Periarticular Bone Loss in Antigen-Induced Arthritis

被引:24
作者
Engdahl, Cecilia [1 ]
Lindholm, Catharina [1 ]
Stubelius, Alexandra [1 ]
Ohlsson, Claes [1 ]
Carlsten, Hans [1 ]
Lagerquist, Marie K. [1 ]
机构
[1] Univ Gothenburg, S-40530 Gothenburg, Sweden
来源
ARTHRITIS AND RHEUMATISM | 2013年 / 65卷 / 11期
基金
瑞典研究理事会;
关键词
COLONY-STIMULATING FACTOR; TUMOR-NECROSIS-FACTOR; RHEUMATOID-ARTHRITIS; T-CELLS; INFLAMMATORY ARTHRITIS; GENE-EXPRESSION; SYNOVIAL-FLUID; NUCLEAR-FACTOR; FREE-RADICALS; TNF-ALPHA;
D O I
10.1002/art.38114
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveBone loss in arthritis is a complex process characterized by bone erosions and periarticular and generalized bone loss. The antigen-induced arthritis (AIA) model is mainly used to study synovitis and joint destruction, including bone erosions; however, periarticular bone loss has been less extensively investigated. The objectives of this study were to characterize and establish AIA as a model for periarticular bone loss, and to determine the importance of NADPH oxidase 2 (NOX-2)-derived reactive oxygen species (ROS) in periarticular bone loss. MethodsArthritis was induced in mice by local injection of antigen in one knee; the other knee was used as a nonarthritis control. At study termination, the knees were collected for histologic assessment. Periarticular bone mineral density (BMD) was investigated by peripheral quantitative computed tomography. Flow cytometric analyses were performed using synovial and bone marrow cells. ResultsAIA resulted in decreased periarticular trabecular BMD and increased frequencies of preosteoclasts, neutrophils, and monocytes in the arthritic synovial tissue. Arthritis induction resulted in an increased capability to produce ROS. However, induction of arthritis in Ncf1*(/)* mice, which lack NOX-2-derived ROS, and control mice resulted in similar reductions in periarticular trabecular BMD. ConclusionThe initiation of AIA resulted in periarticular bone loss associated with local effects on inflammatory cells and osteoclasts. Furthermore, based on our observations using this model, we conclude that NOX-2-derived ROS production is not essential for inflammation-mediated periarticular bone loss. Thus, AIA can be used as a model to investigate the pathogenesis of local inflammation-mediated bone loss.
引用
收藏
页码:2857 / 2865
页数:9
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