ADAMTS5 is the major aggrecanase in mouse cartilage in vivo and in vitro

• Published in: Nature 2005-03, Vol.434 (7033), p.648-652
• Main Authors: Golub, Suzanne B, Rogerson, Fraser M, Campbell, Ian K, East, Charlotte J, Lawlor, Kate E, Little, Christopher B, Fourie, Anne M, Fosang, Amanda J, Meeker, Clare T, Last, Karena, Stanton, Heather, Farmer, Pamela J
• Format: Article
• Language: English
• Subjects: ADAM Proteins; ADAMTS4 Protein; ADAMTS5 Protein; Aggrecans; Animals; Antigens - immunology; Arthritis; Arthritis - enzymology; Arthritis - genetics; Arthritis - immunology; Arthritis - metabolism; Biological and medical sciences; Cartilage; Cartilage - drug effects; Cartilage - enzymology; Cartilage - metabolism; Disease; Disease Models, Animal; Diseases of the osteoarticular system; Drug therapy; Endopeptidases - deficiency; Endopeptidases - genetics; Endopeptidases - metabolism; Enzymes; Extracellular Matrix Proteins - metabolism; Extracellular Matrix Proteins - secretion; Genotype; Humanities and Social Sciences; Interleukin-1 - pharmacology; Lectins, C-Type; letter; Medical sciences; Metalloendopeptidases - deficiency; Metalloendopeptidases - genetics; Metalloendopeptidases - metabolism; Mice; Mice, Knockout; multidisciplinary; Osteoarthritis; Procollagen N-Endopeptidase - genetics; Procollagen N-Endopeptidase - metabolism; Proteoglycans - metabolism; Proteoglycans - secretion; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - genetics; RNA, Messenger - metabolism; Rodents; Science; Science (multidisciplinary); Tissue Culture Techniques
• ISSN: 0028-0836; 1476-4687
• DOI: 10.1038/nature03417

Aggrecan is the major proteoglycan in cartilage, endowing this tissue with the unique capacity to bear load and resist compression. In arthritic cartilage, aggrecan is degraded by one or more 'aggrecanases' from the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) family of proteinases. ADAMTS1, 8 and 9 have weak aggrecan-degrading activity. However, they are not thought to be the primary aggrecanases because ADAMTS1 null mice are not protected from experimental arthritis, and cleavage by ADAMTS8 and 9 is highly inefficient. Although ADAMTS4 and 5 are expressed in joint tissues, and are known to be efficient aggrecanases in vitro, the exact contribution of these two enzymes to cartilage pathology is unknown. Here we show that ADAMTS5 is the major aggrecanase in mouse cartilage, both in vitro and in a mouse model of inflammatory arthritis. Our data suggest that ADAMTS5 may be a suitable target for the development of new drugs designed to inhibit cartilage destruction in arthritis, although further work will be required to determine whether ADAMTS5 is also the major aggrecanase in human arthritis.