Inhibition of ADAMTS4 (aggrecanase‐1) by tissue inhibitors of metalloproteinases (TIMP‐1, 2, 3 and 4)
Open Access
- 10 April 2001
- journal article
- Published by Wiley in FEBS Letters
- Vol. 494 (3) , 192-195
- https://doi.org/10.1016/s0014-5793(01)02323-7
Abstract
ADAMTS4 (aggrecanase‐1) is considered to play a key role in the degradation of aggrecan in arthritides. The inhibitory activity of tissue inhibitors of metalloproteinases (TIMPs) to ADAMTS4 was examined in an assay using aggrecan substrate. Among the four TIMPs, TIMP‐3 inhibited the activity most efficiently with an IC50 value of 7.9 nM, which was at least 44‐fold lower than that of TIMP‐1 (350 nM) and TIMP‐2 (420 nM) and >250‐fold less than that of TIMP‐4 (2 μM for 35% inhibition). These results suggest that TIMP‐3 is a potent inhibitor against the aggrecanase activity of ADAMTS4 in vivo.Keywords
This publication has 25 references indexed in Scilit:
- Brevican Is Degraded by Matrix Metalloproteinases and Aggrecanase-1 (ADAMTS4) at Different SitesJournal of Biological Chemistry, 2000
- ADAM 12-S Cleaves IGFBP-3 and IGFBP-5 and Is Inhibited by TIMP-3Biochemical and Biophysical Research Communications, 2000
- Generation and Novel Distribution of Matrix Metalloproteinase-derived Aggrecan Fragments in Porcine Cartilage ExplantsJournal of Biological Chemistry, 2000
- Expression of ADAMTS Homologues in Articular CartilageBiochemical and Biophysical Research Communications, 1999
- Generation and Characterization of AggrecanaseJournal of Biological Chemistry, 1999
- An Essential Role for Ectodomain Shedding in Mammalian DevelopmentScience, 1998
- TNF‐α converting enzyme (TACE) is inhibited by TIMP‐3FEBS Letters, 1998
- A metalloproteinase disintegrin that releases tumour-necrosis factor-α from cellsNature, 1997
- Aggrecan is degraded by matrix metalloproteinases in human arthritis. Evidence that matrix metalloproteinase and aggrecanase activities can be independent.Journal of Clinical Investigation, 1996
- A metalloprotease-disintegrin participating in myoblast fusionNature, 1995