Matrix metalloproteinases and their clinical applications in orthopaedics

被引:86
作者
Bramono, DS
Richmond, JC
Weitzel, PP
Kaplan, DL
Altman, GH
机构
[1] Tufts Univ, Dept Biomed Engn, Medford, MA 02155 USA
[2] New England Baptist Hosp, Dept Orthopaed Surg, Boston, MA USA
[3] Tufts Univ New England Med Ctr, Dept Orthopaed, Boston, MA 02111 USA
关键词
D O I
10.1097/01.blo.0000144166.66737.3a
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Imbalance in the expression of matrix metalloproteinases and their inhibitors contribute considerably to abnormal connective tissue degradation prevalent in various orthopaedic joint diseases such as rheumatoid arthritis and osteoarthritis. Matrix metalloproteinase expression has been detected in ligament, tendon, and cartilage tissues in the joint. They are known to contribute to the development, remodeling, and maintenance of healthy tissue through their ability to cleave a wide range of extracellular matrix substrates. Their role has been extended to cell growth, migration, differentiation, and apoptosis. In orthopaedics, their clinical applications constantly are being explored. The multiple steps in matrix metalloproteinase regulation offer potential targets for inhibition, useful in drug therapy. The correlation between matrix metalloproteinases and progression in joint erosion presents potential prognostic and diagnostic tools in rheumatoid arthritis. Matrix metalloproteinases also can be incorporated into scaffold design to control the degradation rate of engineered tissue constructs. This current review aims to summarize and emphasize the importance of matrix metalloproteinases and their natural inhibitors in the maturation of musculoskeletal tissue through matrix remodeling and, therefore, in the generation of a new clinical potential in orthopaedics.
引用
收藏
页码:272 / 285
页数:14
相关论文
共 117 条
[1]   Expression of matrix metalloproteinase 9 (96-kd gelatinase B) in human rheumatoid arthritis [J].
Ahrens, D ;
Koch, AE ;
Pope, RM ;
SteinPicarella, M ;
Niedbala, MJ .
ARTHRITIS AND RHEUMATISM, 1996, 39 (09) :1576-1587
[2]  
Aigner T, 2001, ARTHRITIS RHEUM-US, V44, P2777, DOI 10.1002/1529-0131(200112)44:12<2777::AID-ART465>3.0.CO
[3]  
2-H
[4]   Rabbit tendon cells produce MMP-3 in response to fluid flow without significant calcium transients [J].
Archambault, JM ;
Elfervig-Wall, MK ;
Tsuzaki, M ;
Herzog, W ;
Banes, AJ .
JOURNAL OF BIOMECHANICS, 2002, 35 (03) :303-309
[5]   Molecular cloning and mRNA tissue distribution of a novel matrix metalloproteinase isolated from porcine enamel organ [J].
Bartlett, JD ;
Simmer, JP ;
Xue, J ;
Margolis, HC ;
Moreno, EC .
GENE, 1996, 183 (1-2) :123-128
[6]   Relative messenger RNA expression profiling of collagenases and aggrecanases in human articular chondrocytes in vivo and in vitro [J].
Bau, B ;
Gebhard, PM ;
Haag, J ;
Knorr, T ;
Bartnik, E ;
Aigner, T .
ARTHRITIS AND RHEUMATISM, 2002, 46 (10) :2648-2657
[7]   The AP-1 site and MMP gene regulation: What is all the fuss about? [J].
Benbow, U ;
Brinckerhoff, CE .
MATRIX BIOLOGY, 1997, 15 (8-9) :519-526
[8]  
Berton A., 2000, Molecular Cell Biology Research Communications, V3, P173, DOI 10.1006/mcbr.2000.0210
[9]   Up-regulation of matrix metalloproteinase expression and activation following cyclical compressive loading of articular cartilage in vitro [J].
Blain, EJ ;
Gilbert, SJ ;
Wardale, RJ ;
Capper, SJ ;
Mason, DJ ;
Duance, VC .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2001, 396 (01) :49-55
[10]   Matrix metalloproteinase-1,-3,-13 and aggrecanase-1 and-2 are differentially expressed in experimental osteoarthritis [J].
Bluteau, G ;
Conrozier, T ;
Mathieu, P ;
Vignon, E ;
Herbage, D ;
Mallein-Gerin, F .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2001, 1526 (02) :147-158