Identification of lineage-specifying cytokines that signal all CD8+-cytotoxic-lineage-fate 'decisions' in the thymus

被引:25
作者
Etzensperger, Ruth [1 ]
Kadakia, Tejas [1 ]
Tai, Xuguang [1 ]
Alag, Amala [1 ]
Guinter, Terry I. [1 ]
Egawa, Takeshi [2 ]
Erman, Batu [3 ]
Singer, Alfred [1 ]
机构
[1] NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USA
[2] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[3] Sabanci Univ, Fac Engn & Nat Sci, Mol Biol Genet & Bioengn Program, Istanbul, Turkey
基金
美国国家卫生研究院;
关键词
T-CELL LINEAGE; TGF-BETA; STROMAL LYMPHOPOIETIN; TRANSCRIPTION FACTORS; RUNX PROTEINS; DIFFERENTIATION; THYMOCYTES; EXPRESSION; PROMOTES; CD4;
D O I
10.1038/ni.3847
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 antigen receptor (TCR) signaling in the thymus initiates positive selection, but the CD8(+)-lineage fate is thought to be induced by cytokines after TCR signaling has ceased, although this remains controversial and unproven. We have identified four cytokines (IL-6, IFN-gamma, TSLP and TGF-beta) that did not signal via the common gamma-chain (gamma(c)) receptor but that, like IL-7 and IL-15, induced expression of the lineage-specifying transcription factor Runx3d and signaled the generation of CD8(+) T cells. Elimination of in vivo signaling by all six of these 'lineage-specifying cytokines' during positive selection eliminated Runx3d expression and completely abolished the generation of CD8(+) single-positive thymocytes. Thus, this study proves that signaling during positive selection by lineage-specifying cytokines is responsible for all CD8(+)-lineage-fate 'decisions' in the thymus.
引用
收藏
页码:1218 / +
页数:15
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