Friend of GATA-1 represses GATA-3-dependent activity in CD4+ T cells

被引:79
作者
Zhou, MX
Ouyang, W
Gong, Q
Katz, SG
White, JM
Orkin, SH
Murphy, KM
机构
[1] Washington Univ, Sch Med, Howard Hughes Med Inst, Dept Pathol & Immunol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Div Rheumatol, Dept Med, St Louis, MO 63110 USA
[3] Harvard Univ, Sch Med, Howard Hughes Med Inst, Childrens Hosp Med Ctr,Div Hematol Oncol, Boston, MA 02115 USA
关键词
GATA-3; FOG-1; thymocyte; T lymphocyte; cytokine;
D O I
10.1084/jem.194.10.1461
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 development of naive CD4(+) T cells into a T helper (Th) 2 subset capable of producing interleukin (IL)-4, IL-5, and IL-13 involves a signal transducer and activator of transcription (Stat)6-dependent induction of GATA-3 expression, followed by Stat6-independent GATA-3 autoactivation. The friend of GATA (FOG)-1 protein regulates GATA transcription factor activity in several stages of hematopoietic development including erythrocyte and megakaryocyte differentiation, but whether FOG-1 regulates GATA-3 in T cells is uncertain. We show that FOG-1 can repress GATA-3-dependent activation of the IL-5 promoter in T cells. Also, FOG-1 overexpression during primary activation of naive T cells inhibited Th2 development in CD4(+)-T cells. FOG-1 fully repressed GATA-3-dependent Th2 development and GATA-3 autoactivation, but not Stat6-dependent induction of GATA-3. FOG-1 overexpression repressed development of Th2 cells from naive T cells, but did not reverse the phenotype of fully committed Th2 cells. Thus, FOG-1 may be one factor capable of regulating the Th2 development.
引用
收藏
页码:1461 / 1471
页数:11
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