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首页> 外文期刊>Journal of biochemical and molecular toxicology >Activation of metallothionein transcription by 4-hydroxynonenal.
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Activation of metallothionein transcription by 4-hydroxynonenal.

机译:通过4-羟基壬烯醛激活金属硫蛋白转录。

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摘要

Metallothioneins (MTs) protect cells from oxidative damage by scavenging reactive oxygen species (ROS). Concurrent with protecting cells from ROS-mediated damage, MT transcription is induced by ROS. ROS activate transcription by affecting several signal transduction pathways, many of which have been implicated in regulating MT transcription. ROS-activated intracellular signaling is mediated by the stable lipid peroxide 4-hydroxynonenal (HNE). After determining the level of sensitivity of Hepa 1-6 cells to HNE, MT-1 mRNA expression was shown to be induced in a concentration and time-dependent manner after HNE exposure. Finally, using MT-based reporters, HNE was found to induce MT transcription via both antioxidant response and metal response elements. Thus, ROS may activate MT transcription by generating HNE that in turn affects signaling pathways that regulate MT transcription via the transcription factors AP-1 and MTF-1.
机译:金属硫蛋白(MTs)通过清除活性氧(ROS)保护细胞免受氧化损伤。在保护细胞免受ROS介导的损伤的同时,ROS诱导MT转录。 ROS通过影响几种信号转导途径来激活转录,其中许多信号转导途径与调节MT转录有关。 ROS激活的细胞内信号传导由稳定的脂质过氧化物4-羟基壬烯醛(HNE)介导。在确定Hepa 1-6细胞对HNE的敏感性水平后,显示HNE暴露后MT-1 mRNA表达以浓度和时间依赖性方式被诱导。最后,使用基于MT的报道分子,发现HNE通过抗氧化剂响应和金属响应元素诱导MT转录。因此,ROS可以通过产生HNE来激活MT转录,而HNE又会影响通过转录因子AP-1和MTF-1调节MT转录的信号通路。

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