Glycosaminoglycan turn-over in articular cartilage.

Glycosaminoglycan turn-over has been studied both in vivo and in vitro, by using sodium [35S]sulphate as a precursor. The in vivo experiments were performed on rabbits and dogs, taking special care to monitor the 35S radioactivity in the serum throughout the experiment and to measure the radioactivity due to unincorporated inorganic [35S]sulphate in cartilage at the end of each experiment, in addition to that due to incorporated sulphate. The inorganic sulphate content of the serum was also determined as well as the distribution coefficient for the inorganic sulphate ion between cartilage and serum. From this information it was possible to calculate accurately the rate of sulphate uptake by cartilage in vivo and hence the turn-over rate. Experiments were then performed in vitro on cartilage from rabbits and dogs and the in vivo and in vitro results were compared. A very good agreement was obtained between the two sets of results. Studies were then carried out under exactly the same in vitro conditions on human articular cartilage and it was thus possible to obtain a turn-over rate for the latter which one could trust was close to the actual in vivo value. The mean half-lives thus obtained varied from 45 days for the young rabbit to 150 days for the adult dog and 800 days for the human femoral head. In human cartilage there were considerable variations in turn-over rate within a single joint as a function of depth below the surface, and between different joints. Thus, while the mean half-life for the human femoral head is 800 days, that for the femoral condyle is 300 days. Cartilage from osteoarthrosic femoral heads did not appear to differ much with respect to sulphate uptake from the normal specimens although the turn-over rates were somewhat higher.

[1]  D. M. Sherman,et al.  Biochemical and ultrastructural observations in normal and degenerative canine articular cartilage. , 1972, American journal of veterinary research.

[2]  D. Collins,et al.  Sulphate (35SO4) Fixation by Human Articular Cartilage compared in the Knee and Shoulder Joints , 1961, Annals of the rheumatic diseases.

[3]  A. Maroudas Distribution and diffusion of solutes in articular cartilage. , 1970, Biophysical journal.

[4]  H. Mankin,et al.  The turnover of adult rabbit articular cartilage. , 1969, The Journal of bone and joint surgery. American volume.

[5]  S. Lohmander,et al.  Chemical and metabolic heterogeneity of chondroitin sulfate and keratin sulfate in guinea pig cartilage and nucleus pulposus. , 1973, Biochimica et biophysica acta.

[6]  G. Meachim Sulphate Metabolism of Articular Cartilage after Surgical Interference with the Joint , 1964, Annals of the Rheumatic Diseases.

[7]  E. Davidson,et al.  Metabolism in vivo of connective-tissue mucopolysaccharides. I. Chondroitin sulfate C and keratosulfate of nucleus pulposus. , 1963, Biochimica et biophysica acta.

[8]  A. Maroudas,et al.  Transport of solutes through cartilage: permeability to large molecules. , 1976, Journal of anatomy.

[9]  T. Hardingham,et al.  Biosynthesis of proteoglycans in cartilage slices. Fractionation by gel chromatography and equilibrium density-gradient centrifugation. , 1972, The Biochemical journal.

[10]  J. Holmes,et al.  The use of radioisotopes to measure body fluid constituents. I. Plasma sulfate. , 1961, The Journal of laboratory and clinical medicine.

[11]  A. J. Bollet,et al.  Biochemical Findings in Normal and Osteoarthritic Articular Cartilage. II. Chondroitin Sulfate Concentration and Chain Length, Water, and Ash Content. , 1966, The Journal of clinical investigation.

[12]  H J Mankin,et al.  Biochemical and metabolic abnormalities in articular cartilage from osteo-arthritic human hips. , 1970, The Journal of bone and joint surgery. American volume.

[13]  J. A. Cifonelli,et al.  The metabolism of mucopolysaccharides in animals. III. Further studies on skin utilizing C14-glucose, C14-acetate, and S35-sodium sulfate. , 1956, The Journal of biological chemistry.

[14]  P. Bullough,et al.  Permeability of articular cartilage. , 1968, Nature.

[15]  D. Collins,et al.  Chondrocyte Function of Human Articular and Costal Cartilage Compared by Measuring the In Vitro Uptake of Labelled (35S) Sulphate , 1960, Annals of the rheumatic diseases.

[16]  A. Maroudas,et al.  Topographical Variation of Glycosaminoglycan Content in Normal and Fibrillated Tissue , 2022 .

[17]  A. Dorfman,et al.  Sodium chondroitin sulfate-protein complexes of cartilage. II. Metabolism. , 1960, The Journal of biological chemistry.

[18]  S. Gardell,et al.  DETERMINATION OF GLYCOSAMINOGLYCANS (MUCOPOLYSACCHARIDES) FROM TISSUE ON THE MICROGRAM SCALE. , 1964, Biochimica et biophysica acta.

[19]  A. Maroudas,et al.  Sulphate diffusion and incorporation into human articular cartilage , 1974 .

[20]  Stockwell Ra The interrelationship of cell density and cartilage thickness in mammalian articular cartilage. , 1971 .

[21]  D. Collins,et al.  Sulphate (35SO4) Uptake by Chondrocytes in Relation to Histological Changes in Osteo-Arthritic Human Articular Cartilage , 1960, Annals of the rheumatic diseases.