MMP-13 is induced during chondrocyte hypertrophy
Document Type
Article
Publication Date
2000
Abstract
During development, mRNA for matrix metalloproteinase-13 (MMP-13) is found associated with cartilage undergoing hypertrophy, suggesting that this collagenase plays a role in cell enlargement and/or cartilage calcification. Using chondrocytes from prehypertrophic cartilage of chick embryo sternae, we have examined the relationship between MMP-13 expression and the transition to hypertrophy. When hypertrophy was induced by serum-free culture with ascorbate and bone morphogenetic protein-2 (BMP-2), MMP-13 mRNA levels paralleled those for type X collagen. Chondrocytes from the caudal, nonhypertrophying portion of chick sternae expressed neither type X collagen nor MMP-13, confirming that MMP-13 mRNA is a marker for hypertrophy. Zymography with conditioned medium yielded a proteinase band at 59 kDa, which was absent in nonhypertrophic chondrocytes. A polyclonal antibody raised against chick MMP-13 reacted with the 59-kDa protein, confirming that it is MMP-13. Although mRNA for MMP-13 peaked at days 4-5 of culture, only low levels of MMP-13 activity were present, and the activity increased gradually in parallel with later increases in MMP-2. These results suggest that MMP-13 is activated by MMP-2 during chondrocyte maturation, and that the combination of both proteinases is required to prepare cartilage matrix for subsequent calcification, before endochondral ossification. (C) 2000 Wiley-Liss, Inc.
Publication Title
Journal of cellular biochemistry
Volume
77
Issue
4
First Page
678
Last Page
693
Recommended Citation
D'Angelo, Marina; Yan, Z.; Nooreyazdan, M.; Pacifici, Maurizio; Sarment, D. S.; Billings, Paul C.; and Leboy, Phoebe S., "MMP-13 is induced during chondrocyte hypertrophy" (2000). PCOM Scholarly Works. 362.
https://digitalcommons.pcom.edu/scholarly_papers/362
Comments
This article was published in Journal of cellular biochemistry, Volume 77, Issue 4, Pages 678-693.
The published version is available at http://dx.doi.org/10.1002/(SICI)1097-4644(20000615)77:4<678::AID-JCB15>3.0.CO;2-P.Copyright © 2000 Wiley.