Toll-like receptor-4 mediates lipopolysaccharide-induced signal transduction

被引:1607
作者
Chow, JC
Young, DW
Golenbock, DT
Christ, WJ
Gusovsky, F
机构
[1] Eisai Res Inst, Div Inflammatory Dis, Andover, MA 01810 USA
[2] Eisai Res Inst, Div Synthet Chem, Andover, MA 01810 USA
[3] Boston Univ, Boston Med Ctr, Sch Med, Maxwell Finland Lab Infect Dis, Boston, MA 02118 USA
关键词
D O I
10.1074/jbc.274.16.10689
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
TLR4 is a member of the recently identified Toll-like receptor family of proteins and has been putatively identified as Lps, the gene necessary for potent responses to lipopolysaccharide in mammals. In order to determine whether TLR4 is involved in lipopolysaccharide-induced activation of the nuclear factor-kappa B (NF-kappa B) pathway, HEK 293 cells were transiently transfected with human TLR4 cDNA and an NF-kappa B-dependent luciferase reporter plasmid followed by stimulation with lipopolysaccharide/CD14 complexes. The results demonstrate that lipopolysaccharide stimulates NF-kappa B-mediated gene expression in cells transfected with the TLR4 gene in a dose- and time-dependent fashion. Furthermore, E5531, a lipopolysaccharide antagonist, blocked TLR4-mediated transgene activation in a dose-dependent manner (IC50 similar to 30 nM). These data demonstrate that TLR4 is involved in lipopolysaccharide signaling and serves as a cell-surface co-receptor for CD14, leading to lipopolysaccharide-mediated NF-kappa B activation and subsequent cellular events.
引用
收藏
页码:10689 / 10692
页数:4
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