Introna M, Hamilton T A, Kaufman R E, Adams D O, Bast R C
J Immunol. 1986 Oct 15;137(8):2711-5.
Expression of the c-fos, c-myc, and c-fms proto-oncogenes has been studied in thioglycollate-elicited murine peritoneal macrophages after exposure to lipopolysaccharide (LPS). After incubation with LPS (20 ng/ml), a transient and rapid induction of the expression of c-fos and c-myc oncogenes could be observed, whereas the RNA levels for c-fms were not affected. Treatment with lipid A, the active moiety of the LPS molecule, increased the c-fos and c-myc expression to a comparable degree. Similar induction of c-fos and c-myc was observed after treatment with phorbol myristate acetate, suggesting that this effect of LPS on murine macrophages might be mediated through stimulation of protein kinase C. Under similar experimental conditions, LPS treatment of macrophages did not trigger DNA synthesis. Treatment with LPS blocked DNA synthesis in macrophages treated with L cell-conditioned medium containing colony-stimulating factor. Thus changes in c-fos and c-myc expression may be elements in the complex series of biochemical events that contribute to macrophage activation and are not necessarily related to induction or priming for cellular proliferation.
在暴露于脂多糖(LPS)后,已对巯基乙酸盐诱导的小鼠腹腔巨噬细胞中c-fos、c-myc和c-fms原癌基因的表达进行了研究。在用LPS(20 ng/ml)孵育后,可以观察到c-fos和c-myc原癌基因表达的短暂快速诱导,而c-fms的RNA水平未受影响。用LPS分子的活性部分脂多糖A处理,可使c-fos和c-myc表达增加到相当程度。在用佛波酯肉豆蔻酸酯乙酸盐处理后,观察到了类似的c-fos和c-myc诱导,这表明LPS对小鼠巨噬细胞的这种作用可能是通过刺激蛋白激酶C介导的。在类似的实验条件下,LPS处理巨噬细胞不会触发DNA合成。用含有集落刺激因子的L细胞条件培养基处理巨噬细胞时,LPS处理会阻断DNA合成。因此,c-fos和c-myc表达的变化可能是导致巨噬细胞活化的一系列复杂生化事件的组成部分,不一定与细胞增殖的诱导或启动有关。