Modulation of chromatin structure regulates cytokine gene expression during T cell differentiation

被引:623
作者
Agarwal, S [1 ]
Rao, A [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Pathol, Ctr Blood Res, Boston, MA 02115 USA
关键词
D O I
10.1016/S1074-7613(00)80642-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Differentiating cells undergo programmed alterations in their patterns of gene expression, which are often regulated by structural changes in chromatin. Here we demonstrate that T cell differentiation results in long-range changes in the chromatin structure of effector cytokine genes, which persist in resting Th1 and Th2 cells in the absence of further stimulation. Differentiation of naive T helper cells into mature Th2 cells is associated with chromatin remodeling of the IL-4 and IL-13 genes, whereas differentiation into Th1 cells evokes remodeling of the IFN gamma but not IL-4 or IL-13 genes. IL-4 locus remodeling is accompanied by demethylation and requires both antigen stimulation and STAT6 activation. We propose that chromatin remodeling of cytokine gene loci is functionally associated with productive T cell differentiation and may explain the coordinate regulation of Th2 cytokine genes.
引用
收藏
页码:765 / 775
页数:11
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