Horii Y, Muraguchi A, Suematsu S, Matsuda T, Yoshizaki K, Hirano T, Kishimoto T
Division of Immunology, School of Medicine, Osaka University, Japan.
J Immunol. 1988 Sep 1;141(5):1529-35.
Regulation of BSF-2/IL-6 production in peripheral mononuclear cells (MNC) was studied. BSF-2 mRNA expression in mitogen-stimulated MNC showed a biphasic response, the first peak around 4 h and the second peak around 48 h. This was caused by different kinetics of BSF-2 mRNA expression in distinct subpopulations of MNC; M phi expressed BSF-2 mRNA at 5 h in the absence of any stimulation, and mitogen-stimulated T cells and B cells expressed BSF-2 mRNA 48 h after stimulation. Immunohistochemical staining of the cells with anti-BSF-2 antibody demonstrated that macrophages, T cells and B cells could produce BSF-2. T cells in peripheral MNC produced BSF-2 in the presence of M phi. The requirement of macrophage for BSF-2 production in T cells could be replaced by TPA but not by IL-1 or BSF-2.
研究了外周血单个核细胞(MNC)中BSF-2/IL-6产生的调节。有丝分裂原刺激的MNC中BSF-2 mRNA表达呈双相反应,第一个峰值出现在约4小时,第二个峰值出现在约48小时。这是由MNC不同亚群中BSF-2 mRNA表达的不同动力学引起的;巨噬细胞(M phi)在无任何刺激的情况下于5小时表达BSF-2 mRNA,有丝分裂原刺激的T细胞和B细胞在刺激后48小时表达BSF-2 mRNA。用抗BSF-2抗体对细胞进行免疫组织化学染色表明,巨噬细胞、T细胞和B细胞均可产生BSF-2。外周MNC中的T细胞在有M phi存在时产生BSF-2。TPA可替代巨噬细胞对T细胞产生BSF-2的需求,但IL-1或BSF-2则不能。