Green tea EGCG suppresses T cell proliferation through impairment of IL-2/IL-2 receptor signaling

被引:82
作者
Wu, Dayong [1 ]
Guo, Zhuyan [1 ]
Ren, Zhihong [1 ]
Guo, Weimin [2 ]
Meydani, Simin Nikbin [1 ]
机构
[1] Tufts Univ, Jean Mayer USDA Human Nutr Res Ctr, Nutr Immunol Lab, Boston, MA 02111 USA
[2] Tufts Univ, Jean Mayer USDA Human Nutr Res Ctr, Vasc Biol Lab, Boston, MA 02111 USA
关键词
Green tea; EGCG; Immune function; T cells; Interleukin-2; VITAMIN-E; GENE-EXPRESSION; IFN-GAMMA; IN-VITRO; INHIBITION; EPIGALLOCATECHIN-3-GALLATE; POLYPHENOLS; GALLATE; (-)-EPIGALLOCATECHIN-3-GALLATE; CATECHINS;
D O I
10.1016/j.freeradbiomed.2009.06.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Studies have suggested a benefit of consuming green tea in promoting general health and reducing the risk of certain diseases. However, little is known about the effect of green tea on immune function. In this study we determined the effect of epigallocatechin-3-gallate (EGCG), the major active component of tea, on proliferation of spleen cells isolated from C57BL mice. Results showed that T cell proliferation was inhibited by EGCG at physiologically relevant concentrations of 2.5 to 10 mu M EGCG at these concentrations did not induce cytotoxicity or apoptosis. Oxidative stress is not likely to be responsible for the EGCG-induced suppression of T cell proliferation because H2O2 generation was not significantly different between the cultures supplemented with 1 to 10 mu M EGCG and control and catalase did not prevent this EGCG-induced inhibition. Further mechanistic studies showed that EGCG dose dependently inhibited T cell division and cell cycle progression. EGCG supplementation resulted in lower IL-2 receptor expression and higher IL-2 accumulation, suggesting an impeded IL-2/IL-2 receptor signaling. These results indicate that EGCG supplementation may be beneficial to those with abnormally excessive T cell function such as autoimmune and inflammatory disorders, but caution should be taken when it is administered at high doses to those with compromised T cell function. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:636 / 643
页数:8
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