Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

The loss of extracellular matrix macromolecules from the cartilage results in serious impairment of joint function. Metalloproteinases called 'aggrecanases' that cleave the Glu373-Ala374 bond of the aggrecan core protein play a key role in the early stages of cartilage destruction in rheumatoid arthritis and in osteoarthritis. Three members of the ADAMTS family of proteinases, ADAMTS-1, ADAMTS-4 and ADAMTS-5, have been identified as aggrecanases. Matrix metalloproteinases, which are also found in arthritic joints, cleave aggrecans, but at a distinct site from the aggrecanases (i.e. Asn341-Phe342). The present review discuss the enzymatic properties of the three known aggrecanases, the regulation of their activities, and their role in cartilage matrix breakdown during the development of arthritis in relation to the action of matrix metalloproteinases.

Type

Journal article

Journal

Arthritis res ther

Publication Date

2003

Volume

5

Pages

94 - 103

Keywords

ADAM Proteins, ADAMTS1 Protein, ADAMTS4 Protein, ADAMTS5 Protein, Cartilage, Disintegrins, Endopeptidases, Extracellular Matrix, Humans, Matrix Metalloproteinases, Metalloendopeptidases, Procollagen N-Endopeptidase, Protein Processing, Post-Translational, Tissue Inhibitor of Metalloproteinase-3