Regulation of T-cell tolerance by calcium/NFAT signaling

被引:67
作者
Baine, Ian [1 ]
Abe, Brian T. [1 ]
Macian, Fernando [1 ]
机构
[1] Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10461 USA
基金
美国国家卫生研究院;
关键词
T cells; anergy; signal transduction; transcription factors; NFAT; E3 UBIQUITIN LIGASE; CHROMATIN REMODELING COMPLEXES; TRANSCRIPTION FACTOR NFAT1; DNA-BINDING PROTEINS; CALCINEURIN A-ALPHA; ATP-DEFICIENT MICE; CASEIN KINASE-I; CBL-B; GENE-EXPRESSION; C-CBL;
D O I
10.1111/j.1600-065X.2009.00817.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Cells that escape negative selection in the thymus must be inactivated or eliminated in the periphery through a series of mechanisms that include the induction of anergy, dominant suppression by regulatory T cells, and peripheral deletion of self-reactive T cells. Calcium signaling plays a central role in the induction of anergy in T cells, which become functionally inactivated and incapable of proliferating and expressing cytokines following antigen re-encounter. Suboptimal stimulation of T cells results in the activation of a calcium/calcineurin/nuclear factor of activated T cells-dependent cell-intrinsic program of self-inactivation. The proteins encoded by those genes are required to impose a state of functional unresponsiveness through different mechanisms that include downregulation of T-cell receptor signaling and inhibition of cytokine transcription.
引用
收藏
页码:225 / 240
页数:16
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