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

被引:130
作者
Lazarevic, Vanja [1 ]
Zullo, Alfred J. [1 ]
Schweitzer, Michelle N. [1 ]
Staton, Tracy L. [1 ]
Gallo, Elena M. [2 ,3 ]
Crabtree, Gerald R. [2 ,3 ]
Glimcher, Laurie H. [1 ,4 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[2] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Pathol, Stanford, CA 94305 USA
[4] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
IMMEDIATE-EARLY GENE; CUTTING EDGE; THYMOCYTE DEVELOPMENT; NEGATIVE SELECTION; FACTOR EGR-1; NKT CELLS; DIFFERENTIATION; DEFICIENT; REGULATORS; MICE;
D O I
10.1038/ni.1696
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:306 / 313
页数:8
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