Icariin and its derivative, ICT, exert anti-inflammatory, anti-tumor effects, and modulate myeloid derived suppressive cells (MDSCs) functions

被引:131
|
作者
Zhou, Junmin [1 ]
Wu, Jinfeng [2 ]
Chen, Xianghong [1 ]
Fortenbery, Nicole [1 ]
Eksioglu, Erika [1 ]
Kodumudi, Krithika N. [1 ]
Pk, Epling-Bumette [1 ]
Dong, Jingcheng [2 ]
Djeu, Julie Y. [1 ]
Wei, Sheng [1 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Dept Immunol, Tampa, FL 33612 USA
[2] Fudan Univ, Dept Integrat Med, Huashan Hosp, Shanghai 200040, Peoples R China
基金
美国国家卫生研究院;
关键词
MDSC; ICA; ICT; Inflammation; TLR4; MRP8/14; TOLL-LIKE RECEPTOR; CANCER; INFLAMMATION; TLR4; MICE; DIFFERENTIATION; RESPONSES; S100A9; ACCUMULATION; INHIBITION;
D O I
10.1016/j.intimp.2011.01.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
3, 5, 7-Trihydroxy-4'-methoxy-8-(3-hydroxy-3-methylbutyl)-flavone (ICT) is a novel derivative of Icariin (ICA), the major active ingredient of Herba Epimedii, a herb used in traditional Chinese and alternative medicine. We previously demonstrated its anti-inflammatory effect in murine innate immune cells and activated human PBMCs. We report herein that ICA or ICT treatment reduces the expression of MRP8/MRP14 and toll-like receptor 4 (TLR4) on human PBMCs. Administration of ICA or ICT inhibited tumor growth in 4T1-Neu tumor-bearing mice and considerably decreased MDSC numbers in the spleen of these mice. Further, we saw a restoration of IFN-gamma production by CD8(+) T cells in tumor bearing mice when treated with ICA or ICT. ICA and ICT significantly decreased the amounts of nitric oxide and reactive oxygen species in MDSC in vivo. When MDSC were treated in vitro with ICT, we saw a significant reduction in the percent of these cells with concomitant differentiation into dendritic cells and macrophages. Concomitant with this cell type conversion was a down-regulation of IL-10, IL-6 and TNF-alpha production. Decreased expression of S100A8/9 and inhibition of activation of STAT3 and AKT may in part be responsible for the observed results. In conclusion, our results showed that ICA, and more robustly, ICT, directly modulate MDSC signaling and therefore altered the phenotype and function of these cells, in vitro and in vivo. (c) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:890 / 898
页数:9
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