Pre-TCR signaling regulates IL-7 receptor α expression promoting thymocyte survival at the transition from the double-negative to double-positive stage

被引:46
|
作者
Trigueros, C
Hozumi, K
Silva-Santos, B
Bruno, L
Hayday, AC
Owen, MJ
Pennington, DJ [1 ]
机构
[1] Guys Hosp, Guys Kings St Thomas Med Sch, Peter Gorer Dept Immunobiol, London SE1 9RT, England
[2] Canc Res UK, Lab Lymphocyte Mol Biol, London, England
[3] Natl Inst Med Res, London NW7 1AA, England
[4] Tokai Univ, Sch Med, Dept Immunol, Isehara, Kanagawa 25911, Japan
[5] Canc Res UK, Ctr Cell & Mol Biol, London, England
[6] GlaxoSmithKline, Med Res Ctr, Stevenage, Herts, England
关键词
IL-7; receptor; pre-TCR; proliferation; survival;
D O I
10.1002/eji.200323831
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The pre-T cell receptor (pre-TCR) and IL-7 receptor (IL-7R) are critical mediators of survival, proliferation and differentiation in immature thymocytes. Here we show that pre-TCR signaling directly maintains IL-7alpha expression as developing thymocytes undergo beta-selection. Inhibition of IL-7/IL-7R signaling in (CD44(-)CD25(-)) DN4 cells results in decreased generation of double-positive thymocytes due to increased death of rapidly proliferating P-selected cells. Thus, we identify a mechanism by which pre-TCR signaling controls the selective survival of TCRbeta(+) thymocytes, and define a further stage of T cell differentiation in which signaling from a TCR regulates the ability of that cell to respond to cytokine.
引用
收藏
页码:1968 / 1977
页数:10
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