The Role of Inflammatory and Anti-Inflammatory Cytokines in the Pathogenesis of Osteoarthritis

被引:1560
作者
Wojdasiewicz, Piotr [1 ]
Poniatowski, Lukasz A. [1 ]
Szukiewicz, Dariusz [1 ]
机构
[1] Med Univ Warsaw, Fac Med 2, Dept Gen & Expt Pathol, PL-02106 Warsaw, Poland
关键词
TUMOR-NECROSIS-FACTOR; NF-KAPPA-B; HUMAN ARTICULAR CHONDROCYTES; GROWTH-FACTOR-BETA; NITRIC-OXIDE PRODUCTION; INSTABILITY-INDUCED OSTEOARTHRITIS; INTERLEUKIN-1 RECEPTOR ANTAGONIST; POTENTIAL THERAPEUTIC TARGET; ACTIVATED PROTEIN-KINASE; INFRAPATELLAR FAT PAD;
D O I
10.1155/2014/561459
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Osteoarthritis (OA) is the most common chronic disease of human joints. The basis of pathologic changes involves all the tissues forming the joint; already, at an early stage, it has the nature of inflammation with varying degrees of severity. An analysis of the complex relationships indicates that the processes taking place inside the joint are not merely a set that ( seemingly) only includes catabolic effects. Apart from them, anti-inflammatory anabolic processes also occur continually. These phenomena are driven by various mediators, of which the key role is attributed to the interactions within the cytokine network. The most important group controlling the disease seems to be inflammatory cytokines, including IL-1 beta, TNF alpha, IL-6, IL-15, IL-17, and IL-18. The second group with antagonistic effect is formed by cytokines known as anti-inflammatory cytokines such as IL-4, IL-10, and IL-13. The role of inflammatory and anti-inflammatory cytokines in the pathogenesis of OA with respect to inter-and intracellular signaling pathways is still under investigation. This paper summarizes the current state of knowledge. The cytokine network in OA is put in the context of cells involved in this degenerative joint disease. The possibilities for further implementation of new therapeutic strategies in OA are also pointed.
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页数:19
相关论文
共 251 条
[1]
Inflammation in osteoarthritis [J].
Goldring, Mary B. ;
Otero, Miguel .
CURRENT OPINION IN RHEUMATOLOGY, 2011, 23 (05) :471-478
[2]
Reactive oxygen species and superoxide dismutases: Role in joint diseases [J].
Afonso, Valery ;
Champy, Rornuald ;
Mitrovic, Dragoslav ;
Collin, Pascal ;
Lomri, Abderrahim .
JOINT BONE SPINE, 2007, 74 (04) :324-329
[3]
Gene expression profiling of serum- and interleukin-1β-stimulated primary human adult articular chondrocytes -: A molecular analysis based on chondrocytes isolated from one donor [J].
Aigner, T ;
McKenna, L ;
Zien, A ;
Fan, ZY ;
Gebhard, PM ;
Zimmer, R .
CYTOKINE, 2005, 31 (03) :227-240
[4]
Alaaeddine N, 1997, J RHEUMATOL, V24, P1985
[5]
Alaaeddine N, 1999, ARTHRITIS RHEUM-US, V42, P710, DOI 10.1002/1529-0131(199904)42:4<710::AID-ANR14>3.0.CO
[6]
2-4
[7]
Alaaeddine N, 2001, ARTHRITIS RHEUM-US, V44, P1633, DOI 10.1002/1529-0131(200107)44:7<1633::AID-ART286>3.0.CO
[8]
2-Z
[9]
CELLULAR IMMUNE-RESPONSE TOWARD HUMAN ARTICULAR CHONDROCYTES - T-CELL REACTIVITIES AGAINST CHONDROCYTE AND FIBROBLAST MEMBRANES IN DESTRUCTIVE JOINT DISEASES [J].
ALSALAMEH, S ;
MOLLENHAUER, J ;
HAIN, N ;
STOCK, KP ;
KALDEN, JR ;
BURMESTER, GR .
ARTHRITIS AND RHEUMATISM, 1990, 33 (10) :1477-1486
[10]
DEVELOPMENT OF CRITERIA FOR THE CLASSIFICATION AND REPORTING OF OSTEOARTHRITIS - CLASSIFICATION OF OSTEOARTHRITIS OF THE KNEE [J].
ALTMAN, R ;
ASCH, E ;
BLOCH, D ;
BOLE, G ;
BORENSTEIN, D ;
BRANDT, K ;
CHRISTY, W ;
COOKE, TD ;
GREENWALD, R ;
HOCHBERG, M ;
HOWELL, D ;
KAPLAN, D ;
KOOPMAN, W ;
LONGLEY, S ;
MANKIN, H ;
MCSHANE, DJ ;
MEDSGER, T ;
MEENAN, R ;
MIKKELSEN, W ;
MOSKOWITZ, R ;
MURPHY, W ;
ROTHSCHILD, B ;
SEGAL, M ;
SOKOLOFF, L ;
WOLFE, F .
ARTHRITIS AND RHEUMATISM, 1986, 29 (08) :1039-1049