Matrix metalloproteinases are involved in C-terminal and interglobular domain processing of cartilage aggrecan in late stage cartilage degradation

被引:142
作者
Little, CB
Hughes, CE
Curtis, CL
Janusz, MJ
Bohne, R
Wang-Weigand, S
Taiwo, YO
Mitchell, PG
Otterness, IG
Flannery, CR
Caterson, B
机构
[1] Univ Wales Coll Cardiff, Cardiff Sch Biosci, Connect Tissue Biol Lab, Cardiff CF10 3US, S Glam, Wales
[2] Procter & Gamble Pharmaceut, Hlth Care Res Ctr, Mason, OH 45040 USA
[3] Pfizer Inc, Dept Canc Immunol & Infect Dis, Groton, CT 06340 USA
[4] Genet Inst Inc, Cambridge, MA 02140 USA
[5] Univ Melbourne, Dept Paediat, Cell & Matrix Biol Res Unit, Parkville, Vic 3052, Australia
[6] Royal Childrens Hosp, Murdoch Childrens Res Inst, Parkville, Vic 3052, Australia
基金
英国惠康基金;
关键词
matrix metalloproteinases; aggrecanase; cartilage catabolism;
D O I
10.1016/S0945-053X(02)00004-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Monoclonal antibody (MAb) technology was used to examine aggrecan metabolites and the role of aggrecanases and matrix metalloproteinases (MMPs) in proteolysis of the interglobular domain (IGD) and C-terminus of aggrecan. An in vitro model of progressive cartilage degradation characterized by early proteoglycan loss and late stage collagen catabolism was evaluated in conjunction with a broad-spectrum inhibitor of MMPs. We have for the first time demonstrated that IGD cleavage by MMPs occurs during this late stage cartilage degeneration, both as a primary event in association with glycosaminoglycan (GAG) release from the tissue and secondarily in trimming of aggrecanase-generated G1 metabolites. Additionally, we have shown that MMPs were responsible for C-terminal catabolism of aggrecan and generation of chondroitin sulfate (CS) deficient aggrecan monomers and that this aggrecan truncation occurred prior to detectable IGD cleavage by MMPs. The onset of this later stage MMP activity was also evident by the generation of MMP-specific link protein catabolites in this model culture system. Recombinant MMP-1, -3 and -13 were all capable of C-terminally truncating aggrecan with at least two cleavage sites N-terminal to the CS attachment domains of aggrecan. Through analysis of aggrecan metabolites in pathological synovial fluids from human, canine and equine sources, we have demonstrated the presence of aggrecan catabolites that appear to have resulted from similar C-terminal processing of aggrecan as that induced in our in vitro culture systems. Finally, by developing a new MAb recognizing a linear epitope in the IGD of aggrecan, we have identified two novel aggrecan metabolites generated by an as yet unidentified proteolytic event. Collectively, these results suggest that C-terminal processing of aggrecan by MMPs may contribute to the depletion of cartilage GAG that leads to loss of tissue function in aging and disease. Furthermore, analysis of aggrecan metabolites resulting from both C-terminal and IGD cleavage by MMPs may prove useful in monitoring different stages in the progression of cartilage degeneration. (C) 2002 Elsevier Science B.V. and International Society of Matrix Biology. All rights reserved.
引用
收藏
页码:271 / 288
页数:18
相关论文
共 74 条
[1]
Cloning and characterization of ADAMTS11, an aggrecanase from the ADAMTS family [J].
Abbaszade, I ;
Liu, RQ ;
Yang, F ;
Rosenfeld, SA ;
Ross, OH ;
Link, JR ;
Ellis, DM ;
Tortorella, MD ;
Pratta, MA ;
Hollis, JM ;
Wynn, R ;
Duke, JL ;
George, HJ ;
Hillman, MC ;
Murphy, K ;
Wiswall, BH ;
Copeland, RA ;
Decicco, CP ;
Bruckner, R ;
Nagase, H ;
Itoh, Y ;
Newton, RC ;
Magolda, RL ;
Trzaskos, JM ;
Hollis, GF ;
Arner, EC ;
Burn, TC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (33) :23443-23450
[2]
[Anonymous], BIOL SYNOVIAL JOINT
[3]
Cytokine-induced cartilage proteoglycan degradation is mediated by aggrecanase [J].
Arner, EC ;
Hughes, CE ;
Decicco, CP ;
Caterson, B ;
Tortorella, MD .
OSTEOARTHRITIS AND CARTILAGE, 1998, 6 (03) :214-228
[4]
Generation and characterization of aggrecanase - A soluble, cartilage-derived aggrecan-degrading activity [J].
Arner, EC ;
Pratta, MA ;
Trzaskos, JM ;
Decicco, CP ;
Tortorella, MD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (10) :6594-6601
[5]
BAKER JR, 1979, J BIOL CHEM, V254, P2387
[6]
USE OF AN ANTIBODY AGAINST THE MATRIX METALLOPROTEINASE-GENERATED AGGRECAN NEOEPITOPE FVDIPEN-COOH TO ASSESS THE EFFECTS OF STROMELYSIN IN A RABBIT MODEL OF CARTILAGE DEGRADATION [J].
BAYNE, EK ;
MACNAUL, KL ;
DONATELLI, SA ;
CHRISTEN, A ;
GRIFFIN, PR ;
HOERRNER, LA ;
CALAYCAY, JR ;
AYALA, JM ;
CHAPMAN, K ;
HAGMANN, W ;
WEIDNER, JR ;
MCDONNELL, J ;
MOORE, VL ;
MUMFORD, RA ;
LARK, MW ;
HUTCHINSON, NI .
ARTHRITIS AND RHEUMATISM, 1995, 38 (10) :1400-1409
[7]
Enhanced cleavage of type II collagen by collagenases in osteoarthritic articular cartilage [J].
Billinghurst, RC ;
Dahlberg, L ;
Ionescu, M ;
Reiner, A ;
Bourne, R ;
Rorabeck, C ;
Mitchell, P ;
Hambor, J ;
Diekmann, O ;
Tschesche, H ;
Chen, J ;
VanWart, H ;
Poole, AR .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (07) :1534-1545
[8]
Nitric oxide inhibits aggrecan degradation in explant cultures of equine articular cartilage [J].
Bird, JLE ;
May, S ;
Bayliss, MT .
EQUINE VETERINARY JOURNAL, 2000, 32 (02) :133-139
[9]
PASSIVE LOSS OF PROTEOGLYCAN FROM ARTICULAR-CARTILAGE EXPLANTS [J].
BOLIS, S ;
HANDLEY, CJ ;
COMPER, WD .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 993 (2-3) :157-167
[10]
Inhibition of bovine nasal cartilage degradation by selective matrix metalloproteinase inhibitors [J].
Bottomley, KM ;
Borkakoti, N ;
Bradshaw, D ;
Brown, PA ;
Broadhurst, MJ ;
Budd, JM ;
Elliott, L ;
Eyers, P ;
Hallam, TJ ;
Handa, BK ;
Hill, CH ;
James, M ;
Lahm, HW ;
Lawton, G ;
Merritt, JE ;
Nixon, JS ;
Rothlisberger, U ;
Whittle, A ;
Johnson, WH .
BIOCHEMICAL JOURNAL, 1997, 323 :483-488