Journal
OSTEOARTHRITIS AND CARTILAGE
Volume 19, Issue 11, Pages 1356-1362Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.joca.2011.07.019
Keywords
Cartilage boundary lubrication; Hyaluronan; Proteoglycan 4 (PRG4)
Categories
Funding
- Natural Sciences & Engineering Research Council of Canada
- Canadian Arthritis Network
- Faculty of Kinesiology
- Schulich School of Engineering's Centre for Bioengineering Research and Education at the University of Calgary
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Objectives: (1) assess the molecular weight dependence of hyaluronan's (HA) cartilage boundary lubricating ability, alone and in combination with proteoglycan 4 (PRG4), at physiological concentrations; (2) determine if HA and PRG4 interact in solution via electrophoretic mobility shift assay (EMSA). Methods: The cartilage boundary lubricating ability of a broad range of MW HA (20 kDa, 132 kDa, 780 kDa, 1.5 MDa, and 5 MDa) at 3.33 mg/ml, both alone and in combination with PRG4 at 450 mu g/ml, was assessed using a previously described cartilage-on-cartilage friction test. Static, mu(static,) (Neq,) and kinetic, , were calculated. An EMSA was conducted with PRG4 and monodisperse 150 kDa and 1,000 kDa HA. Results: Friction coefficients were reduced by HA, in a MW-dependent manner. Values of in 20 kDa HA, 0.098 (0.089, 0.108), were significantly greater compared to both 780 kDa, 0.080 (0.072, 0.088), and 5 MDa, 0.079 (0.070, 0.089). Linear regression showed a significant correlation between both mu(static,) (Neq) and , and log HA MW. Friction coefficients were also reduced by PRG4, and with subsequent addition of HA; however the synergistic effect was not dependent on HA MW. Values of Neq> in PRG4, 0.080 (0.047, 0.113), were significantly greater than values of PRG4 + various MW HA (similar in value, averaging 0.040 (0.033, 0.047)). EMSA indicated that migration of 150 kDa and 1,000 kDa HA was retarded when combined with PRG4 at high PRG4:HA ratios. Conclusions: These results suggest alterations in HA MW could significantly affect synovial fluid's cartilage boundary lubricating ability, yet this diminishment in function could be circumvented by physiological levels of PRG4 forming a complex, potentially in solution, with HA. (C) 2011 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
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