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Cutting Edge: Generation of Memory Precursors and Functional Memory CD8+ T Cells Depends on T Cell Factor-1 and Lymphoid Enhancer-Binding Factor-1
被引:87
|作者:
Zhou, Xinyuan
[1
,2
]
Xue, Hai-Hui
[1
,3
]
机构:
[1] Univ Iowa, Dept Microbiol, Carver Coll Med, Iowa City, IA 52242 USA
[2] Third Mil Med Univ, Dept Immunol, Chongqing 400038, Peoples R China
[3] Univ Iowa, Interdisciplinary Immunol Grad Program, Carver Coll Med, Iowa City, IA 52242 USA
基金:
美国国家卫生研究院;
关键词:
WNT SIGNALING PATHWAY;
DIFFERENTIATION;
EFFECTOR;
EXPRESSION;
TCF-1;
ACTIVATION;
INFECTION;
FATES;
BET;
D O I:
10.4049/jimmunol.1201150
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
T cell factor (TCF)-1 and lymphoid enhancer-binding factor (LEF)-1 transcription factors have redundant roles in promoting thymocyte maturation. TCF-1 has been recently shown to critically regulate memory CD8(+) T cell differentiation and persistence. The complete spectra of regulatory roles for TCF-1 and LEF-1 in CD8(+) T cell responses are yet unknown. We conditionally targeted LEF-1, and by combination with germline deletion of TCF-1, we found that loss of both factors completely abrogated the generation of KLR G1(lo)IL-7R alpha(+) memory precursors in effector CD8(+) T cell populations in response to Listeria monocytogenes infection. Whereas CD8(+) effectors deficient for TCF-1 and LEF-1 retained the capacity to express IFN-gamma, granzyme B, and perforin, they were defective in TNF-alpha production. In the memory phase, the Ag-specific CD8(+) T cells lacking TCF-1 and LEF-1 exhibited an effector phenotype and were severely impaired in secondary expansion upon rechallenge. Thus, TCF-1 and LEF-1 cooperatively regulate generation of memory precursors and protective memory CD8(+) T cells. The Journal of Immunology, 2012, 189: 2722-2726.
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页码:2722 / 2726
页数:5
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