Glycyrrhizin and isoliquiritigenin suppress the LPS sensor Toll-like receptor 4/MD-2 complex signaling in a different manner

被引:94
作者
Honda, Hiroe [1 ,2 ,3 ]
Nagai, Yoshinori [1 ]
Matsunaga, Takayuki [3 ]
Saitoh, Shin-ichiro [4 ]
Akashi-Takamura, Sachiko [4 ]
Hayashi, Hiroaki [5 ]
Fujii, Isao [5 ]
Miyake, Kensuke [4 ]
Muraguchi, Atsushi [2 ]
Takatsu, Kiyoshi [1 ,3 ]
机构
[1] Toyama Univ, Grad Sch Med & Pharmaceut Sci Res, Dept Immunobiol & Pharmacol Genet, Toyama 9300194, Japan
[2] Toyama Univ, Grad Sch Med & Pharmaceut Sci Res, Dept Immunol, Toyama 9300194, Japan
[3] Toyama Prefectural Inst Pharmaceut Res, Toyama, Japan
[4] Univ Tokyo, Inst Med Sci, Dept Microbiol & Immunol, Div Infect Genet, Tokyo, Japan
[5] Iwate Med Univ, Sch Pharm, Dept Nat Prod Chem, Morioka, Iwate, Japan
基金
日本学术振兴会;
关键词
innate immunity; Glycyrrhiza uralensis; NF-kappa B; MAPK; IL-6; MOUSE PERITONEAL-MACROPHAGES; MEN-DONG-TANG; NF-KAPPA-B; SCAVENGER RECEPTOR; INFLAMMATORY RESPONSES; ANTITUSSIVE PRINCIPLES; MAIN COMPONENT; PANAX-GINSENG; CUTTING EDGE; LIPOPOLYSACCHARIDE;
D O I
10.1189/jlb.0112038
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent evidences suggest that the extracts of plant products are able to modulate innate immune responses. A saponin GL and a chalcone ILG are representative components of Glycyrrhiza uralensis, which attenuate inflammatory responses mediated by TLRs. Here, we show that GL and ILG suppress different steps of the LPS sensor TLR4/MD-2 complex signaling at the receptor level. Extract of G. uralensis suppressed IL-6 and TNF-alpha production induced by lipid A moiety of LPS in RAW264.7 cells. Among various G. uralensis-related components of saponins and flavanones/chalcones, GL and ILG could suppress IL-6 production induced by lipid A in dose-dependent manners in RAW264.7 cells. Furthermore, elevation of plasma TNF-alpha in LPS-injected mice was attenuated by passive administration of GL or ILG. GL and ILG inhibited lipid A-induced NF-kappa B activation in Ba/F3 cells expressing TLR4/MD-2 and CD14 and BMMs. These components also inhibited activation of MAPKs, including JNK, p38, and ERK in BMMs. In addition, GL and ILG inhibited NF-kappa B activation and IL-6 production induced by paclitaxel, a nonbacterial TLR4 ligand. Interestingly, GL attenuated the formation of the LPS-TLR4/MD-2 complexes, resulting in inhibition of homodimerization of TLR4. Although ILG did not affect LPS binding to TLR4/MD-2, it could inhibit LPS-induced TLR4 homodimerization. These results imply that GL and ILG modulate the TLR4/MD-2 complex at the receptor level, leading to suppress LPS-induced activation of signaling cascades and cytokine production, but their effects are exerted at different steps of TLR4/MD-2 signaling. J. Leukoc. Biol. 91: 967-976; 2012.
引用
收藏
页码:967 / 976
页数:10
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