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过氧化氢刺激血管平滑肌细胞中c-jun的转录:花生四烯酸的作用。

Hydrogen peroxide stimulates transcription of c-jun in vascular smooth muscle cells: role of arachidonic acid.

作者信息

Rao G N, Lassègue B, Griendling K K, Alexander R W

机构信息

Cardiology Division, Emory University School of Medicine, Atlanta, Georgia 30322.

出版信息

Oncogene. 1993 Oct;8(10):2759-64.

PMID:8378085
Abstract

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.

摘要

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。

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