Hauschildt S, Scheipers P, Bessler W G, Mülsch A
Institute of Immunobiology, University of Freiburg, Federal Republic of Germany.
Biochem J. 1992 Nov 15;288 ( Pt 1)(Pt 1):255-60. doi: 10.1042/bj2880255.
The fibroblast cell line L929 contains a constitutively expressed NO synthase (EC 1.14.29.-) activity, which can be increased about 10-fold by tumour-necrosis factor alpha (TNF-alpha). Activities of the constitutive and the inducible enzymes are tetrahydrobiopterin-independent and can be inhibited by L-NG-nitroarginine. Induction of NO synthase by TNF-alpha was prevented by inhibitors of poly(ADP-ribose) polymerase, namely nicotinamide, 3-methoxybenzamide and 3-aminobenzamide. TNF-alpha did not lead to an increase in ADP-ribosyltransferase activity nor to a change in the pattern of ADP-ribosylated proteins. The inhibitors were only active during the first 4-5 h after exposure to TNF-alpha and they were found to suppress synthesis of protein, DNA and RNA. These data suggest that the inhibitors prevent induction of NO synthase by interference with RNA and protein synthesis. It is not yet known which reactions of these biosynthetic processes are affected by the inhibitors.
成纤维细胞系L929含有一种组成型表达的一氧化氮合酶(EC 1.14.29.-)活性,肿瘤坏死因子α(TNF-α)可使其活性增加约10倍。组成型酶和诱导型酶的活性不依赖四氢生物蝶呤,且可被L-NG-硝基精氨酸抑制。聚(ADP-核糖)聚合酶抑制剂,即烟酰胺、3-甲氧基苯甲酰胺和3-氨基苯甲酰胺,可阻止TNF-α对一氧化氮合酶的诱导。TNF-α不会导致ADP-核糖基转移酶活性增加,也不会使ADP-核糖基化蛋白的模式发生变化。这些抑制剂仅在暴露于TNF-α后的最初4-5小时内具有活性,并且发现它们会抑制蛋白质、DNA和RNA的合成。这些数据表明,抑制剂通过干扰RNA和蛋白质合成来阻止一氧化氮合酶的诱导。目前尚不清楚这些生物合成过程中的哪些反应会受到抑制剂的影响。