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在氧化应激存在的情况下诱导帕金蛋白的表达。

Induction of parkin expression in the presence of oxidative stress.

作者信息

Yang Yan Xiang, Muqit Miratul M K, Latchman David S

机构信息

Medical Molecular Biology Unit, Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, UK.

出版信息

Eur J Neurosci. 2006 Sep;24(5):1366-72. doi: 10.1111/j.1460-9568.2006.04998.x.

Abstract

Parkinson's disease (PD) is one of the most common neurodegenerative disorders. Gene mutations have been found in rare familial forms of PD, with mutations in parkin being the most common cause. Oxidative stresses have also been implicated as an important contributing factor in the pathogenesis of PD. Currently, there is accumulating evidence that parkin may play a role in maintaining mitochondrial function and preventing oxidative stress. We demonstrated here that parkin is up-regulated when SH-SY5Y dopaminergic neuroblastoma cells are exposed to the oxidant dopamine. The up-regulation of parkin appeared to be due to transcriptional activation as luciferase assays confirmed that specific parkin promoter constructs could confer enhanced transcriptional activation in response to dopamine. Moreover, this effect was also seen when SH-SY5Y cells were subjected to another oxidative stress, 1-methyl-4-phenylpyridinium. In parallel with these studies, we also observed similar transcriptional activation of the parkin coregulated gene by oxidative stress. This is the first demonstration that parkin expression is up-regulated by oxidative stresses and may suggest that this might be a general neuroprotective response of parkin to oxidative stresses.

摘要

帕金森病(PD)是最常见的神经退行性疾病之一。在罕见的家族性帕金森病中发现了基因突变,其中parkin基因突变是最常见的原因。氧化应激也被认为是帕金森病发病机制中的一个重要促成因素。目前,越来越多的证据表明,parkin可能在维持线粒体功能和预防氧化应激方面发挥作用。我们在此证明,当SH-SY5Y多巴胺能神经母细胞瘤细胞暴露于氧化剂多巴胺时,parkin会被上调。parkin的上调似乎是由于转录激活,因为荧光素酶测定证实,特定的parkin启动子构建体可以在多巴胺的作用下增强转录激活。此外,当SH-SY5Y细胞受到另一种氧化应激物质1-甲基-4-苯基吡啶离子的作用时,也观察到了这种效应。与这些研究同时进行的是,我们还观察到氧化应激对parkin共调节基因有类似的转录激活作用。这是首次证明氧化应激可上调parkin的表达,这可能表明这是parkin对氧化应激的一种普遍的神经保护反应。

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