Rao G N, Lassègue B, Griendling K K, Alexander R W
Cardiology Division, Emory University School of Medicine, Atlanta, Georgia 30322.
Oncogene. 1993 Oct;8(10):2759-64.
We reported previously that hydrogen peroxide induces DNA synthesis in rat aortic smooth muscle (RASM) cells. In the present paper we studied the mechanism by which hydrogen peroxide induces c-jun mRNA, an early response gene whose activation is required for mitogen-stimulated cell growth. Hydrogen peroxide induced c-jun mRNA in growth-arrested RASM cells in a time dependent manner. This stimulation was significantly inhibited by mepacrine, a phospholipase A2 (PLA2) inhibitor. Arachidonic acid, a PLA2 product, also increased c-jun mRNA with a time course similar to that of hydrogen peroxide. The increases in c-jun mRNA induced by hydrogen peroxide and arachidonic acid were significantly reduced (55%) by down-regulation of protein kinase C with a phorbol ester. Furthermore, the effect of hydrogen peroxide on c-jun mRNA was also reduced by NDGA, an inhibitor of the lipoxygenase-cytochrome P450 mono-oxygenase system, suggesting that metabolism of arachidonic acid through this pathway is required for the induction of c-jun mRNA by oxidants. Both hydrogen peroxide and arachidonic acid significantly increased c-jun transcription as demonstrated by nuclear run-on assays. Together these observations suggest that: (1) the induction of c-jun mRNA by hydrogen peroxide is mediated by PLA2-dependent arachidonic acid release and metabolism through the lipoxygenase-cytochrome P450 mono-oxygenase system; (2) PKC appears to be involved in this signaling pathway and (3) the induction of c-jun mRNA by hydrogen peroxide in RASM cells is due to increased transcription.
我们之前报道过,过氧化氢可诱导大鼠主动脉平滑肌(RASM)细胞中的DNA合成。在本文中,我们研究了过氧化氢诱导c-jun mRNA的机制,c-jun mRNA是一种早期反应基因,其激活是有丝分裂原刺激细胞生长所必需的。过氧化氢以时间依赖性方式诱导生长停滞的RASM细胞中的c-jun mRNA。这种刺激被磷脂酶A2(PLA2)抑制剂米帕林显著抑制。PLA2的产物花生四烯酸也增加了c-jun mRNA,其时间进程与过氧化氢相似。用佛波酯下调蛋白激酶C后,过氧化氢和花生四烯酸诱导的c-jun mRNA增加显著降低(55%)。此外,脂氧合酶-细胞色素P450单加氧酶系统的抑制剂NDGA也降低了过氧化氢对c-jun mRNA的作用,这表明通过该途径的花生四烯酸代谢是氧化剂诱导c-jun mRNA所必需的。核转录分析表明,过氧化氢和花生四烯酸均显著增加了c-jun转录。这些观察结果共同表明:(1)过氧化氢诱导c-jun mRNA是由PLA2依赖性花生四烯酸释放并通过脂氧合酶-细胞色素P450单加氧酶系统代谢介导的;(2)蛋白激酶C似乎参与了该信号通路;(3)过氧化氢在RASM细胞中诱导c-jun mRNA是由于转录增加。