Cartilage in normal and osteoarthritis conditions

被引:431
作者
Martel-Pelletier, Johanne [1 ]
Boileau, Christelle
Pelletier, Jean-Pierre
Roughley, Peter J. [2 ]
机构
[1] Univ Montreal, Ctr Hosp, Notre Dame Hosp, Osteoarthritis Res Unit, Montreal, PQ H2L 4M1, Canada
[2] Shriners Hosp Children, Genet Unit, Montreal, PQ, Canada
来源
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY | 2008年 / 22卷 / 02期
关键词
anabolic; non-anabolic; and catabolic growth factors; biological markers; cartilage; collagens; cytokines; osteoarthritis; proteases; proteoglycans;
D O I
10.1016/j.berh.2008.02.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The preservation of articular cartilage depends on keeping the cartilage architecture intact. Cartilage strength and function depend on both the properties of the tissue and on their structural parameters. The main structural macromolecules are collagen and proteoglycans (aggrecan). During life, cartilage matrix turnover is mediated by a multitude of complex autocrine and paracrine anabolic and catabolic factors. These act on the chondrocytes and can lead to repair, remodeling or catabolic processes like those that occur in osteoarthritis. Osteoarthritis is characterized by degradation and loss of articular cartilage, subchondral bone remodeling, and, at the clinical stage of the disease, inflammation of the synovial membrane. The alterations in osteoarthritic cartilage are numerous and involve morphologic and metabolic changes in chondrocytes, as well as biochemical and structural alterations in the extracellular matrix macromolecules.
引用
收藏
页码:351 / 384
页数:34
相关论文
共 203 条
[1]   STOP CODON IN THE PROCOLLAGEN-II GENE (COL2A1) IN A FAMILY WITH THE STICKLER SYNDROME (ARTHROOPHTHALMOPATHY) [J].
AHMAD, NN ;
ALAKOKKO, L ;
KNOWLTON, RG ;
JIMENEZ, SA ;
WEAVER, EJ ;
MAGUIRE, JI ;
TASMAN, W ;
PROCKOP, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (15) :6624-6627
[2]   Gene expression in chondrocytes assessed with use of microarrays [J].
Aigner, T ;
Zien, A ;
Hanisch, D ;
Zimmer, R .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2003, 85A :117-123
[3]   Genetic risk factors for lumbar disc disease [J].
Ala-Kokko, L .
ANNALS OF MEDICINE, 2002, 34 (01) :42-47
[4]   Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia [J].
Arikawa-Hirasawa, E ;
Le, AH ;
Nishino, I ;
Nonaka, I ;
Ho, NC ;
Francomano, CA ;
Govindraj, P ;
Hassell, JR ;
Devaney, JM ;
Spranger, J ;
Stevenson, RE ;
Iannaccone, S ;
Dalakas, MC ;
Yamada, Y .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (05) :1368-1375
[5]   Perlecan is essential for cartilage and cephalic development [J].
Arikawa-Hirasawa, E ;
Watanabe, H ;
Takami, H ;
Hassell, JR ;
Yamada, Y .
NATURE GENETICS, 1999, 23 (03) :354-358
[6]   Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene [J].
Arikawa-Hirasawa, E ;
Wilcox, WR ;
Le, AH ;
Silverman, N ;
Govindraj, P ;
Hassell, JR ;
Yamada, Y .
NATURE GENETICS, 2001, 27 (04) :431-434
[7]   Evaluation of thermoreversible polymers containing fibroblast growth factor 9 (FGF-9) for chondrocyte culture [J].
Au, A ;
Polotsky, A ;
Krzyminski, K ;
Gutowska, A ;
Hungerford, DS ;
Frondoza, CG .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2004, 69A (02) :367-372
[8]   Interleukin-1 in combination with oncostatin M up-regulates multiple genes in chondrocytes - Implications for cartilage destruction and repair [J].
Barksby, HE ;
Hui, W ;
Wappler, I ;
Peters, HH ;
Milner, JM ;
Richards, CD ;
Cawston, TE ;
Rowan, AD .
ARTHRITIS AND RHEUMATISM, 2006, 54 (02) :540-550
[9]   Genetic aspects of osteoarthritis [J].
Bateman, JF .
SEMINARS IN ARTHRITIS AND RHEUMATISM, 2005, 34 (06) :15-18
[10]   The molecular genetics of inherited cartilage disease [J].
Bateman, JF .
OSTEOARTHRITIS AND CARTILAGE, 2001, 9 :S141-S149