细胞生物学
细胞毒性T细胞
T细胞
生物
T细胞受体
CD8型
细胞分化
CD28
刺激
人口
效应器
抗原提呈细胞
抗原
分子生物学
体外
免疫学
神经科学
免疫系统
基因
生物化学
医学
环境卫生
作者
Benjamin D. Hale,Yannik Severin,Fabienne Gräbnitz,Dominique Stark,Daniel Guignard,Julien Mena,Yasmin Festl,Sohyon Lee,Jacob Hanimann,Nathan Zangger,Michelle Meier,David Goslings,Olga Lamprecht,Beat M. Frey,Annette Oxenius,Berend Snijder
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2024-06-06
卷期号:384 (6700)
被引量:1
标识
DOI:10.1126/science.adh8967
摘要
After antigen stimulation, naïve T cells display reproducible population-level responses, which arise from individual T cells pursuing specific differentiation trajectories. However, cell-intrinsic predeterminants controlling these single-cell decisions remain enigmatic. We found that the subcellular architectures of naïve CD8 T cells, defined by the presence (T Ø ) or absence (T O ) of nuclear envelope invaginations, changed with maturation, activation, and differentiation. Upon T cell receptor (TCR) stimulation, naïve T Ø cells displayed increased expression of the early-response gene Nr4a1 , dependent upon heightened calcium entry. Subsequently, in vitro differentiation revealed that T Ø cells generated effector-like cells more so compared with T O cells, which proliferated less and preferentially adopted a memory-precursor phenotype. These data suggest that cellular architecture may be a predeterminant of naïve CD8 T cell fate.
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