Glycosaminoglycan profiles of repair tissue formed following autologous chondrocyte implantation differ from control cartilage

被引:0
作者
Aarti Sharma
Lindsay D Wood
James B Richardson
Sally Roberts
Nicola J Kuiper
机构
[1] University of Keele,Institute of Science & Technology in Medicine (ISTM)
[2] Robert Jones & Agnes Hunt (RJAH) Orthopaedic Hospital,Institute of Orthopaedics
[3] ISTM,Centre for Spinal Studies
[4] University of Keele,undefined
[5] RJAH Orthopaedic Hospital,undefined
[6] ISTM,undefined
[7] University of Keele,undefined
来源
Arthritis Research & Therapy | / 9卷
关键词
Articular Cartilage; Repair Tissue; Chondroitin Sulphate; Autologous Chondrocyte Implantation; Keratan Sulphate;
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摘要
Currently, autologous chondrocyte implantation (ACI) is the most commonly used cell-based therapy for the treatment of isolated femoral condyle lesions of the knee. A small number of centres performing ACI have reported encouraging long-term clinical results, but there is currently a lack of quantitative and qualitative biochemical data regarding the nature of the repair tissue. Glycosaminoglycan (GAG) structure influences physiological function and is likely to be important in the long-term stability of the repair tissue. The objective of this study was to use fluorophore-assisted carbohydrate electrophoresis (FACE) to both quantitatively and qualitatively analyse the GAG composition of repair tissue biopsies and compare them with age-matched cadaveric controls. We used immunohistochemistry to provide a baseline reference for comparison. Biopsies were taken from eight patients (22 to 52 years old) 1 year after ACI treatment and from four cadavers (20 to 50 years old). FACE quantitatively profiled the GAGs in as little as 5 μg of cartilage. The pattern and intensity of immunostaining were generally comparable with the data obtained with FACE. In the ACI repair tissue, there was a twofold reduction in chondroitin sulphate and keratan sulphate compared with age-matched control cartilage. By contrast, there was an increase in hyaluronan with significantly shorter chondroitin sulphate chains and less chondroitin 6-sulphate in repair tissue than control cartilage. The composition of the repair tissue thus is not identical to mature articular cartilage.
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