Takeda Y, Higuchi M, Sugimoto M, Shimoda O, Woo H J, Shimada S, Osawa T
Microbiol Immunol. 1986;30(2):143-54. doi: 10.1111/j.1348-0421.1986.tb00929.x.
Murine peritoneal macrophages elicited with a streptococcal preparation, OK-432, produced as much of a cytotoxic factor after stimulation with lipopolysaccharide (LPS) as BCG-elicited macrophages did. Proteose peptone-elicited macrophages produced a very small amount, if any, of the factor, and resident peritoneal macrophages did not release it at all even after LPS-stimulation. A newly established macrophage hybridoma, D/O-3.3, produced the factor after LPS-stimulation, but another hybridoma, D/O-3.2, did not. Experiments using these peritoneal macrophages and macrophage hybridomas demonstrated that macrophages can be divided into three subpopulations with regard to stages of activation for production of the cytotoxic factor. The first is fully activated macrophages which produce the factor after stimulation with LPS or MAF-C alone, the second is partially activated macrophages which produce the factor only after stimulation with a combination of recombinant interferon-gamma (rIFN-gamma) and LPS or rIFN-gamma and macrophage activating factor for cytotoxicity (MAF-C), and the third is nonactivated macrophages which cannot produce the factor at all.
用链球菌制剂OK-432诱导产生的小鼠腹腔巨噬细胞,在脂多糖(LPS)刺激后产生的细胞毒性因子与卡介苗诱导的巨噬细胞一样多。蛋白胨诱导的巨噬细胞即使产生该因子,量也非常少,而驻留腹腔巨噬细胞即使在LPS刺激后也根本不释放该因子。新建立的巨噬细胞杂交瘤D/O-3.3在LPS刺激后产生该因子,但另一种杂交瘤D/O-3.2则不产生。使用这些腹腔巨噬细胞和巨噬细胞杂交瘤进行的实验表明,就细胞毒性因子产生的激活阶段而言,巨噬细胞可分为三个亚群。第一个是完全激活的巨噬细胞,在用LPS或单独的巨噬细胞激活因子-细胞毒性(MAF-C)刺激后产生该因子;第二个是部分激活的巨噬细胞,仅在用重组干扰素-γ(rIFN-γ)与LPS或rIFN-γ与巨噬细胞激活因子-细胞毒性(MAF-C)联合刺激后才产生该因子;第三个是未激活的巨噬细胞,根本不能产生该因子。