Vi impacts on the cytokine profile of innate cells shortly after infection.
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Cells were stained with mAb to specific surface markers F4/80+, CD11c+, DX5+/CD3− and Ly6G+ to identify innate populations, permeabilised and stained with anti-MIP-2, TNF-α, IFN-γ, perforin and IL-6. Data represent percent of cytokine positive cells out of total spleen populations ± SEM.*indicates significant values of p**, p***, p†indicates significant values of p††, p†††, p+ are compared to Vi− infected mice.
采用针对特异性表面标志物F4/80+、CD11c+、DX5+/CD3−及Ly6G+的单克隆抗体(monoclonal antibody, mAb)对细胞进行染色,以鉴定先天免疫细胞群;随后对细胞进行透化处理,并用抗巨噬细胞炎症蛋白2(macrophage inflammatory protein 2, MIP-2)、肿瘤坏死因子α(Tumor Necrosis Factor α, TNF-α)、干扰素γ(Interferon γ, IFN-γ)、穿孔素及白细胞介素6(Interleukin 6, IL-6)的抗体实施胞内染色。数据以脾脏总细胞群中细胞因子阳性细胞所占百分比±标准误(standard error of the mean, SEM)表示。*代表p**、p***组具有统计学显著性,†代表p††、p†††组具有统计学显著性,所有比较均以Vi⁻感染小鼠为对照。



