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Experimental & Molecular Medicine ; : 424-431, 2012.
Artigo em Inglês | WPRIM | ID: wpr-119839

RESUMO

White fat cells secrete adipokines that induce inflammation and obesity has been reported to be characterized by high serum levels of inflammatory cytokines such as IL-6 and TNF-alpha. Rheumatoid arthritis (RA) is a prototype of inflammatory arthritis, but the relationship between RA and obesity is controversial. We made an obese inflammatory arthritis model: obese collagen-induced arthritis (CIA). C57BL/6 mice were fed a 60-kcal high fat diet (HFD) from the age of 4 weeks and they were immunized twice with type II collagen (CII). After immunization, the obese CIA mice showed higher arthritis index scores and histology scores and a more increased incidence of developing arthritis than did the lean CIA mice. After treatment with CII, mixed lymphocyte reaction also showed CII-specific response more intensely in the obese CIA mice than lean CIA. The anti-CII IgG and anti-CII IgG2a levels in the sera of the obese CIA mice were higher than those of the lean CIA mice. The number of Th17 cells was higher and the IL-17 mRNA expression of the splenocytes in the obese CIA mice was higher than that of the lean CIA mice. Obese CIA mice also showed high IL-17 expression on synovium in immunohistochemistry. Although obesity may not play a pathogenic role in initiating arthritis, it could play an important role in amplifying the inflammation of arthritis through the Th1/Th17 response. The obese CIA murine model will be an important tool when we investigate the effect of several therapeutic target molecules to treat RA.


Assuntos
Animais , Humanos , Camundongos , Adipocinas/imunologia , Artrite Experimental/genética , Diferenciação Celular/genética , Colágeno Tipo II/administração & dosagem , Modelos Animais de Doenças , Expressão Gênica , Inflamação/induzido quimicamente , Interleucina-17/metabolismo , Interleucina-6/sangue , Articulações/imunologia , Camundongos Endogâmicos C57BL , Obesidade/genética , Células Th17/imunologia , Fator de Necrose Tumoral alfa/sangue
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