Neutrophil collagenase (MMP-8) cleaves at the aggrecanase site E373–A374 in the interglobular domain of cartilage aggrecan

Author:

Fosang A J1,Last K1,Neame P J2,Murphy G3,Knäuper V24,Tschesche H4,Hughes C E5,Caterson B5,Hardingham T E6

Affiliation:

1. University of Melbourne, Department of Medicine, Royal Melbourne Hospital, Parkville, 3050, Australia

2. Shriners Hospital for Crippled Children, Tampa, Florida 33612, U.S.A

3. Strangeways Research Laboratory, Cambridge CB1 4RN, U.K.

4. Universitat Bielefeld, Fakultat fur Chemie, Lehrstuhl fur Biochemie, W-4800 Bielefeld, Germany

5. Universiy of north carolina Department of orthopaedics, chapel Hill, NC, USA

6. kennedy institute of Rheumatology, Hammersmith, london W6 7DW, UK

Abstract

Native and recombinant neutrophil collagenase (MMP-8) was shown to cleave at the E373-A374 ‘aggrecanase’ site in the interglobular domain of aggrecan. The time course of digestion in vitro showed that MMP-8 cleaved initially at N341-F342, the predominant metalloproteinase site, before cleaving at the E373-A374 site. A synthetic peptide, IPENFFG, inhibited cleavage at E373-A374 but not N341-F342 in vitro, indicating that the E373-A374 sequence was a less preferred site for MMP-8 cleavage than N341-F342. IPENFFG also inhibited release of A374 RGSVI fragments from cartilage in explant culture, suggesting that a metalloproteinase cleaved at the aggrecanase site in situ. The possibility remains that ‘aggrecanase’ may be a metalloproteinase in cartilage.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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