首页> 外文期刊>Cell Research >GATA-3 promotes Th2 responses through three different mechanisms: induction of Th2 cytokine production, selective growth of Th2 cells and inhibition of Th1 cell-specific factors.
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GATA-3 promotes Th2 responses through three different mechanisms: induction of Th2 cytokine production, selective growth of Th2 cells and inhibition of Th1 cell-specific factors.

机译:GATA-3通过三种不同的机制促进Th2反应:诱导Th2细胞因子产生,Th2细胞的选择性生长以及Th1细胞特异性因子的抑制。

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摘要

Naive CD4 T cells can differentiate into at least two different types of T helpers, Th1 and Th2 cells. Th2 cells, capable of producing IL-4, IL-5 and IL-13, are involved in humoral immunity against extracellular pathogens and in the induction of asthma and other allergic diseases. In this review, we summarize recent reports regarding the transcription factors involved in Th2 differentiation and cell expansion, including Stat5, Gfi-1 and GATA-3. Stat5 activation is necessary and sufficient for IL-2-mediated function in Th2 differentiation. Enhanced Stat5 signaling induces Th2 differentiation independent of IL-4 signaling; although it does not up-regulate GATA-3 expression, it does require the presence of GATA-3 for its action. Gfi-1, induced by IL-4, promotes the expansion of GATA-3-expressing cells. Analysis of conditional Gata3 knockout mice confirmed the critical role of GATA-3 in Th2 cell differentiation (both IL-4 dependent and IL-4 independent) and in Th2 cell proliferation and also showed the importance of basal GATA-3 expression in inhibiting Th1 differentiation.Cell Research (2006) 16: 3-10. doi:10.1038/sj.cr.7310002; published online 16 January 2006.
机译:原始CD4 T细胞可以分化为至少两种不同类型的T辅助细胞,即Th1和Th2细胞。能够产生IL-4,IL-5和IL-13的Th2细胞参与针对细胞外病原体的体液免疫以及哮喘和其他过敏性疾病的诱导。在这篇综述中,我们总结了有关Th2分化和细胞扩增所涉及的转录因子的最新报道,包括Stat5,Gfi-1和GATA-3。 Stat5激活对于Th-2分化中IL-2介导的功能是必要和充分的。增强的Stat5信号传导诱导Th2分化,独立于IL-4信号传导;尽管它不上调GATA-3的表达,但它确实需要GATA-3的存在才能发挥作用。由IL-4诱导的Gfi-1促进表达GATA-3的细胞的扩增。对条件性Gata3基因敲除小鼠的分析证实了GATA-3在Th2细胞分化(IL-4依赖性和IL-4依赖性)以及Th2细胞增殖中的关键作用,并且还显示了基础GATA-3表达在抑制Th1分化中的重要性细胞研究(2006)16:3-10。 doi:10.1038 / sj.cr.7310002;在线发布于2006年1月16日。

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