Luettig B, Decker T, Lohmann-Matthes M L
Fraunhofer Institute for Toxicology, Hannover, FRG.
J Immunol. 1989 Dec 15;143(12):4034-8.
Plasma membranes were isolated from thioglycolate-induced peritoneal mouse macrophages and tested directly in a 51Cr-release assay against WEHI 164 tumor cells. These membranes showed anti-TNF antibody inhibitable killing of the TNF-sensitive tumor cell line, indicating that membrane-associated TNF is present on mouse macrophages. In order to elucidate whether membrane TNF is an integral protein or a molecule attached to a receptor, cells and plasma membranes were treated with low pH buffer. A partial reduction in TNF activity was observed which could be restored by incubation with exogenous TNF. In a Western blot analysis the integral membrane TNF could be identified as the 26-kDa molecule on activated mouse macrophages. These results indicate that both forms of membrane-associated TNF exist on macrophages and are responsible for cell-mediated cytotoxicity against TNF-alpha-sensitive targets.
从巯基乙酸盐诱导的小鼠腹腔巨噬细胞中分离出质膜,并直接在51Cr释放试验中针对WEHI 164肿瘤细胞进行测试。这些质膜显示出对TNF敏感的肿瘤细胞系具有抗TNF抗体可抑制的杀伤作用,表明膜相关TNF存在于小鼠巨噬细胞上。为了阐明膜TNF是一种整合蛋白还是附着在受体上的分子,细胞和质膜用低pH缓冲液处理。观察到TNF活性部分降低,通过与外源性TNF孵育可恢复。在蛋白质印迹分析中,完整的膜TNF可被鉴定为活化小鼠巨噬细胞上的26 kDa分子。这些结果表明,巨噬细胞上存在两种形式的膜相关TNF,它们负责对TNF-α敏感靶标的细胞介导细胞毒性。