RANKL synthesized by articular chondrocytes contributes to juxta-articular bone loss in chronic arthritis

被引:47
|
作者
Martinez-Calatrava, Maria J. [1 ]
Prieto-Potin, Ivan [1 ]
Roman-Blas, Jorge A. [1 ]
Tardio, Lidia [1 ]
Largo, Raquel [1 ]
Herrero-Beaumont, Gabriel [1 ]
机构
[1] Univ Autonoma Madrid, IIS Fdn Jimenez Az D237, Bone & Joint Res Unit, Serv Rheumatol, Madrid 28040, Spain
关键词
KAPPA-B LIGAND; OSTEOCLAST DIFFERENTIATION FACTOR; COLLAGEN-INDUCED ARTHRITIS; RHEUMATOID-ARTHRITIS; RECEPTOR ACTIVATOR; SYNOVIAL TISSUE; OSTEOPROTEGERIN LIGAND; INFLAMMATORY ARTHRITIS; IN-VITRO; T-CELLS;
D O I
10.1186/ar3884
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The receptor activator nuclear factor-kappaB ligand (RANKL) diffuses from articular cartilage to subchondral bone. However, the role of chondrocyte-synthesized RANKL in rheumatoid arthritis-associated juxta-articular bone loss has not yet been explored. This study aimed to determine whether RANKL produced by chondrocytes induces osteoclastogenesis and juxta-articular bone loss associated with chronic arthritis. Methods: Chronic antigen-induced arthritis (AIA) was induced in New Zealand (NZ) rabbits. Osteoarthritis (OA) and control groups were simultaneously studied. Dual X-ray absorptiometry of subchondral knee bone was performed before sacrifice. Histological analysis and protein expression of RANKL and osteoprotegerin (OPG) were evaluated in joint tissues. Co-cultures of human OA articular chondrocytes with peripheral blood mononuclear cells (PBMCs) from healthy donors were stimulated with macrophage-colony stimulating factor (M-CSF) and prostaglandin E-2 (PGE(2)), then further stained with tartrate-resistant acid phosphatase. Results: Subchondral bone loss was confirmed in AIA rabbits when compared with controls. The expression of RANKL, OPG and RANKL/OPG ratio in cartilage were increased in AIA compared to control animals, although this pattern was not seen in synovium. Furthermore, RANKL expression and RANKL/OPG ratio were inversely related to subchondral bone mineral density. RANKL expression was observed throughout all cartilage zones of rabbits and was specially increased in the calcified cartilage of AIA animals. Co-cultures demonstrated that PGE(2)-stimulated human chondrocytes, which produce RANKL, also induce osteoclasts differentiation from PBMCs. Conclusions: Chondrocyte-synthesized RANKL may contribute to the development of juxta-articular osteoporosis associated with chronic arthritis, by enhancing osteoclastogenesis. These results point out a new mechanism of bone loss in patients with rheumatoid arthritis.
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页数:13
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