Santonin-related compound 2 inhibits the expression of ICAM-1 in response to IL-1 stimulation by blocking the signaling pathway upstream of IκB degradation

被引:29
作者
Kawai, S
Kataoka, T
Sugimoto, H
Nakamura, A
Kobayashi, T
Arao, K
Higuchi, Y
Ando, M
Nagai, K
机构
[1] Tokyo Inst Technol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[2] Niigata Univ, Fac Engn, Dept Appl Chem, Niigata 9502181, Japan
来源
IMMUNOPHARMACOLOGY | 2000年 / 48卷 / 02期
关键词
ICAM-1; IL-1; inflammation; NF-kappa B; L-alpha-santonin;
D O I
10.1016/S0162-3109(00)00196-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
Santonin-related compounds (SRCs) were synthesized from the starting material L-alpha-santonin and tested for the biological activity on the expression of intercellular adhesion molecule-1 (ICAM-1) in response to IL-1 stimulation on human adenocarcinoma cells, One of the bromoketone derivatives termed SRC2 [(11S)-2 alpha-bromo-3-oxoeudesmanno-13,6 alpha-lactone] strongly inhibited the ICAM-1 expression at an IC50 value of 5.9 mu M, whereas L-alpha-santonin itself was totally inactive up to 100 mu M The blockage of ICAM-1 expression by SRC2 was not due to the direct inhibition of de novo RNA and protein synthesis, The nuclear translocation of NF-kappa B subunit p65 was markedly prevented by SRC2, Moreover, I kappa B alpha degradation upon IL-1 stimulation was strongly inhibited by SRC2. These observations suggest that SRC2 blocks the IL-1 signaling pathway upstream of I kappa B degradation. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:129 / 135
页数:7
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