Rogalsky V, Svet-Moldavsky I, Arlin Z, Den T, Holland J F
Mount Sinai Medical Center, New York, NY 10029.
Biomed Pharmacother. 1988;42(8):547-53.
A new cytokine has been recognized in the conditioned media (CM) of freshly isolated acute myelocytic leukemia cells, cultured with 12-0-tetradecanayl phorbol acetate (TPA) 10(-8)M. The fraction with 70,000 MW was separated from CM by ammonium sulfate precipitation, ion-exchange cation and anion chromatography, and Sephadex G-200 gel filtration. It was a fibroblast growth inhibitor (FGI). This substance stopped fetal and skin (MALME 3 line) fibroblast propagation. The cytostatic effect was reversible on removal of FGI. At the same time, FGI did not inhibit macrophage proliferation. The fraction stimulated formation of monocytic and granulocytic colonies altered the phenotype of human U-2 osteosarcoma cells grown from epithelial-like to fibroblast-like cells, and stimulated differentiation of leukemic cells along the macrophage path. Some cells of promyelocytic leukemia line HL-60, grown in the presence of FGI, were stimulated to differentiate and some underwent lysis. The response to FGI of cells from different patients varied.
在与10(-8)M的12-氧-十四烷酰佛波醇-13-乙酸酯(TPA)一起培养的新鲜分离的急性髓细胞白血病细胞的条件培养基(CM)中,已识别出一种新的细胞因子。通过硫酸铵沉淀、离子交换阳离子和阴离子色谱以及Sephadex G-200凝胶过滤从CM中分离出分子量为70,000的部分。它是一种成纤维细胞生长抑制剂(FGI)。该物质可阻止胎儿和成纤维细胞(MALME 3系)的增殖。去除FGI后,细胞生长抑制作用是可逆的。同时,FGI不抑制巨噬细胞增殖。该部分刺激单核细胞和粒细胞集落的形成,改变了从上皮样生长为成纤维细胞样的人U-2骨肉瘤细胞的表型,并刺激白血病细胞沿巨噬细胞途径分化。在FGI存在下生长的早幼粒细胞白血病系HL-60的一些细胞被刺激分化,一些细胞发生裂解。来自不同患者的细胞对FGI的反应各不相同。