Cutting Edge: Ikaros Is a Regulator of Th2 Cell Differentiation

被引:58
作者
Quirion, Mary R. [1 ]
Gregory, Grepry D. [1 ]
Umetsu, Sarah E. [1 ]
Winandy, Susan [1 ]
Brown, Melissa A. [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Microbiol & Immunol, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
HELPER T-CELLS; CYTOKINE PRODUCTION; IL-4; GENE; HISTONE ACETYLATION; DNA-BINDING; EXPRESSION; BET; TRANSCRIPTION; COMMITMENT; INDUCTION;
D O I
10.4049/jimmunol.182.2.741
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ikaros, a hematopoietic transcription factor, has well defined effects on early lymphocyte development in the bone marrow and thymus. In this study we demonstrate that Ikaros is a positive regulator of Th2 cytokine gene expression in peripheral T cells. CD4(+) T cells from naive Ikaros(null) mice cultured under Th2-skewing conditions express the Th1 cytokine IFN-gamma and have reduced IL-4, IL-5, and IL-13 expression. Ikaros directly associates with several Th2 locus regulatory regions in naive CD4(+) T cells. The decreased ability to express Th2 cytokines in Ikaros(null) T cells corresponds with histone 3 hypoacetylation across the Th2 cytokine locus as well as decreased GATA3 and cMaf and increased T-bet and STAT1 expression. These data support a model whereby Ikaros directly activates Th2 gene expression by promoting local chromatin accessibility during CD4(+) T cell differentiation and also acts indirectly to regulate expression of Th2- and Th1-specific transcription factors. The Journal of Immunology, 2009, 182: 741-745.
引用
收藏
页码:741 / 745
页数:5
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