miR-150-mediated Foxo1 regulation programs CD8+ T cell differentiation

Cited 37 time in scopus
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Title
miR-150-mediated Foxo1 regulation programs CD8+ T cell differentiation
Author(s)
Y H Ban; Se-Chan Oh; Sang-Hwan Seo; Seok-Min Kim; In Pyo Choi; P D Greenberg; J Chang; Tae-Don Kim; S J Ha
Bibliographic Citation
Cell Reports, vol. 20, no. 11, pp. 2598-2611
Publication Year
2017
Abstract
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
Keyword
acuteCD8differentiationFoxo1infectionLCMVmemorymiR-150primary immune responserecall
ISSN
2211-1247
Publisher
Elsevier-Cell Press
Full Text Link
http://dx.doi.org/10.1016/j.celrep.2017.08.065
Type
Article
Appears in Collections:
Division of A.I. & Biomedical Research > Immunotherapy Research Center > 1. Journal Articles
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