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辅助性T细胞2作为初始T细胞分化为辅助性T细胞9的中间体,与Smad3/Smad4和干扰素调节因子4信号通路相关。

Th2 cells as an intermediate for the differentiation of naïve T cells into Th9 cells, associated with the Smad3/Smad4 and IRF4 pathway.

作者信息

Abdelaziz Mohamed Hamed, Wang Huixuan, Cheng Jianjun, Xu Huaxi

机构信息

Department of Immunology, School of Medicine, Jiangsu University, Zhenjiang, Jiangsu 212013, P.R. China.

Department of Laboratory Medicine, the Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu 212001, P.R. China.

出版信息

Exp Ther Med. 2020 Mar;19(3):1947-1954. doi: 10.3892/etm.2020.8420. Epub 2020 Jan 3.

Abstract

Type 9 T-helper (Th9) cells are associated with atopic and inflammatory diseases. Their increased levels and functions contribute to a number of inflammatory disorders, where they are accompanied by enhanced Th2-cell activity. However, there is currently no consensus regarding the association between Th9 and Th2 cells. Th9 cells may be induced from naïve T (Th0) cells under specific polarization conditions , a process driven by the addition of specific cytokines. In the present study, Th0 cells were cultured under Th9-polarizing conditions to promote differentiation into interleukin (IL)-4 IL-9 or IL-4 IL-9 T cells after 3 or 5 days in culture, respectively; the mRNA expression levels of IL-9 and IL-4 were consistent with the induced cell types. Simultaneously, the levels of interferon-regulatory factor 4 (IRF-4) and Smad3/Smad4 were significantly increased following Th9-cell polarization. It was therefore proposed that Th2 cells may be generated in the early stages of Th9-cell differentiation, and then ultimately differentiate into Th9 cells via the Smad3/Smad4 and IRF-4 activation pathway.

摘要

9型辅助性T(Th9)细胞与特应性和炎症性疾病相关。它们水平和功能的增加会导致多种炎症性疾病,这些疾病伴有Th2细胞活性增强。然而,目前关于Th9细胞与Th2细胞之间的关联尚无共识。Th9细胞可能在特定极化条件下由初始T(Th0)细胞诱导产生,这一过程由添加特定细胞因子驱动。在本研究中,将Th0细胞在Th9极化条件下培养,分别在培养3天或5天后促进其分化为白细胞介素(IL)-4 IL-9或IL-4 IL-9 T细胞;IL-9和IL-4的mRNA表达水平与诱导的细胞类型一致。同时,Th9细胞极化后,干扰素调节因子4(IRF-4)以及Smad3/Smad4的水平显著升高。因此有人提出,Th2细胞可能在Th9细胞分化的早期阶段产生,然后最终通过Smad3/Smad4和IRF-4激活途径分化为Th9细胞。

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