miR-150-Mediated Foxo1 Regulation Programs CD8+ T Cell Differentiation.

نویسندگان

  • Young Ho Ban
  • Se-Chan Oh
  • Sang-Hwan Seo
  • Seok-Min Kim
  • In-Pyo Choi
  • Philip D Greenberg
  • Jun Chang
  • Tae-Don Kim
  • Sang-Jun Ha
چکیده

MicroRNA (miR)-150 is a developmental regulator of several immune-cell types, but its role in CD8+ T cells is largely unexplored. Here, we show that miR-150 regulates the generation of memory CD8+ T cells. After acute virus infection, miR-150 knockout (KO) mice exhibited an accelerated differentiation of CD8+ T cells into memory cells and improved production of effector cytokines. Additionally, miR-150 KO CD8+ T cells displayed an enhanced recall response and improved protection against infections with another virus and bacteria. We found that forkhead box O1 (Foxo1) and T cell-specific transcription factor 1 (TCF1) are upregulated during the early activation phase in miR-150 KO CD8+ T cells and that miR-150 directly targets and suppresses Foxo1. These results suggest that miR-150-mediated suppression of Foxo1 regulates the balance between effector and memory cell differentiation, which might aid in the development of improved vaccines and T cell therapeutics.

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عنوان ژورنال:
  • Cell reports

دوره 20 11  شماره 

صفحات  -

تاریخ انتشار 2017