Severe destruction of articular cartilage in osteoarthritis manifests
clinically when repair processes cannot keep up with the catabolic pro
cesses. Loss of proteoglycans, which give the tissue its ability to un
dergo reversible deformation, precedes and probably contributes signif
icantly to breakdown of the matrix in the most superficial layers of a
rticular cartilage. In this study, we have examined the ability of dit
hio-bis[succinimidyl proprionate], a bifunctional reagent with a 1.2-n
m span that cross-links proteins at lysine amino acid, and poly-L-lysi
ne of high molecular weight (average MW 360,000) to reduce passive los
s of proteoglycans and collagen from thin slices (40 and 200 mu m) of
bovine nasal and human patellar cartilage incubated for 7 days in buff
er at 4 degrees C. We present evidence that treatment of thin slices o
f cartilage with either of these agents is effective in reducing the l
oss of proteoglycans and collagen from the cartilage matrix and we def
ine conditions (length of treatment and concentrations required) under
which the stabilization of the cartilage matrix is optimized. Chemica
l stabilization of cartilage matrix may become an important modality o
f treatment in osteoarthritis by protecting the environment around cho
ndrocytes during the repair process. (C) 1994 Academic Press, Inc.