共 44 条
miR-150-Mediated Foxo1 Regulation Programs CD8+ T Cell Differentiation
被引:34
作者:
Ban, Young Ho
[1
]
Oh, Se-Chan
[2
,3
]
Seo, Sang-Hwan
[2
]
Kim, Seok-Min
[2
,3
]
Choi, In-Pyo
[2
,3
]
Greenberg, Philip D.
[4
]
Chang, Jun
[5
]
Kim, Tae-Don
[2
,3
]
Ha, Sang-Jun
[1
]
机构:
[1] Yonsei Univ, Dept Biochem, Coll Life Sci & Biotechnol, Seoul 03722, South Korea
[2] Korea Res Inst Biosci & Biotechnol, Immunotherapy Convergence Res Ctr, Daejeon 34141, South Korea
[3] Korea Univ Sci & Technol UST, Dept Funct Genom, KRIBB Sch Biosci, Daejeon, South Korea
[4] Univ Washington, Fred Hutchinson Canc Res Ctr, Seattle, WA 98195 USA
[5] Ewha Womans Univ, Div Life & Pharmaceut Sci, Ctr Cell Signaling & Drug Discovery Res, Seoul 03760, South Korea
来源:
CELL REPORTS
|
2017年
/
20卷
/
11期
基金:
新加坡国家研究基金会;
关键词:
TRANSCRIPTION FACTOR;
VIRAL-INFECTION;
CBL-B;
EFFECTOR;
MIR-150;
EXPRESSION;
RESPONSES;
NAIVE;
BET;
HOMEOSTASIS;
D O I:
10.1016/j.celrep.2017.08.065
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
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.
引用
收藏
页码:2598 / 2611
页数:14
相关论文