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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  • [1] Brittberg M(1994)Treatment of deep cartilage defects in the knee with autologous chondrocyte transplantation N Engl J Med 331 889-895
  • [2] Lindahl A(2000)Two- to 9-year outcome after autologous chondrocyte transplantation of the knee Clin Orthop Relat Res 374 212-234
  • [3] Nilsson A(1999)Repair of human articular cartilage after implantation of autologous chondrocytes J Bone Joint Surg Br 81 1064-1068
  • [4] Ohlsson C(2003)Autologous chondrocyte implantation for cartilage repair: monitoring its success by magnetic resonance imaging and histology Arthritis Res Ther 5 R60-R73
  • [5] Isaksson O(1997)Long-term results of rib perichondrial grafts for repair of cartilage defects in the human knee Int Orthop 21 313-317
  • [6] Peterson L(2006)A prospective, randomised study comparing two techniques of autologous chondrocyte implantation for osteochondral defects in the knee: periosteum covered versus type I/III collagen covered Knee 13 203-210
  • [7] Peterson L(2006)Magnetic resonance observation of cartilage repair tissue (MOCART) for the evaluation of autologous chondrocyte transplantation: determination of interobserver variability and correlation to clinical outcome after 2 years Eur J Radiol 57 16-23
  • [8] Minas T(2005)Comparative evaluation of autologous chondrocyte implantation and mosaicplasty: a multicentered randomized clinical trial Clin J Sport Med 15 220-226
  • [9] Brittberg M(1992)Proteoglycans: many forms and many functions FASEB J 6 861-870
  • [10] Nilsson A(1984)Fluid transport and mechanical properties of articular cartilage: a review J Biomech 17 377-394