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      The gene encoding early growth response 2, a target of the transcription factor NFAT, is required for the development and maturation of natural killer T cells.

      Nature immunology
      Animals, CD4-Positive T-Lymphocytes, immunology, CD8-Positive T-Lymphocytes, Calcineurin, metabolism, Cell Differentiation, Cells, Cultured, Early Growth Response Protein 2, genetics, Humans, Mice, Mice, Inbred C57BL, Mice, Knockout, NFATC Transcription Factors, Natural Killer T-Cells

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          Abstract

          The influence of signals transmitted by the phosphatase calcineurin and the transcription factor NFAT on the development and function of natural killer T (NKT) cells is unclear. In this report, we demonstrate that the transcription factor early growth response 2 (Egr2), a target gene of NFAT, was specifically required for the ontogeny of NKT cells but not that of conventional CD4(+) or CD8(+) T cells. NKT cells developed normally in the absence of Egr1 or Egr3, which suggests that Egr2 is a specific regulator of NKT cell differentiation. We found that Egr2 was important in the selection, survival and maturation of NKT cells. Our findings emphasize the importance of the calcineurin-NFAT-Egr2 pathway in the development of the NKT lymphocyte lineage.

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