Proteases involved in cartilage matrix degradation in osteoarthritis

被引:442
作者
Troeberg, Linda [1 ]
Nagase, Hideaki [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Kennedy Inst, Div Rheumatol, London W6 8LH, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2012年 / 1824卷 / 01期
关键词
Osteoarthritis; Proteinase; Cartilage; Aggrecanase; Collagenase; HUMAN ARTICULAR-CARTILAGE; DISCOIDIN-DOMAIN RECEPTOR-2; HUMAN SYNOVIAL-FLUID; GROWTH-FACTOR; CATHEPSIN-K; IN-VIVO; AGGRECAN DEGRADATION; SERINE-PROTEASE; II COLLAGEN; ADAMTS4; AGGRECANASE-1;
D O I
10.1016/j.bbapap.2011.06.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Osteoarthritis is a common joint disease for which there are currently no disease-modifying drugs available. Degradation of the cartilage extracellular matrix is a central feature of the disease and is widely thought to be mediated by proteinases that degrade structural components of the matrix, primarily aggrecan and collagen. Studies on transgenic mice have confirmed the central role of Adamalysin with Thrombospondin Motifs 5 (ADAMTS-5) in aggrecan degradation, and the collagenolytic matrix metalloproteinase MMP-13 in collagen degradation. This review discusses recent advances in current understanding of the mechanisms regulating expression of these key enzymes, as well as reviewing the roles of other proteinases in cartilage destruction. This article is part of a Special Issue entitled: Proteolysis 50 years after the discovery of lysosome. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:133 / 145
页数:13
相关论文
共 245 条
  • [51] Histone deacetylase inhibitors repress the transactivation potential of hypoxia-inducible factors independently of direct acetylation of HIF-α
    Fath, DM
    Kong, XG
    Liang, DM
    Lin, Z
    Chou, A
    Jiang, YB
    Fang, J
    Caro, J
    Sang, NL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (19) : 13612 - 13619
  • [52] Role of cytokines in rheumatoid arthritis: an education in pathophysiology and therapeutics
    Feldmann, Marc
    Maini, Ravinder N.
    [J]. IMMUNOLOGICAL REVIEWS, 2008, 223 : 7 - 19
  • [53] CAPACITY OF PIG ARTICULAR-CARTILAGE IN ORGAN-CULTURE TO REGENERATE AFTER BREAKDOWN INDUCED BY COMPLEMENT-SUFFICIENT ANTISERUM TO PIG ERYTHROCYTES
    FELL, HB
    BARRATT, MEJ
    WELLAND, H
    GREEN, R
    POOLE, AR
    [J]. CALCIFIED TISSUE RESEARCH, 1976, 20 (01): : 3 - 21
  • [54] Developments in the clinical understanding of osteoarthritis
    Felson, David T.
    [J]. ARTHRITIS RESEARCH & THERAPY, 2009, 11 (01)
  • [55] Protease-activated receptor 2: a novel pathogenic pathway in a murine model of osteoarthritis
    Ferrell, William R.
    Kelso, Elizabeth B.
    Lockhart, John C.
    Plevin, Robin
    McInnes, Iain B.
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2010, 69 (11) : 2051 - 2054
  • [56] Autocatalytic cleavage of ADAMTS-4 (Aggrecanase-1) reveals multiple glycosaminoglycan-binding sites
    Flannery, CR
    Zeng, WL
    Corcoran, C
    Collins-Racie, LA
    Chockalingam, PS
    Hebert, T
    Mackie, SA
    McDonagh, T
    Crawford, TK
    Tomkinson, KN
    LaVallie, ER
    Morris, EA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (45) : 42775 - 42780
  • [57] FOSANG AJ, 1991, J BIOL CHEM, V266, P15579
  • [58] FOSANG AJ, 1992, J BIOL CHEM, V267, P19470
  • [59] FIBROBLAST AND NEUTROPHIL COLLAGENASES CLEAVE AT 2 SITES IN THE CARTILAGE AGGRECAN INTERGLOBULAR DOMAIN
    FOSANG, AJ
    LAST, K
    KNAUPER, V
    NEAME, PJ
    MURPHY, G
    HARDINGHAM, TE
    TSCHESCHE, H
    HAMILTON, JA
    [J]. BIOCHEMICAL JOURNAL, 1993, 295 : 273 - 276
  • [60] Degradation of cartilage aggrecan by collagenase-3 (MMP-13)
    Fosang, AJ
    Last, K
    Knauper, V
    Murphy, G
    Neame, PJ
    [J]. FEBS LETTERS, 1996, 380 (1-2) : 17 - 20