Sone S, Poste G, Fidler I J
J Immunol. 1980 May;124(5):2197-202.
Alveolar macrophages (AM) obtained from F344 rats were rendered tumoricidal by incubation in vitro with cellfree culture supernatant fluids rich in macrophage-activating factor (MAF) activity harvested from mitogen-stimulated F344 rat lymphocytes. AM activated by this procedure destroyed syngeneic, allogeneic, and xenogeneic tumor cells but were not cytotoxic for nonneoplastic cells. MAF was encapsulated in multilamellar lipid vesicles (liposomes) and its ability to render AM tumoricidal was compared with that of free (unencapsulated) MAF. Liposome-encapsulated MAF rendered AM cytotoxic at concentrations up to 16,000 times lower than free MAF. These data demonstrate that AM can respond in vitro to lymphokines and that MAF encapsulated within liposomes is far more efficient in rendering AM tumoridical than free MAF.
从F344大鼠获得的肺泡巨噬细胞(AM),通过与富含巨噬细胞激活因子(MAF)活性的无细胞培养上清液在体外孵育而具有杀肿瘤活性,该上清液取自丝裂原刺激的F344大鼠淋巴细胞。通过此程序激活的AM可破坏同基因、异基因和异种肿瘤细胞,但对非肿瘤细胞无细胞毒性。MAF被包裹在多层脂质囊泡(脂质体)中,并将其使AM具有杀肿瘤活性的能力与游离(未包裹)MAF的能力进行比较。脂质体包裹的MAF在浓度比游离MAF低至16000倍时仍能使AM具有细胞毒性。这些数据表明,AM在体外可对淋巴因子作出反应,并且包裹在脂质体内的MAF在使AM具有杀肿瘤活性方面比游离MAF效率高得多。