Membrane-bound Dickkopf-1 in Foxp3+ regulatory T cells suppresses T-cell-mediated autoimmune colitis

被引:18
作者
Chae, Wook-Jin [1 ]
Park, Jong-Hyun [2 ]
Henegariu, Octavian [3 ]
Yilmaz, Saliha [3 ]
Hao, Liming [4 ]
Bothwell, Alfred L. M. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[2] KIST, Treatment & Care Syst Dementia, Convergence Res Ctr Diag, Seoul, South Korea
[3] Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT USA
[4] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06510 USA
关键词
autoimmune colitis; Dickkopf-1; regulatory T cells; WNT ANTAGONIST DICKKOPF-1; MASTER REGULATOR; EXPRESSION; RECEPTOR; THERAPY; DKK1;
D O I
10.1111/imm.12766
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Induction of tolerance is a key mechanism to maintain or to restore immunological homeostasis. Here we show that Foxp3(+) regulatory T (Treg) cells use Dickkopf-1 (DKK-1) to regulate T-cell-mediated tolerance in the T-cell-mediated autoimmune colitis model. Treg cells from DKK-1 hypomorphic doubleridge mice failed to control CD4(+) T-cell proliferation, resulting in CD4 T-cell-mediated autoimmune colitis. Thymus-derived Treg cells showed a robust expression of DKK-1 but not in naive or effector CD4 T cells. DKK-1 expression in Foxp3(+) Treg cells was further increased upon T-cell receptor stimulation in vitro and in vivo. Interestingly, Foxp3(+) Treg cells expressed DKK-1 in the cell membrane and the functional inhibition of DKK-1 using DKK-1 monoclonal antibody abrogated the suppressor function of Foxp3(+) Treg cells. DKK-1 expression was dependent on de novo protein synthesis and regulated by the mitogen-activated protein kinase pathway but not by the canonical Wnt pathway. Taken together, our results highlight membrane-bound DKK-1 as a novel Treg-derived mediator to maintain immunological tolerance in T-cell-mediated autoimmune colitis.
引用
收藏
页码:265 / 275
页数:11
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