Okada M, Kishimoto T, Igarashi T, Teranishi T, Yamamura Y
J Immunol. 1978 Apr;120(4):1097-101.
The macrophage tumor cell line J774.1 replaced the function of normal macrophages in the induction of polyclonal killer T cells with 2-mercaptoethanol. J774.1 does not normally release soluble factor(s) which we have shown to be responsible for the differentiation of T cells to killer T cells. However, stimulation of J774.1 with LPS induced soluble factor(s) for T cell activation. An optimum concentration of LPS for the production of soluble factor(s) was 1 to 10 microgram/ml, which completely inhibited growth of the tumor cells. The production of soluble factor(s) was observed within 6 hr after LPS stimulation and reached its maximum level at 24 hr. Incubation of the cell line with 8Br-cyclic AMP and theophylline induced soluble factor(s), suggesting that LPS stimulation induced an increase in intracellular cyclic AMP which leads to the synthesis of soluble factor(s).
巨噬细胞肿瘤细胞系J774.1在用2-巯基乙醇诱导多克隆杀伤性T细胞时取代了正常巨噬细胞的功能。J774.1通常不释放可溶性因子,而我们已证明该因子负责T细胞向杀伤性T细胞的分化。然而,用脂多糖(LPS)刺激J774.1可诱导产生用于激活T细胞的可溶性因子。产生可溶性因子的LPS最佳浓度为1至10微克/毫升,这完全抑制了肿瘤细胞的生长。LPS刺激后6小时内可观察到可溶性因子的产生,并在24小时达到最高水平。用8-溴环磷酸腺苷(8Br-cyclic AMP)和茶碱孵育该细胞系可诱导产生可溶性因子,这表明LPS刺激导致细胞内环磷酸腺苷增加,从而导致可溶性因子的合成。