Lepoivre M, Chenais B, Yapo A, Lemaire G, Thelander L, Tenu J P
Institut de Biochimie, Unité de Recherche Associée au Centre National de la Recherche Scientifique, Université de Paris-Sud, Orsay, France.
J Biol Chem. 1990 Aug 25;265(24):14143-9.
The murine adenocarcinoma cell line TA 3 synthesized nitrite from L-arginine upon stimulation with gamma-interferon (IFN-gamma) associated with tumor necrosis factor (TNF), and/or bacterial lipopolysaccharide (LPS), but not with IFN-gamma, TNF, or LPS added separately. Induction of the NO2(-)-generating activity caused an inhibition of DNA synthesis in TA 3 cells. This inhibition was prevented by the L-arginine analog N omega-nitro-L-arginine, which inhibited under the same conditions nitrite production by TA 3 cells. The TA 3 M2 subclone, selected for enhanced ribonucleotide reductase activity, was found to be less sensitive than the wild phenotype TA 3 WT to the cytostatic activity mediated by the NO2(-)-generating system. Cytosolic preparations from TA 3 M2 cells treated for 24 or 48 h with IFN-gamma, TNF, and LPS exhibited a reduced ribonucleotide reductase activity, compared to untreated control cells. No reduction in ribonucleotide reductase activity was observed when N omega-nitro-L-arginine was added to treated cells. Addition of L-arginine, NADPH, and tetrahydrobiopterin into cytosolic extracts from 24-h treated TA 3 M2 cells triggered the synthesis of metabolic products from the NO2(-)-generating pathway. This resulted in a dramatic inhibition of the residual ribonucleotide reductase activity present in the extracts. The inhibition was reversed by NG-monomethyl-L-arginine, another specific inhibitor of the NO2(-)-generating activity. No L-arginine-dependent inhibition of ribonucleotide reductase activity was observed using extracts from untreated cells that did not express NO2(-)-generating activity. These results demonstrate that, in an acellular preparation, molecules derived from the NO2(-)-generating pathway exert an inhibitory effect on the ribonucleotide reductase enzyme. This negative action might explain the inhibition of DNA synthesis induced in adenocarcinoma cells by the NO2(-)-generating pathway.
小鼠腺癌细胞系TA 3在受到与肿瘤坏死因子(TNF)相关的γ干扰素(IFN-γ)和/或细菌脂多糖(LPS)刺激时,能从L-精氨酸合成亚硝酸盐,但单独添加IFN-γ、TNF或LPS时则不能。亚硝酸盐生成活性的诱导导致TA 3细胞中DNA合成受到抑制。L-精氨酸类似物Nω-硝基-L-精氨酸可阻止这种抑制,该类似物在相同条件下也能抑制TA 3细胞产生亚硝酸盐。为增强核糖核苷酸还原酶活性而选择的TA 3 M2亚克隆,被发现对由亚硝酸盐生成系统介导的细胞生长抑制活性不如野生型TA 3 WT敏感。与未处理的对照细胞相比,用IFN-γ、TNF和LPS处理24或48小时的TA 3 M2细胞的胞质提取物显示核糖核苷酸还原酶活性降低。当向处理过的细胞中添加Nω-硝基-L-精氨酸时,未观察到核糖核苷酸还原酶活性降低。向经24小时处理的TA 3 M2细胞的胞质提取物中添加L-精氨酸、NADPH和四氢生物蝶呤,会引发亚硝酸盐生成途径代谢产物的合成。这导致提取物中存在的残余核糖核苷酸还原酶活性受到显著抑制。另一种亚硝酸盐生成活性的特异性抑制剂NG-单甲基-L-精氨酸可逆转这种抑制。使用未表达亚硝酸盐生成活性的未处理细胞的提取物,未观察到L-精氨酸依赖性的核糖核苷酸还原酶活性抑制。这些结果表明,在无细胞制剂中,亚硝酸盐生成途径衍生的分子对核糖核苷酸还原酶发挥抑制作用。这种负面作用可能解释了亚硝酸盐生成途径在腺癌细胞中诱导的DNA合成抑制。