C-Myc regulation by costimulatory signals modulates the generation of CD8+ memory T cells during viral infection

被引:20
|
作者
Haque, Mohammad [1 ]
Song, Jianyong [2 ]
Fino, Kristin [1 ]
Wang, Youfei [2 ]
Sandhu, Praneet [1 ]
Song, Xinmeng [1 ]
Norbury, Christopher [1 ]
Ni, Bing [2 ]
Fang, Deyu [3 ]
Salek-Ardakani, Shahram [4 ]
Song, Jianxun [1 ]
机构
[1] Penn State Univ, Coll Med, Dept Microbiol & Immunol, Hershey, PA USA
[2] Third Mil Med Univ, Inst Irradiat Immunol, Chongqing, Peoples R China
[3] Northwestern Univ, Feinberg Sch Med, Dept Pathol, Chicago, IL 60611 USA
[4] Univ Florida, Dept Pathol Immunol & Lab Med, Gainesville, FL USA
来源
OPEN BIOLOGY | 2016年 / 6卷 / 01期
关键词
c-Myc; costimulation; CD8(+) T cells; memory; viral infection; CD28; COSTIMULATION; BREAST-CANCER; SELF-RENEWAL; STEM-CELLS; OX40; DIFFERENTIATION; TRANSCRIPTION; SURVIVIN; EXPRESSION; EFFECTOR;
D O I
10.1098/rsob.150208
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The signalling mechanisms of costimulation in the development of memory T cells remain to be clarified. Here, we show that the transcription factor c-Myc in CD8(+) T cells is controlled by costimulatory molecules, which modulates the development of memory CD8(+) T cells. C-Myc expression was dramatically reduced in Cd282/2 or Ox402/2 memory CD8(+) T cells, and c-Myc over-expression substantially reversed the defects in the development of T-cell memory following viral infection. C-Myc regulated the expression of survivin, an inhibitor of apoptosis, which promoted the generation of virus-specific memory CD8(+) T cells. Moreover, over-expression of survivin with bcl-xL, a downstreammolecule of NF-kappa B and intracellular target of costimulation that controls survival, in Cd28(-/-) or Ox40(-/-) CD8(+) T cells, reversed the defects in the generation of memory T cells in response to viral infection. These results identify c-Myc as a key controller of memory CD8(+) T cells from costimulatory signals.
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页数:13
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