Cysteine proteinases, cathepsins B, H, K, L and S, have been implicated in
several proteolytic processes during development, growth, remodeling and ag
ing, as well as in a variety of pathological processes. For systematic anal
ysis of cathepsin gene expression we have produced cDNA clones for mouse an
d human cysteine cathepsins. Northern analysis of a panel of total RNAs iso
lated from 16-19 different human and mouse tissues revealed the presence of
mRNAs for cathepsin B, H, K, L and S in most tissues, but each with a dist
inct profile. Of the different cathepsin mRNAs, those for cathepsin K were
clearly the highest in bone and cartilage. However, relatively high mRNA le
vels for the other cathepsins were also present in these tissues. To better
understand the roles of different cathepsins during endochondral ossificat
ion in mouse long bones, cathepsin mRNAs were localized by in situ hybridiz
ation. Cathepsin K mRNAs were predominantly seen in multinucleated chondroc
lastic and osteoclastic cells at the osteochondral junction and on the surf
ace of bone spicules. The other cathepsin mRNAs were also seen in osteoclas
ts, and in hypertrophic and proliferating chondrocytes. These observations
were confirmed by immunohistochemistry and suggest that all cysteine cathep
sins are involved in matrix degradation during endochondral ossification. (
C) 1999 Elsevier Science B.V. All rights reserved.