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小鼠产生粒细胞-巨噬细胞集落刺激因子(GM-CSF)的辅助性T细胞(THGM)的体外分化

In Vitro Differentiation of Mouse Granulocyte-macrophage-colony-stimulating Factor (GM-CSF)-producing T Helper (THGM) Cells.

作者信息

Lu Yi, Fu Xin-Yuan, Zhang Yongliang

机构信息

Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore; Immunology Programme, Life Sciences Institute, National University of Singapore; Cancer Science Institute of Singapore, Yong Loo Lin School of Medicine, National University of Singapore.

Cancer Science Institute of Singapore, Yong Loo Lin School of Medicine, National University of Singapore.

出版信息

J Vis Exp. 2018 Sep 10(139):58087. doi: 10.3791/58087.

Abstract

The granulocyte-macrophage-colony-stimulating factor (GM-CSF)-producing T helper (THGM) cell is a newly identified T helper cell subset that predominantly secretes GM-CSF without producing interferon (IFN)γ or interleukin (IL)-17 and is found to play an essential role in the autoimmune neuroinflammation. A method of isolation of naive CD4+ T cells from a single-cell suspension of splenocytes and THGM cell generation from naive CD4+ T cells would be a useful technique in the study of T cell-mediated immunity and autoimmune diseases. Here we describe a method that differentiates mouse naive CD4+ T cells into THGM cells promoted by IL-7. The outcome of the differentiation was assessed by the analysis of the cytokines expression using different techniques, including intracellular cytokine staining combined with flow cytometry, a quantitative real-time polymerase chain reaction (PCR), and enzyme-linked immunosorbent assays (ELISA). Using the THGM differentiation protocol as described here, about 55% of the cells expressed GM-CSF with a minimal expression of IFNα or IL-17. The predominant expression of GM-CSF by THGM cells was further confirmed by the analysis of the expression of GM-CSF, IFNα, and IL-17 at both mRNA and protein levels. Thus, this method can be used to differentiate naive CD4+ T cells to THGM cells in vitro, which will be useful in the study of THGM cell biology.

摘要

产生粒细胞-巨噬细胞集落刺激因子(GM-CSF)的辅助性T(THGM)细胞是一种新发现的辅助性T细胞亚群,主要分泌GM-CSF,不产生干扰素(IFN)γ或白细胞介素(IL)-17,并且发现在自身免疫性神经炎症中起重要作用。从脾细胞单细胞悬液中分离初始CD4⁺T细胞以及从初始CD4⁺T细胞生成THGM细胞的方法,在研究T细胞介导的免疫和自身免疫性疾病中将是一项有用的技术。在此,我们描述一种通过白细胞介素-7促进将小鼠初始CD4⁺T细胞分化为THGM细胞的方法。使用包括细胞内细胞因子染色结合流式细胞术、定量实时聚合酶链反应(PCR)和酶联免疫吸附测定(ELISA)在内的不同技术,通过分析细胞因子表达来评估分化结果。使用此处所述的THGM分化方案,约55%的细胞表达GM-CSF,而IFNα或IL-17的表达极少。通过在mRNA和蛋白质水平分析GM-CSF、IFNα和IL-17的表达,进一步证实了THGM细胞中GM-CSF的主要表达。因此,该方法可用于在体外将初始CD4⁺T细胞分化为THGM细胞,这将有助于THGM细胞生物学的研究。

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