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UV-A-induced decrease in nuclear factor-kappaB activity in human keratinocytes.

机译:UV-A诱导的人类角质形成细胞核因子-κB活性降低。

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摘要

Previous reports have demonstrated an increase in nuclear factor-kappaB (NF-kappaB) activity in response to UV radiation. These studies have essentially focused on the DNA-damaging fraction of solar UV radiation (UV-B and UV-C). In contrast, the effects of UV-A radiation (320-400 nm) on NF-kappaB are not well known. In this study, we present evidence that UV-A radiation induces a marked decrease in NF-kappaB DNA-binding activity in NCTC 2544 human keratinocytes. In addition, NCTC 2544 keratinocytes pretreated with UV-A fail to respond to NF-kappaB inducers. Moreover, UV-A radiation induces a decrease in NF-kappaB-driven luciferase reporter gene expression in NCTC 2544 keratinocytes. The expression of the gene encoding IkappaBalpha (IkappaB is the NF-kappaB inhibitor), which is closely associated with NF-kappaB activity, is also reduced (3-fold) upon UV-A treatment. Our results indicate that the UV-A-induced decrease in NF-kappaB DNA-binding activity is associated with a decrease in the levels of the p50 and p65 protein subunits. This is the first evidence that an oxidative stress, such as UV-A radiation, may induce a specific decrease in NF-kappaB activity in mammalian cells, probably through degradation of NF-kappaB protein subunits. These findings suggest that UV-A could modulate the NF-kappaB-dependent gene expression.
机译:以前的报告表明,响应紫外线辐射,核因子-κB(NF-kappaB)活性增加。这些研究基本上集中在太阳紫外线辐射的DNA破坏部分(UV-B和UV-C)上。相比之下,UV-A辐射(320-400 nm)对NF-κB的影响尚不清楚。在这项研究中,我们提供的证据表明,UV-A辐射在NCTC 2544人角质形成细胞中诱导NF-κBDNA结合活性显着降低。此外,用UV-A预处理的NCTC 2544角质形成细胞无法响应NF-κB诱导剂。此外,UV-A辐射诱导NCTC 2544角质形成细胞中NF-κB驱动的荧光素酶报道基因表达的减少。与NF-kappaB活性密切相关的编码IkappaBalpha(IkappaB是NF-kappaB抑制剂)的基因的表达在UV-A处理后也降低了(3倍)。我们的结果表明,UV-A诱导的NF-κBDNA结合活性降低与p50和p65蛋白亚基水平的降低有关。这是第一个证据,证明氧化应激(例如UV-A辐射)可能会导致NF-κB蛋白亚基降解,从而导致哺乳动物细胞中NF-κB活性特定降低。这些发现表明,UV-A可以调节NF-κB依赖性基因的表达。

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