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Evaluation of cartilage and bone degradation in a murine collagen antibody-induced arthritis model
被引:21
|作者:
Oestergaard, S.
[1
]
Rasmussen, K. E.
[1
]
Doyle, N.
[2
]
Varela, A.
[2
]
Chouinard, L.
[2
]
Smith, S. Y.
Qvist, P.
[1
]
Karsdal, M. A.
[1
]
机构:
[1] Nordic Biosci AS, DK-2730 Herlev, Denmark
[2] Transcanadienne, Preclin Serv Montreal, Charles River Lab, Senneville, PQ, Canada
关键词:
D O I:
10.1111/j.1365-3083.2007.02060.x
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
The purpose of this work was to validate collagen antibody-induced arthritis (CAIA) model in two mice strains (Balb/c and CD-1) using clinical, biochemical, microstructural and histological techniques. We induced arthritis in mice using a cocktail of collagen type II (CII) antibodies followed by an injection with lipopolysaccharide (LPS) in different doses in Balb/c and CD-1 mice strains. Serum CTX-II levels were measured at study termination and correlated with microscopic severity of joint lesions as determined by a validated scoring systems. Bone involvement was assessed by microcomputer tomography (micro-CT). Balb/c mice developed rapid (day 6) and robust (100%) arthritis, whereas CD-1 mice showed only temporary macroscopic signs of disease. Serum CTX-II levels in Balb/c mice showed a significant increase in cartilage degradation in diseased animals (43-64% compared with non-diseased mice) and was decreased in animals receiving dexamethasone. Correlation of serum CTX-II with the microscopic score was statistically significant (P < 0.01). Micro-CT analysis demonstrated structural damage in bone in the CAIA Balb/c mice, which was prevented by dexamethasone. The CAIA-LPS model provides a useful supplement to currently available animal models of arthritis. This is a rapid onset and robust model; however, the choice of mouse strain should be evaluated carefully.
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页码:304 / 312
页数:9
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