Andersson U, Sander B, Andersson J, Möller G
Department of Immunology, Stockholm University, Sweden.
Eur J Immunol. 1988 Dec;18(12):2081-4. doi: 10.1002/eji.1830181232.
The intracellular accumulation of five different lymphokines in individual cells could be identified by lymphokine-specific antibodies and an indirect immunofluorescence technique with UV microscopy. When peripheral blood mononuclear cells from one healthy donor were activated in vitro by the T cell mitogen anti-CD3 monoclonal antibody, the maximal number of cells producing interleukin (IL)2, IL 6 or tumor necrosis factor (TNF)-alpha occurred 6 h after initiation of the cultures, while peak numbers of interferon-gamma, TNF-beta and a second wave of TNF-alpha-synthesizing cells were noted approximately 20 h later. By performing two-color immunofluorescence studies we observed a variegated production pattern with cells making no, one or several lymphokines simultaneously. All five cytokines accumulated in the Golgi organelle resulting in a very characteristic morphology of the staining with or without additional cytoplasmic immunofluorescence.
通过淋巴因子特异性抗体和紫外线显微镜间接免疫荧光技术,可以识别单个细胞内五种不同淋巴因子的细胞内积累情况。当来自一名健康供体的外周血单个核细胞在体外被T细胞有丝分裂原抗CD3单克隆抗体激活时,产生白细胞介素(IL)-2、IL-6或肿瘤坏死因子(TNF)-α的细胞最大数量在培养开始后6小时出现,而干扰素-γ、TNF-β和第二波TNF-α合成细胞的峰值数量大约在20小时后出现。通过进行双色免疫荧光研究,我们观察到一种多样化的产生模式,细胞同时不产生、产生一种或几种淋巴因子。所有五种细胞因子都在高尔基体中积累,导致染色呈现出非常独特的形态,无论有无额外的细胞质免疫荧光。