Interleukin 2 plays a central role in Th2 differentiation

被引:320
作者
Cote-Sierra, J
Foucras, G
Guo, LY
Chiodetti, L
Young, HA
Hu-Li, J
Zhu, JF
Paul, WE
机构
[1] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
[2] NIAID, Cellular & Mol Immunol Lab, NIH, Bethesda, MD 20892 USA
[3] NCI, Expt Immunol Lab, Ctr Canc Res, Frederick, MD 21702 USA
关键词
D O I
10.1073/pnas.0400339101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Differentiation of naive CD4T cells into T helper (Th)2 cells requires signaling through the T cell receptor and an appropriate cytokine environment. IL-4 is critical for such Th2 differentiation. We show that IL-2 plays a central role in this process. The effect of IL-2 on Th2 generation does not depend on its cell growth or survival effects. Stat5a(-/-) cells show diminished differentiation to IL-4 production, and forced expression of a constitutively active form of Stat5a replaces the need for IL-2. In vivo IL-2 neutralization inhibits IL-4 production in two models. Studies of restriction enzyme accessibility and binding of Stat5 to chromatin indicate that IL-2 mediates its effect by stabilizing the accessibility of the 1/4 gene. Thus, IL-2 plays a critical role in the polarization of naive CD4T cells to the Th2 phenotype.
引用
收藏
页码:3880 / 3885
页数:6
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