Suppr超能文献

miR-150 介导的 Foxo1 调控程序 CD8 T 细胞分化。

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

机构信息

Department of Biochemistry, College of Life Science & Biotechnology, Yonsei University, Seoul 03722, Korea.

Immunotherapy Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 34141, Korea; Department of Functional Genomics, KRIBB School of Bioscience, Korea University of Science and Technology (UST), Daejeon, Korea.

出版信息

Cell Rep. 2017 Sep 12;20(11):2598-2611. doi: 10.1016/j.celrep.2017.08.065.

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.

摘要

miR-150 是几种免疫细胞类型的发育调节剂,但它在 CD8 T 细胞中的作用在很大程度上尚未被探索。在这里,我们表明 miR-150 调节记忆性 CD8 T 细胞的生成。在急性病毒感染后,miR-150 敲除 (KO) 小鼠表现出 CD8 T 细胞更快地分化为记忆细胞,并改善了效应细胞因子的产生。此外,miR-150 KO CD8 T 细胞表现出增强的回忆反应,并改善了对另一种病毒和细菌感染的保护。我们发现,在 miR-150 KO CD8 T 细胞的早期激活阶段,叉头框蛋白 O1 (Foxo1) 和 T 细胞特异性转录因子 1 (TCF1) 上调,并且 miR-150 直接靶向并抑制 Foxo1。这些结果表明,miR-150 介导的 Foxo1 抑制调节效应细胞和记忆细胞分化之间的平衡,这可能有助于开发改进的疫苗和 T 细胞治疗。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验