The receptor S1P1 overrides regulatory T cell-mediated immune suppression through Akt-mTOR

被引:288
作者
Liu, Guangwei [1 ]
Burns, Samir [1 ]
Huang, Gonghua [1 ]
Boyd, Kelli [2 ]
Proia, Richard L. [3 ]
Flavell, Richard A. [4 ,5 ]
Chi, Hongbo [1 ,5 ]
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Anim Resources Ctr, Memphis, TN 38105 USA
[3] NIDDKD, Genet Dev & Dis Branch, NIH, Bethesda, MD 20892 USA
[4] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06510 USA
[5] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06510 USA
关键词
SPHINGOSINE 1-PHOSPHATE RECEPTOR; TOLL-LIKE; LYMPHOCYTE EGRESS; FOXP3; EXPRESSION; SPHINGOSINE-1-PHOSPHATE; FTY720; TRAFFICKING; REVERSAL; SURVIVAL; ANTIGEN;
D O I
10.1038/ni.1743
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells (T-reg cells) are critically involved in maintaining immunological tolerance, but this potent suppression must be 'quenched' to allow the generation of adaptive immune responses. Here we report that sphingosine 1-phosphate (S1P) receptor type 1 (S1P(1)) delivers an intrinsic negative signal to restrain the thymic generation, peripheral maintenance and suppressive activity of T-reg cells. Combining loss-and gain-of-function genetic approaches, we found that S1P1 blocked the differentiation of thymic T-reg precursors and function of mature T-reg cells and affected T-reg cell-mediated immune tolerance. S1P1 induced selective activation of the Akt-mTOR kinase pathway to impede the development and function of T-reg cells. Dynamic regulation of S1P1 contributed to lymphocyte priming and immune homeostasis. Thus, by antagonizing T-reg cell-mediated immune suppression, the lipid-activated S1P(1)-Akt-mTOR pathway orchestrates adaptive immune responses.
引用
收藏
页码:769 / U132
页数:11
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