Artemisolide is a typical inhibitor of IκB kinase β targeting cysteine-179 residue and down-regulates NF-κB-dependent TNF-α expression in LPS-activated macrophages

被引:24
|
作者
Kim, Byung Hak
Lee, Jun-Young
Seo, Jee Hee
Lee, Hwa Young
Ryu, Shi Yong
Ahn, Byung Woo
Lee, Chong-Kii
Hwang, Bang Yeon
Han, Sang-Bae
Kim, Youngsoo [1 ]
机构
[1] Chungbuk Natl Univ, Coll Pharm, Cheongju 361763, South Korea
[2] Korea Res Inst Chem Technol, Taejon 305600, South Korea
[3] Chungbuk Natl Univ, Coll Vet Med, Cheongju 361763, South Korea
关键词
artemisolide; IKK beta activity; NF-kappa B activation; TNF-alpha; expression; LPS-activated inacropliages;
D O I
10.1016/j.bbrc.2007.07.069
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
Nuclear factor (NF)-kappa B regulates a central common signaling for immunity and cell survival. Artemisolide (ATM) was previously isolated as a NIF-kappa B inhibitor from a plant of Artemisia asiatica. However, molecular basis of ATM on NF-kappa B activation remains to be defined. Here, we demonstrate that ATM is a typical inhibitor of I kappa B kinase beta(IKK beta), resulting in inhibition of lipopolysaccharide (LPS)-induced NF-kappa B activation in RAW 264.7 macrophages. ATM inhibited the kinase activity of highly purified IKK beta and also LPS-induced IKK activity in the cells. Moreover, the effect of ATM on IKK beta activity was completely abolished by substitution of Cys-179 residue of IKK beta to Ala residue, indicating direct targeting site of ATM. ATM could inhibit I kappa B alpha. phosphorylation in LPS-activated RAW 264.7 cells and subsequently prevent NF-kappa B activation. Further, we demonstrate that ATM clown-regulates NF-kappa B-dependent TNF-alpha expression. Taken together, this study provides a pharmacological potential of ATM in NF-kappa B-dependent inflammatory disorders. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:593 / 598
页数:6
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