Blimp-1 attenuates Th1 differentiation by repression of ifng, tbx21, and bc16 gene expression

被引:114
作者
Cimmino, Luisa [4 ]
Martins, Gislaine A. [3 ]
Liao, Jerry [3 ]
Magnusdottir, Erna [2 ]
Grunig, Gabriele [3 ]
Perez, Rocio K. [2 ]
Calame, Kathryn L. [1 ,4 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Biol Sci, New York, NY 10032 USA
[3] Columbia Univ, Coll Phys & Surg, Dept Microbiol, New York, NY 10032 USA
[4] Columbia Univ, Coll Phys & Surg, Inst Human Nutr, New York, NY 10032 USA
关键词
D O I
10.4049/jimmunol.181.4.2338
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell-specific deletion of Blimp-1 causes abnormal T cell homeostasis and function, leading to spontaneous, fatal colitis in mice. Herein we explore the role of Blimp-1 in Th1/Th2 differentiation. Blimp-1 mRNA and protein are more highly expressed in Th2 cells compared with Th1 cells, and Blimp-1 attenuates IFN-gamma production in CD4 cells activated under nonpolarizing conditions. Although Blimp-1-deficient T cells differentiate normally to Th2 cytokines in vitro, Blimp-1 is required in vivo for normal Th2 Immoral responses to NP-KLH (4-hydroxy-3-nitrophenylacetyl/keyhole lymphocyte hemocyanin) immunization. Lack of Blimp-1 in CD4 T cells causes increased IFN-gamma, T-bet, and Bcl-6 mRNA. By chromatin immunoprecipitation we show that Blimp-1 binds directly to a distal regulatory region in the ifng gene and at multiple sites in tbx21 and bcl6 genes. Our data provide evidence that Blimp-1 functions in Th2 cells to reinforce Th2 differentiation by repressing critical Th1 genes.
引用
收藏
页码:2338 / 2347
页数:10
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