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International Immunology, Vol. 11, No. 2, 151-158, February 1999
© 1999 Japanese Society for Immunology

Inhibition of IL-6 and IL-8 induction from cultured rheumatoid synovial fibroblasts by treatment with aurothioglucose

Shin-ichi Yoshida1,2, Tetsuji Kato1,2, Shinsaku Sakurada1, Chieko Kurono3, Jian-Ping Yang1, Nobuo Matsui2, Tsuyoshi Soji3 and Takashi Okamoto1

1 Departments of Molecular Genetics,
2 Orthopedics and
3 Anatomy I,Nagoya City University Medical School, 1 Kawasumi, Mizuho-cho, Mizuho-ku,Nagoya 467-8601, Japan

Correspondence to: T. Okamoto

Gold compounds have long been used in the treatment of rheumatoid arthritis (RA). However, their actions in RA have not been clarified. In this study, we examined the effect of one of the monovalent gold compounds, aurothioglucose (AuTG), on the IL-1-induced production of IL-6, IL-8 and granulocyte macrophage colony stimulating factor (GM-CSF) from rheumatoid synovial fibroblasts (RSF) isolated from three RA patients. IL-6 and IL-8 induction but not GM-CSF induction was inhibited in most of the RSF after pretreatment with AuTG. Since gene expression of these cytokines is known to be under the control of a common transcription factor, NF-{kappa}B, the effect of AuTG on the cellular localization of NF-{kappa}B (p65 subunit) and on NF-{kappa}B–DNA binding was examined. Although AuTG treatment did not prevent NF-{kappa}B nuclear translocation, AuTG blocked the DNA-binding activity of NF-{kappa}B when examined in vitro. Morphologically, both metal-specific cell staining using p-dimethylaminobenzylidene rhodamine and transmission electron microscopic examinations demonstrated the accumulation of metal gold in the cytoplama and some organella (mitochondria and lysosomes) of the AuTG-treated RSF. These results indicate that one of the anti-rheumatic actions of AuTG might be through its inhibitory action on NF-{kappa}B.

Keywords: electron microscopy, NF-{kappa}B, redox regulation

Transmitting editor: K. Okumura


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