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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.
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页码:967 / 976
页数:10
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