Wechsler S J, Eurell T E, Russell S W
J Leukoc Biol. 1986 Aug;40(2):159-68. doi: 10.1002/jlb.40.2.159.
Regressing mouse Moloney sarcomas contain macrophages that are activated for tumor cell killing, while those found in progressively growing sarcomas either cannot kill or do so very poorly. Prostaglandin E2 (PGE2) has been shown to down-regulate macrophage activation in vitro. The study described here was designed, therefore, to ascertain and compare the concentrations of PGE2 in regressing and progressing Moloney sarcomas. Tumors were harvested for extraction and analyzed using conditions that minimized artifactual increases in PGE2 levels attributable to de novo synthesis. Concentrations of PGE2 were higher in progressing, compared to regressing, Moloney sarcomas during the early stages of tumor development. At nearly all time points, however, whether the neoplasms were of regressing or progressing type, the estimated concentrations of PGE2 in tumors exceeded the level that completely inhibits macrophage activation for tumor cell killing in vitro, that is, 10(-8) M. These data suggest either that PGE2 is not responsible for down-regulating activation in Moloney sarcomas or that, if PGE2 is responsible for the negative regulation of activation in progressing Moloney sarcomas, there must be something in regressing sarcomas that prevents the hormone from having its inhibitory effect.
消退期的小鼠莫洛尼肉瘤含有被激活以杀伤肿瘤细胞的巨噬细胞,而在进行性生长的肉瘤中发现的巨噬细胞要么不能杀伤肿瘤细胞,要么杀伤能力非常弱。前列腺素E2(PGE2)已被证明在体外可下调巨噬细胞的激活。因此,此处描述的研究旨在确定并比较消退期和进行性莫洛尼肉瘤中PGE2的浓度。采集肿瘤进行提取,并在尽量减少因重新合成导致PGE2水平人为升高的条件下进行分析。在肿瘤发展的早期阶段,与消退期莫洛尼肉瘤相比,进行性莫洛尼肉瘤中PGE2的浓度更高。然而,在几乎所有时间点,无论肿瘤是消退型还是进行型,肿瘤中PGE2的估计浓度都超过了在体外完全抑制巨噬细胞激活以杀伤肿瘤细胞的水平,即10^(-8) M。这些数据表明,要么PGE2与莫洛尼肉瘤中激活的下调无关,要么如果PGE2负责进行性莫洛尼肉瘤中激活的负调控,那么消退期肉瘤中必定存在某种物质阻止该激素发挥其抑制作用。