E-73, an acetoxyl analogue of cycloheximide, blocks the tumor necrosis factor-induced NF-κB signaling pathway

被引:25
作者
Sugimoto, H
Kataoka, T
Igarashi, M
Hamada, M
Takeuchi, T
Nagai, K
机构
[1] Tokyo Inst Technol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[2] Inst Microbial Chem, Shinagawa Ku, Tokyo 1410021, Japan
关键词
cycloheximide; E-73; ICAM-1; I kappa B; NF-kappa B; TNF;
D O I
10.1006/bbrc.2000.3680
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proinflammatory cytokines such as tumor necrosis factor (TNF) and interleukin (IL)-1 activate the NF-kappaB signaling pathway which induces the expression of a variety of genes such as the encoding intercellular adhesion molecule (ICAM)-1, We have found that E-73, an acetoxyl analogue of cycloheximide, specifically blocks TNF-induced ICAM-1 expression even at concentrations unable to affect protein synthesis. By contrast, cycloheximide inhibited both TNF- and IL-1-induced ICAM-1 expression primarily due to the blockage of protein synthesis. The nuclear translocation of NF-kappaB as well as the I kappaB degradation induced by TNF, but not by IL-1, was significantly prevented by E-73, These observations suggest that E-73 blocks the TNF-induced NF-kappaB signaling pathway upstream of I kappaB degradation. (C) 2000 Academic Press.
引用
收藏
页码:330 / 333
页数:4
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