共 47 条
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.
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页码:306 / 313
页数:8
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