Kleinerman E S, Fogler W E, Fidler I J
J Leukoc Biol. 1985 May;37(5):571-84. doi: 10.1002/jlb.37.5.571.
Cell-free culture supernatant fluids rich in macrophage-activating factor (MAF) activity were obtained from mitogen-stimulated human peripheral blood mononuclear leukocytes (MNL). The MAF preparations were incubated with human peripheral blood monocytes, rat alveolar macrophages (AM), and mouse peritoneal exudate macrophages (PEM). Only human monocytes were rendered tumorilytic against the human A375 melanoma cells, whereas rat AM or mouse PEM were not activated to lyse their respective syngeneic tumor targets. In contrast, once entrapped in multilamellar liposomes, the human MAF activated the human and rodent macrophages to become tumoricidal. The MAF activity was not due to contamination with endotoxins nor to the presence of gamma interferon. These data suggest that in contrast to macrophage surface receptors, which are species specific, the intracellular target sites for human MAF may cross species barriers.
富含巨噬细胞激活因子(MAF)活性的无细胞培养上清液,是从经丝裂原刺激的人外周血单核白细胞(MNL)中获得的。将MAF制剂与人外周血单核细胞、大鼠肺泡巨噬细胞(AM)和小鼠腹腔渗出液巨噬细胞(PEM)一起孵育。只有人单核细胞对人A375黑色素瘤细胞具有溶瘤作用,而大鼠AM或小鼠PEM未被激活以裂解其各自的同基因肿瘤靶标。相反,一旦包裹在多层脂质体中,人MAF就会激活人和啮齿动物的巨噬细胞,使其具有杀肿瘤作用。MAF活性不是由于内毒素污染,也不是由于γ干扰素的存在。这些数据表明,与物种特异性的巨噬细胞表面受体不同,人MAF的细胞内靶位点可能跨越物种屏障。