Hauschildt S, Scheipers P, Bessler W G
Institute of Immunobiology, University of Freiburg, FRG.
Biochem Biophys Res Commun. 1991 Sep 16;179(2):865-71. doi: 10.1016/0006-291x(91)91898-m.
Stimulating bone marrow derived macrophages with LPS results in the induction of NO-synthase as measured by NO2- formation. Inhibitors of poly(ADP-ribose)polymerase, namely nicotinamide, 3-aminobenzamide and 3-methoxybenzamide, prevented NO2- formation in a dose dependent manner. Inhibition was most effective if the inhibitors were added at the same time as LPS. When added 10 h after exposure to LPS, a time at which expression of the enzyme had reached its maximum, no inhibition was observed. The inhibitors also blocked early events in activation such as protein and RNA-synthesis as well as DNA-synthesis. Thus prevention of NO2- formation may be related to inhibition of these events. Activation of macrophages by LPS was not accompanied by an increase but rather by a small decrease in ADP-ribosyltransferase activity. Whether this decrease plays a physiological role in activation needs further exploration.
用脂多糖刺激骨髓来源的巨噬细胞会导致通过亚硝酸盐形成来测量的一氧化氮合酶的诱导。聚(ADP - 核糖)聚合酶抑制剂,即烟酰胺、3 - 氨基苯甲酰胺和3 - 甲氧基苯甲酰胺,以剂量依赖的方式阻止了亚硝酸盐的形成。如果抑制剂与脂多糖同时添加,抑制效果最为显著。当在暴露于脂多糖10小时后添加时,此时酶的表达已达到最大值,则未观察到抑制作用。这些抑制剂还阻断了激活过程中的早期事件,如蛋白质和RNA合成以及DNA合成。因此,亚硝酸盐形成的预防可能与这些事件的抑制有关。脂多糖激活巨噬细胞并未伴随着ADP - 核糖基转移酶活性的增加,而是有小幅下降。这种下降在激活过程中是否发挥生理作用需要进一步探索。