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

被引:728
作者
Stanton, H
Rogerson, FM
East, CJ
Golub, SB
Lawlor, KE
Meeker, CT
Little, CB
Last, K
Farmer, PJ
Campbell, IK
Fourie, AM
Fosang, AJ [1 ]
机构
[1] Univ Melbourne, Dept Paediat, Parkville, Vic 3052, Australia
[2] Royal Childrens Hosp, Murdoch Childrens Res Inst, Dept Surg, Parkville, Vic 3052, Australia
[3] Univ Sydney, Royal N Shore Hosp, Raymond Purves Bone & Joint Res Labs, St Leonards, NSW 2065, Australia
[4] Walter & Eliza Hall Inst Med Res, Reid Rheumatol Lab, Parkville, Vic 3052, Australia
[5] Johnson & Johnson Pharmaceut Res & Dev, San Diego, CA 92121 USA
基金
英国医学研究理事会;
关键词
D O I
10.1038/nature03417
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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(1)) family of proteinases. ADAMTS1, 8 and 9 have weak aggrecan-degrading activity(2-5). However, they are not thought to be the primary aggrecanases because ADAMTS1 null mice are not protected from experimental arthritis(6), and cleavage by ADAMTS8 and 9 is highly inefficient. Although ADAMTS4 and 5 are expressed in joint tissues(7-13), 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.
引用
收藏
页码:648 / 652
页数:5
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