Sander B, Höidén I, Andersson U, Möller E, Abrams J S
Department of Immunology, Arrhenius Laboratories for Natural Sciences, Stockholm University, Sweden.
J Immunol Methods. 1993 Dec 3;166(2):201-14. doi: 10.1016/0022-1759(93)90361-a.
Production of IL-2, IL-3, IL-4, IL-5, IL-6, IL-10, IFN-gamma, GM-CSF (granulocyte-macrophage colony stimulating factor) and macrophage colony stimulating factor by murine peripheral blood and spleen cells was analyzed following primary and secondary mitogen stimulation in vitro. Individual cytokine producing cells were detected by an intracytoplasmic staining technique. Cytokine production in cells from peripheral blood and spleen was comparable and more rapidly induced by calcium ionophore and phorbol 12-myristate 13-acetate than by concanavaling A. Restimulation in vitro induced both a swift production of cytokines and, for some cytokines, higher frequencies of producing cells. This was especially evident for IL-10 secreting cells, which increased 30-80 times in secondary responses. These analyses using the dual approaches of immunoenzymetric and fluorescent immunohistochemical techniques provide important evidence that cytokine induction kinetics can differ following primary or secondary stimulation.
在体外进行初次和二次丝裂原刺激后,分析了小鼠外周血和脾细胞产生白细胞介素-2(IL-2)、白细胞介素-3(IL-3)、白细胞介素-4(IL-4)、白细胞介素-5(IL-5)、白细胞介素-6(IL-6)、白细胞介素-10(IL-10)、γ干扰素(IFN-γ)、粒细胞-巨噬细胞集落刺激因子(GM-CSF)和巨噬细胞集落刺激因子的情况。通过胞内染色技术检测单个产生细胞因子的细胞。外周血和脾细胞中细胞因子的产生情况相当,钙离子载体和佛波醇12-肉豆蔻酸酯13-乙酸酯比刀豆球蛋白A能更快地诱导细胞因子产生。体外再次刺激既诱导了细胞因子的快速产生,对于某些细胞因子而言,也诱导了产生细胞的更高频率。这在分泌IL-10的细胞中尤为明显,其在二次反应中增加了30至80倍。这些采用免疫酶法和荧光免疫组织化学技术的双重方法进行的分析提供了重要证据,即初次或二次刺激后细胞因子诱导动力学可能不同。