Mechanical and physicochemical regulation of the action of insulin-like growth factor-I on articular cartilage

The development and maintenance of healthy joints is a complex process invo lving many physical and biological stimuli. This study investigates the int eraction between insulin-like growth factor-I (IGF-I) and static mechanical compression in the regulation of articular cartilage metabolism. Bovine ca rtilage explants were treated with concentrations of IGF-I from 0 to 300 ng /ml in the presence or absence of 0-50% static compression, and the transie nt and steady-state incorporation of [H-3]proline and [S-35]sulfate into ma trix components were measured. In parallel studies, cartilage explants were treated with 0-300 ng/ml IGF-I at media pH ranging from 6.4 to 7.2 and the steady-state incorporation of [H-3]proline and [S-35]sulfate was measured. The effect of 50% static compression on IGF-I transport was determined by measuring the uptake of I-125-labeled IGF-I into cartilage explants, Static compression decreased both [H-3]proline and [S-35]sulfate incorporation in a dose-dependent manner in the presence or absence of IGF-I. IGF-I increas ed [H-3]proline and [S-35]sulfate incorporation in a dose-dependent manner in the presence or absence of compression, but the anabolic effect of the g rowth factor was lessened when the tissue was compressed by 50%. The respon se of cartilage explants to IGF-I was similarly lessened in unstrained tiss ue cultured in media at pH 6.4, a condition which results in a similar intr atissue pH to that when cartilage is compressed by 50%. The characteristic time constant (tau) for IGF-I stimulation of cartilage explants was approxi mately 24 h, while tau for inhibition of biosynthesis by static compression was approximately 2 h, Samples which mere both com-pressed and treated wit h IGF-I demonstrated an initial decrease in biosynthetic activity at 2 h, f ollowed by an increase at 24 h, Static compression did not alter tau for [I -125]labeled IGF-I transport into cartilage but decreased the concentration of I-125-labeled IGF-I in the tissue at equilibrium. (C) 2000 Academic Pre ss.