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Article
Nature Immunology  2, 316 - 324 (2001)
Published online: April 2001; Corrected online: 06 February 2008 | doi:10.1038/86318


There is a Corrigendum (March 2008) associated with this Article.

Gene regulation mediated by calcium signals in T lymphocytes

Stefan Feske1, Jena Giltnane2, Ricardo Dolmetsch3, Louis M. Staudt2 & Anjana Rao1

1  Center for Blood Research and Department of Pathology, Harvard Medical School, Boston, MA 02115, USA.

2  Metabolism Branch, Division of Clinical Sciences, National Cancer Institute, Bethesda, MD 20892, USA.

3  Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.

Correspondence should be addressed to Anjana Rao arao@cbr.med.harvard.edu
NOTE: In the version of the article initially published, many errors and inappropriate manipulations were made in Figures 1, 3 and 5 (see PDF for details).

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.

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Nature Immunology
ISSN: 1529-2908
EISSN: 1529-2916
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