Department of Medicine, University of California San Diego, La Jolla, CA.
Department of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA.
J Immunol. 2023 Jul 15;211(2):241-251. doi: 10.4049/jimmunol.2200778.
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.
RNA 结合蛋白 DEAD -box 蛋白 5 (DDX5) 是基因表达的多功能调节剂,但它在 CD8+T 细胞生物学中的作用尚未得到广泛研究。在这项研究中,我们证明了在小鼠 CD8+T 细胞中缺失 DDX5 会减少终末效应、效应记忆 T 和终末效应记忆细胞的分化,同时增加中央记忆 T 细胞的生成,而强制表达 DDX5 则会产生相反的表型。DDX5 缺陷型 CD8+T 细胞表现出促进中央记忆 T 细胞分化的基因表达增加,包括 Tcf7 和 Eomes。综上所述,这些发现揭示了 DDX5 在调节效应器和记忆 CD8+T 细胞亚群对微生物感染的反应中的作用。