Zhuang Yonghua, Huang Zan, Nishida Jun, Brown Melissa, Zhang Lin, Huang Hua
Division of Allergy and Immunology, Department of Medicine, National Jewish Health, Denver, CO, USA.
Immunology. 2009 Sep;128(1):34-42. doi: 10.1111/j.1365-2567.2009.03049.x.
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.
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。