The breakdown of aggrecan in cartilage is, in part, mediated by an enzyme named aggrecanase that cleaves within the interglobular domain of the molecule between a glutamic residue and an alanine residue. Although the enzyme cleavage site has been identified, the identity, characteristics and localization of this enzyme remain unclear. We have demonstrated that membranes isolated from stimulated chondrocytes are able to generate aggrecan fragments that are labelled by an antibody that recognizes the new N-terminus formed by aggrecanase activity. It was further shown that the membrane activity was a metalloproteinase but was not inhibited by the naturally occurring matrix metalloproteinase (MMP) inhibitors, TIMPs 1 and 2. These results show that an aggrecanase activity is associated with the membranes of the chondrocytes and is a metalloproteinase, but might not be a member of the MMP family.
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November 1998
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Research Article|
November 15 1998
An aggrecan-degrading activity associated with chondrocyte membranes
Caron J. BILLINGTON;
Caron J. BILLINGTON
*Department of Rheumatology, School of Clinical and Medical Sciences, University of Newcastle, Newcastle upon Tyne NE2 4HH, U.K.
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Ian M. CLARK;
Ian M. CLARK
†Department of Biological Sciences, University of East Anglia, Norwich NR4 7TJ, U.K.
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Tim E. CAWSTON
Tim E. CAWSTON
1
*Department of Rheumatology, School of Clinical and Medical Sciences, University of Newcastle, Newcastle upon Tyne NE2 4HH, U.K.
1To whom correspondence should be addressed (e-mail [email protected]).
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Publisher: Portland Press Ltd
Received:
May 26 1998
Revision Received:
August 19 1998
Accepted:
September 17 1998
Online ISSN: 1470-8728
Print ISSN: 0264-6021
The Biochemical Society, London © 1998
1998
Biochem J (1998) 336 (1): 207–212.
Article history
Received:
May 26 1998
Revision Received:
August 19 1998
Accepted:
September 17 1998
Citation
Caron J. BILLINGTON, Ian M. CLARK, Tim E. CAWSTON; An aggrecan-degrading activity associated with chondrocyte membranes. Biochem J 15 November 1998; 336 (1): 207–212. doi: https://doi.org/10.1042/bj3360207
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