蛋白激酶B
mTORC1型
细胞生物学
效应器
PI3K/AKT/mTOR通路
生物
细胞生长
T细胞
CD8型
癌症研究
信号转导
免疫学
免疫系统
生物化学
作者
Leena Abdullah,L. Benjamin Hills,Evan B. Winter,Yina H. Huang
出处
期刊:Immunometabolism
[Hapres]
日期:2021-01-01
卷期号:3 (1)
被引量:32
标识
DOI:10.20900/immunometab20210007
摘要
Abstract Akt kinases translate various external cues into intracellular signals that control cell survival, proliferation, metabolism and differentiation. This review discusses the requirement for Akt and its targets in determining the fate and function of T cells. We discuss the importance of Akt at various stages of T cell development including β-selection during which Akt fulfills the energy requirements of highly proliferative DN3 cells. Akt also plays an integral role in CD8 T cell biology where its regulation of Foxo transcription factors and mTORC1 metabolic activity controls effector versus memory CD8 T cell differentiation. Finally, Akt promotes the differentiation of naïve CD4 T cells into Th1, Th17 and Tfh cells but inhibits the development of Treg cells. We also highlight how modulating Akt in T cells is a promising avenue for enhancing cell-based cancer immunotherapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI