Zacharchuk C M, Drysdale B E, Mayer M M, Shin H S
Proc Natl Acad Sci U S A. 1983 Oct;80(20):6341-5. doi: 10.1073/pnas.80.20.6341.
Guinea pig peritoneal macrophages, when activated for cytotoxicity by the calcium ionophore A23187 or lipopolysaccharide, produce a cytotoxic factor [macrophage cytotoxic factor (M phi-CF)] that is not blocked by catalase or protease inhibitors. Fractionation of culture supernates containing M phi-CF by gel filtration revealed one peak of cytotoxic activity of Mr approximately 45,000, the same as guinea pig lymphotoxin (LT). Antiserum prepared against purified guinea pig LT completely neutralized the cytotoxic activity of M phi-CF. In addition, the cytotoxic factor in guinea pig tumor necrosis serum was found to have a Mr of 45,000 and was neutralized by anti-LT. Thus, M phi-CF is physicochemically and immunochemically similar to LT and tumor necrosis factor, if not identical. To investigate the role of M phi-CF in macrophage-mediated cytotoxicity, anti-LT was added to A23187- or lipopolysaccharide-activated macrophages before addition of L-929 target cells. In 10 of 16 experiments, the inhibition of macrophage-mediated cytotoxicity was 100%. In the others, cytotoxicity was blocked partially, the lowest inhibition being 49%. The effectiveness of inhibition appeared to be inversely related to the intensity of macrophage activation. These results indicate that M phi-CF plays a significant role in macrophage-mediated cytotoxicity but involvement of another mechanism cannot be excluded.
豚鼠腹腔巨噬细胞经钙离子载体A23187或脂多糖激活产生细胞毒性时,会产生一种细胞毒性因子[巨噬细胞细胞毒性因子(M phi-CF)],该因子不受过氧化氢酶或蛋白酶抑制剂的阻断。通过凝胶过滤对含有M phi-CF的培养上清液进行分级分离,发现有一个细胞毒性活性峰,其Mr约为45,000,与豚鼠淋巴毒素(LT)相同。针对纯化的豚鼠LT制备的抗血清完全中和了M phi-CF的细胞毒性活性。此外,发现豚鼠肿瘤坏死血清中的细胞毒性因子Mr为45,000,并被抗LT中和。因此,M phi-CF在物理化学和免疫化学上与LT和肿瘤坏死因子相似,即便不完全相同。为了研究M phi-CF在巨噬细胞介导的细胞毒性中的作用,在加入L-929靶细胞之前,将抗LT添加到经A23187或脂多糖激活的巨噬细胞中。在16个实验中的10个实验中,巨噬细胞介导的细胞毒性抑制率为100%。在其他实验中,细胞毒性被部分阻断,最低抑制率为49%。抑制效果似乎与巨噬细胞激活的强度呈负相关。这些结果表明,M phi-CF在巨噬细胞介导的细胞毒性中起重要作用,但不能排除另一种机制的参与。