Gene regulation mediated by calcium signals in T lymphocytes

被引:480
作者
Feske, S
Giltnane, J
Dolmetsch, R
Staudt, LM
Rao, A [1 ]
机构
[1] Harvard Univ, Sch Med, Ctr Blood Res, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Childrens Hosp, Dept Pathol, Boston, MA 02115 USA
[3] NCI, Metab Branch, Div Clin Sci, Bethesda, MD 20892 USA
关键词
D O I
10.1038/86318
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Modulation of many signaling pathways in antigen-stimulated T and B cells results in global changes in gene expression. Here we investigate the contribution of calcium signaling to gene expression in T cells using cell lines from two severe-combined immunodeficiency patients with several cytokine deficiencies and diminished activation of the transcription factor NFAT nuclear factor of activated T cells. These T cells show a strong defect in transmembrane calcium influx that is also apparent in their B cells and fibroblasts. DNA microarray analysis of calcium entry-deficient and control T cells shows that Ca2+ signals both activate and repress gene expression and are largely transduced through the phosphatase calcineurin. We demonstrate an elaborate network of signaling pathways downstream of the T cell receptor, explaining the complexity of changes in gene expression during T cell activation.
引用
收藏
页码:316 / 324
页数:9
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