Renier G, Lambert A
Department of Nutrition, Notre-Dame Hospital Research Center, Montreal, Quebec, Canada.
Arterioscler Thromb Vasc Biol. 1995 Mar;15(3):392-9. doi: 10.1161/01.atv.15.3.392.
Lipoprotein lipase (LPL) induces macrophage tumor necrosis factor-alpha (TNF-alpha) gene expression and protein secretion. Since TNF-alpha can increase interferon gamma (IFN-gamma)-dependent nitric oxide (NO) production, we studied whether LPL may synergize with IFN-gamma for the induction of macrophage NO production. Although ineffective by itself, LPL in combination with IFN-gamma increased L-arginine-dependent NO production in a dose-dependent manner. Preincubation of LPL with an anti-LPL neutralizing antibody totally suppressed this effect. Increased NO synthetase (NOS) mRNA expression was also observed after macrophage treatment with IFN-gamma and LPL. Protein synthesis was required for the induction of NOS mRNA, and a TNF-alpha-mediated effect of LPL on NOS gene expression and NO production was observed. The ability of LPL to augment IFN-gamma-dependent NOS mRNA expression was associated with an increase in the NOS gene transcriptional activity but not in the NOS mRNA stability. Finally, binding of nuclear proteins to the nuclear factor-kappa B- and TNF-alpha-responsive sequences of the macrophage NOS promotor was decreased by treatment of the cells by IFN-gamma alone or in combination with LPL. These data provide evidence for a link between LPL and arginine metabolism in macrophages and further stress the role of LPL in the regulation of macrophage activation.
脂蛋白脂肪酶(LPL)可诱导巨噬细胞肿瘤坏死因子-α(TNF-α)的基因表达和蛋白分泌。由于TNF-α可增加干扰素γ(IFN-γ)依赖性一氧化氮(NO)的产生,我们研究了LPL是否可与IFN-γ协同诱导巨噬细胞产生NO。LPL单独作用时无效,但与IFN-γ联合使用时,可剂量依赖性地增加L-精氨酸依赖性NO的产生。用抗LPL中和抗体预先孵育LPL可完全抑制这种效应。在用IFN-γ和LPL处理巨噬细胞后,还观察到一氧化氮合酶(NOS)mRNA表达增加。诱导NOS mRNA需要蛋白质合成,并且观察到LPL对NOS基因表达和NO产生具有TNF-α介导的效应。LPL增强IFN-γ依赖性NOS mRNA表达的能力与NOS基因转录活性的增加有关,而与NOS mRNA稳定性无关。最后,单独用IFN-γ或与LPL联合处理细胞可降低核蛋白与巨噬细胞NOS启动子的核因子-κB和TNF-α反应序列的结合。这些数据为LPL与巨噬细胞中精氨酸代谢之间的联系提供了证据,并进一步强调了LPL在调节巨噬细胞活化中的作用。