Tomida M, Takenaga K, Yamamoto Y, Hozumi M
Biochem J. 1978 Dec 15;176(3):665-9. doi: 10.1042/bj1760665.
Mouse peritoneal macrophages release a factor(s) that stimulates differentiation of a mouse myeloid leukaemic cell line into mature granulocytes and macrophages. Treatment of the macrophages with the synthetic double-stranded polyribonucleotides poly(I).poly(C) and poly(A).poly(U) resulted in enhanced release of the factor into the culture medium. The effect was maximal after treatment with polyribonucleotides for 1 h, and the optimal dose of poly(I).poly(C) was 50 microgram/ml. The single-stranded polyribonucleotides poly(I) and poly(C) at the same concentration were far less effective. The differentiation-stimulating factor was detected not only in the cultured medium but also in the cell lysate. Exposure of macrophages to poly(I).poly(C) enhanced the total activity of the factor in both the culture medium and the cell lysate. The effect of this compound was blocked by the presence of cycloheximide. These results suggest that double-stranded polyribonucleotides enhance production of the differentiation-stimulating factor by peritoneal macrophages.
小鼠腹腔巨噬细胞释放一种因子,该因子可刺激小鼠髓样白血病细胞系分化为成熟的粒细胞和巨噬细胞。用合成的双链多聚核糖核苷酸聚(I)·聚(C)和聚(A)·聚(U)处理巨噬细胞,会导致该因子向培养基中的释放增加。用多聚核糖核苷酸处理1小时后效果最佳,聚(I)·聚(C)的最佳剂量为50微克/毫升。相同浓度的单链多聚核糖核苷酸聚(I)和聚(C)效果要差得多。不仅在培养基中,而且在细胞裂解物中都检测到了分化刺激因子。巨噬细胞暴露于聚(I)·聚(C)会增强培养基和细胞裂解物中该因子的总活性。环己酰亚胺的存在会阻断该化合物的作用。这些结果表明,双链多聚核糖核苷酸可增强腹腔巨噬细胞分化刺激因子的产生。