效应器
CD8型
细胞毒性T细胞
生物
细胞生物学
基因表达
存储单元
细胞分化
表型
T细胞
基因
分子生物学
遗传学
抗原
体外
物理
免疫系统
量子力学
电压
晶体管
作者
Tiani L. Louis,William H. Wong,Priscilla Yao,Nadia Kurd,Tiffani Tysl,Cynthia S. Indralingam,Shengyun Ma,Wendy Huang,John T. Chang
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2023-06-02
卷期号:211 (2): 241-251
被引量:1
标识
DOI:10.4049/jimmunol.2200778
摘要
Abstract The RNA-binding protein DEAD-box protein 5 (DDX5) is a polyfunctional regulator of gene expression, but its role in CD8+ T cell biology has not been extensively investigated. In this study, we demonstrate that deletion of DDX5 in murine CD8+ T cells reduced the differentiation of terminal effector, effector memory T, and terminal effector memory cells while increasing the generation of central memory T cells, whereas forced expression of DDX5 elicited the opposite phenotype. DDX5-deficient CD8+ T cells exhibited increased expression of genes that promote central memory T cell differentiation, including Tcf7 and Eomes. Taken together, these findings reveal a role for DDX5 in regulating the differentiation of effector and memory CD8+ T cell subsets in response to microbial infection.
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