Lu Yi, Fu Xin-Yuan, Zhang Yongliang
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.
J Vis Exp. 2018 Sep 10(139):58087. doi: 10.3791/58087.
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.
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。