Dioscorin isolated from Dioscorea alata activates TLR4-signaling pathways and induces cytokine expression in macrophages

被引:60
作者
Fu, SL
Hsu, YH
Lee, PY
Hou, WC
Hung, LC
Lin, CH
Chen, CM
Huang, YJ
机构
[1] Natl Yang Ming Univ, Inst Tradit Med, Taipei 11221, Taiwan
[2] Bur Food & Drug Analysis, Dept Hlth, Taipei 11221, Taiwan
[3] Taipei Med Univ, Grad Inst Pharmacognosy Sci, Taipei 11221, Taiwan
[4] Natl Yang Ming Univ, Dept Life Sci, Taipei 11221, Taiwan
关键词
dioscorin; Dioscorea alata; TLR4; NF-kappa B; MAPK; cytokine;
D O I
10.1016/j.bbrc.2005.11.005
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
The Toll-like receptor 4 (TLR4)-signaling pathway is crucial for activating both innate and adaptive immunity. TLR4 is a promising molecular target for immune-modulating drugs, and TLR4 agonists are of therapeutic potential for treating immune diseases and cancers. Several medicinal herb-derived components have recently been reported to act via TLR4-dependant pathway, suggesting that medicinal plant are potential resources for identifying TLR4 activators. We have applied a screening procedure to systematically identify herbal constituents that active TLR4. To exclude possible LPS contamination in these plant-derived components, a LPS inhibitor, polymyxin B, was added during screening. One of the plant components we identified from the screening was dioscorin, the glycoprotein isolated from Dioscorea alata. It induced TLR4-downstream cytokine expression in bone marrow cells isolated from TRL4-functional C3H/HeN mice but not from TLR4-defective C3H/HeJ mice. Dioscorin also stimulated multiple signaling molecules (NF-kappa B, ERK, JNK, and p38) and induced the expression of cytokines (TNF-alpha, IL-1 beta, and IL-6) in murine RAW 264.7 macrophages. Furthermore, the ERK, p38, JNK, and NF-kappa B-mediated pathways are all involved in dioscorin-mediated TNF-alpha production. In summary, our results demonstrate that dioscorin is a novel TRL4 activator and induces macrophage activation via typical TLR4-signaling pathways. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:137 / 144
页数:8
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