Differential anti-inflammatory pathway by xanthohumol in IFN-γ and LPS-activated macrophages

被引:107
作者
Cho, Young-Chang [1 ,2 ]
Kim, Hyun Jung [1 ,2 ]
Kim, Young-Jun [1 ,2 ]
Lee, Kwang Youl [1 ,2 ]
Choi, Hyun Jin [1 ,2 ]
Lee, Ik-Soo [1 ,2 ]
Kang, Bok Yun [1 ,2 ]
机构
[1] Chonnam Natl Univ, Coll Pharm, Kwangju 500757, South Korea
[2] Chonnam Natl Univ, Res Inst Drug Dev, Kwangju 500757, South Korea
关键词
xanthohumol; inflammation; interferon-gamma; lipopolysaccharide; RAW264.7;
D O I
10.1016/j.intimp.2007.12.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Macrophages are the main cells responsible for the innate immunity, and their activation by tipopolysaccharide (LPS) from Gram-negative bacteria or interferon (IFN)-gamma from host immune cells is important for controlling infections. However, the overwhelming activation of macrophages can cause a severe inflammatory state. This study investigated the inhibitory mechanism of xanthohumot (XN) against the inflammatory effectors (IL-1 beta, TNF-alpha, and iNOS) in activated RAW264.7 macrophages by using different stimuli such as LPS, IFN-gamma, or LPS plus IFN-gamma. XN is a major prenylated chalcone found in hops, which is used to add bitterness and flavor to beer. XN reduced the expression of the LPS receptor components such as TLR4 and MD2 resulting in the suppression of NF-kappa B activation in LPS-activated RAW264.7 cells. In the IFN-gamma stimulated RAW264.7 cells, the binding activity of STAT-1 alpha and IRF-1 was inhibited by XN. This suggests that differential signaling pathways are used by XN for the inhibition of excess inflammatory mediators depending on the stimuli in macrophages. (c)) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:567 / 573
页数:7
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