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持续表达T-bet对于沉默1型辅助性T细胞中产生白细胞介素-4的潜能是必需的。

A continuous T-bet expression is required to silence the interleukin-4-producing potential in T helper type 1 cells.

作者信息

Zhuang Yonghua, Huang Zan, Nishida Jun, Brown Melissa, Zhang Lin, Huang Hua

机构信息

Division of Allergy and Immunology, Department of Medicine, National Jewish Health, Denver, CO, USA.

出版信息

Immunology. 2009 Sep;128(1):34-42. doi: 10.1111/j.1365-2567.2009.03049.x.

Abstract

To develop into committed T helper type 1 (Th1) cells, naive CD4(+) T cells not only need to acquire the capacity to produce interferon-gamma (IFN-gamma), but they also need to gain the ability to silence their interleukin-4 (IL-4) -producing potential. How Th1 cells silence their Th2 cytokine-producing potential is an important yet unresolved issue in Th1 immunity. We found that a lack of IL-4 stimulation was not sufficient to silence the IL-4-producing potential in activated CD4(+) T cells and that Th1-promoting factor was required. Although it has been shown that T-bet is a crucial factor in suppressing Il4 gene expression, it is unclear whether a continuous presence of T-bet is required to silence the Il4 gene in Th1 cells. To address this problem, we used an inducible form of T-bet - a T-bet-oestrogen receptor fusion molecule (T-bet-ER). We found that the activation of T-bet during primary or secondary culture was sufficient to silence IL-4-producing potential. On the other hand, the inactivation of T-bet after naïve CD4(+) T cells had differentiated into Th1 cells resulted in derepression of Il4 gene transcription. Additionally, we found that T-bet is required to maintain Ifng expression. Our data demonstrate that the continuous expression of T-bet is required for Th1 cells to silence their IL-4-producing potential.

摘要

为了发育成为定型的1型辅助性T细胞(Th1细胞),初始CD4(+) T细胞不仅需要获得产生γ干扰素(IFN-γ)的能力,还需要获得抑制其产生白细胞介素-4(IL-4)的能力。Th1细胞如何抑制其产生Th2细胞因子的能力是Th1免疫中一个重要但尚未解决的问题。我们发现,缺乏IL-4刺激不足以抑制活化的CD4(+) T细胞产生IL-4的能力,还需要Th1促进因子。虽然已经表明T-bet是抑制Il4基因表达的关键因素,但尚不清楚在Th1细胞中是否需要持续存在T-bet来沉默Il4基因。为了解决这个问题,我们使用了一种可诱导形式的T-bet——T-bet-雌激素受体融合分子(T-bet-ER)。我们发现,在原代或传代培养过程中激活T-bet足以抑制产生IL-4的能力。另一方面,在初始CD4(+) T细胞分化为Th1细胞后使T-bet失活会导致Il4基因转录的去抑制。此外,我们发现维持Ifng表达需要T-bet。我们的数据表明,Th1细胞抑制其产生IL-4的能力需要T-bet的持续表达。

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