Foxo1 links homing and survival of naive T cells by regulating L-selectin, CCR7 and interleukin 7 receptor

被引:422
作者
Kerdiles, Yann M. [1 ,2 ]
Beisner, Daniel R. [1 ,2 ]
Tinoco, Roberto [1 ,2 ]
Dejean, Anne S. [1 ,2 ]
Castrillon, Diego H. [3 ,4 ,5 ]
DePinho, Ronald A. [3 ,4 ,5 ]
Hedrick, Stephen M. [1 ,2 ]
机构
[1] Univ Calif San Diego, Mol Biol Sect, Div Biol Sci, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[3] Harvard Univ, Sch Med, Dana Farber Canc Inst,Dept Adult Oncol, Ctr Appl Canc Sci,Belfer Inst Innovat Canc Sci, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Genet, Boston, MA 02115 USA
关键词
TRANSCRIPTION FACTORS; PHOSPHATIDYLINOSITOL; 3-KINASE; TRANSGENIC MICE; FAMILY-MEMBER; FORKHEAD; HOMEOSTASIS; EXPRESSION; IL-7; LYMPHOCYTE; ACTIVATION;
D O I
10.1038/ni.1689
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Foxo transcription factors have a conserved role in the adaptation of cells and organisms to nutrient and growth factor availability. Here we show that Foxo1 has a crucial, nonredundant role in T cells. In naive T cells, Foxo1 controlled the expression of the adhesion molecule L-selectin, the chemokine receptor CCR7 and the transcription factor Klf2, and its deletion was sufficient to alter lymphocyte trafficking. Furthermore, Foxo1 deficiency resulted in a severe defect in interleukin 7 receptor alpha-chain (IL-7R alpha) expression associated with its ability to bind an Il7r enhancer. Finally, growth factor withdrawal induced a Foxo1-dependent increase in Sell, Klf2 and Il7r expression. These data suggest that Foxo1 regulates the homeostasis and life span of naive T cells by sensing growth factor availability and regulating homing and survival signals.
引用
收藏
页码:176 / 184
页数:9
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