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Immunity. 2010 Aug 27;33(2):229-40. doi: 10.1016/j.immuni.2010.08.002.

Differentiation and persistence of memory CD8(+) T cells depend on T cell factor 1.

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1
Department of Microbiology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.

Abstract

T cell factor 1 (TCF-1) is a transcription factor known to act downstream of the canonical Wnt pathway and is essential for normal T cell development. However, its physiological roles in mature CD8(+) T cell responses are unknown. Here we showed that TCF-1 deficiency limited proliferation of CD8(+) effector T cells and impaired their differentiation toward a central memory phenotype. Moreover, TCF-1-deficient memory CD8(+) T cells were progressively lost over time, exhibiting reduced expression of the antiapoptotic molecule Bcl-2 and interleukin-2 receptor beta chain and diminished IL-15-driven proliferation. TCF-1 was directly associated with the Eomes allele and the Wnt-TCF-1 pathway was necessary and sufficient for optimal Eomes expression in naive and memory CD8(+) T cells. Importantly, forced expression of Eomes partly protected TCF-1-deficient memory CD8(+) T cells from time-dependent attrition. Our studies thus identify TCF-1 as a critical player in a transcriptional program that regulates memory CD8 differentiation and longevity.

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PMID:
20727791
PMCID:
PMC2928475
DOI:
10.1016/j.immuni.2010.08.002
[Indexed for MEDLINE]
Free PMC Article

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