Galectin-9 promotes TGF-β1-dependent induction of regulatory T cells via the TGF-β/Smad signaling pathway

被引:38
作者
Lv, Kun [1 ]
Zhang, Yingying
Zhang, Mengying [1 ]
Zhong, Min [1 ]
Suo, Qifeng [1 ]
机构
[1] Wannan Med Coll, Yijishan Hosp, Cent Lab, Wuhu 241001, Peoples R China
关键词
galectin-9; regulatory T cells; conversion; phosphorylation; CUTTING EDGE; BETA; CONVERSION; EXPANSION; MICE; PROLIFERATION; HOMEOSTASIS; DISRUPTION; EXPRESSION; TOLERANCE;
D O I
10.3892/mmr.2012.1125
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
TGF-beta 1 induces the conversion of CD4(+)CD25(-) T cells into CD4(+)CD25(+)Foxp3(+) regulatory T cells (Tregs). Galectin-9, one of the beta-galactoside-binding animal lectins belonging to the galectin family, induces apoptosis of eosinophils, cancer cells and T cells. In this study, we report the effects of galectin-9 on the conversion of CD4(+)CD25(-) T cells into Foxp3-expressing induced Tregs (iTregs). Galectin-9 together with TGF-beta 1 had synergistic effects on the rate of conversion to iTregs in vitro. TGF-beta 1 signaling appears to be essential for the effects of galectin-9 on the generation of iTregs, as galectin-9 promotes TGF-beta 1-induced phosphorylation of Smad2/3, ERK1/2 and formation of the Smad2/3-Smad4 complex. These data suggest a role for galectin-9 as a promoter of the TGF-beta 1-dependent conversion of CD4(+)CD25(-) T cells into iTregs in vitro. Therefore, in addition to inducing apoptosis, galectin-9 may contribute to the regulation of inflammation via the expansion of peripheral Tregs.
引用
收藏
页码:205 / 210
页数:6
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