Journal
CALCIFIED TISSUE INTERNATIONAL
Volume 91, Issue 1, Pages 32-39Publisher
SPRINGER
DOI: 10.1007/s00223-012-9604-7
Keywords
Cathepsin K; Type I collagen posttranslational modification; Bone matrix solubilization
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Bone collagen undergoes a series of enzymatic and nonenzymatic posttranslational modifications with maturation. The aim of this study was to analyze the collagenolytic efficiency of cathepsin K in relation to the extent of bone collagen age. Bone collagen posttranslational maturation was induced in vitro by preincubating bovine fetal cortical bone specimens at 37 A degrees C for different times. The collagen enzymatic cross-links pyridinoline (PYD) and deoxypyridinoline (DPD), the advanced glycation end product pentosidine (PEN), and the native (alpha) and beta-isomerized C-telopeptide (CTX) isomers were measured in each bone specimen. After extraction, bone collagen was incubated with human recombinant cathepsin K at different concentrations and its collagenolytic activity was measured by the release of hydroxyproline. To assess the affinity of cathepsin K for isomerized and nonisomerized CTX isomers, incubation with cathepsin K was also performed in the presence of various concentrations of a specific inhibitor. We showed that preincubation of bone collagen at 37 A degrees C induces a marked increase in the bone concentration of PYD, DPD, and PEN and of CTX isomerization as reflected by the ratio of alpha-/beta CTX. This increase was associated with a parallel increase in the efficiency of cathepsin K to solubilize bone collagen. When cathepsin K was incubated in the presence of an inhibitor, the beta-isomerized form of collagen from 3-month- and 8-year-old bovine bone was more susceptible to degradation than the native alpha form. These results suggest that the collagenolytic activity of cathepsin K may be increased toward more matured bone collagen.
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