% co-localization respectively, P<0.05). Neither IGFBP-4, nor IGFBP-5 were associated with any of the three ECM proteins (P<0.05). In agarose diffusion assays IGFBP-3 interacted with fibronectin and heparan sulfate proteoglycan but not with type VI collagen or tenascin-C. Conclusions: Direct binding between purified IGFBP-3 and fibronectin and the strong co-localization the two proteins in the cartilage matrix support the hypothesis that IGFPB-3 and fibronectin help regulate local IGF-I levels. (C) 2002 Published by Elsevier Science Ltd on behalf of OsteoArthritis Research Society International.
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页码:556 / 563
页数:8
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