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

نویسندگان

  • Mohammad Haque
  • Jianyong Song
  • Kristin Fino
  • Youfei Wang
  • Praneet Sandhu
  • Xinmeng Song
  • Christopher Norbury
  • Bing Ni
  • Deyu Fang
  • Shahram Salek-Ardakani
  • Jianxun Song
چکیده

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 Cd28(-/-) or Ox40(-/-) 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 downstream molecule of NF-κB 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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عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2016