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首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Neuroprotective effect of TNF alpha against the beta-amyloid neurotoxicity mediated by CDK5 kinase
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Neuroprotective effect of TNF alpha against the beta-amyloid neurotoxicity mediated by CDK5 kinase

机译:TNFα对CDK5激酶介导的β-淀粉样蛋白神经毒性的神经保护作用

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The tumor necrosis factor alpha (TNF alpha) plays a dual role in producing either neurodegeneration or neuroprotection in the central nervous system. Despite that TNFa was initially described as a cell death inductor, neuroprotective effects against cell death induced by several neurotoxic insults have been reported. Tau hyperphosphorylation and neuronal death found in Alzheimer disease is mediated by deregulation of the cdk5/p35 complex induced by A beta treatments. Since TNF alpha affects cdk5 activity, we investigated its possible protective role against the A beta-induced neurodegeneration, as mediated by cdk5. TNF alpha pretreatmen'ts significantly reduced the hippocampal neuronal cell death induced by the effects of A beta(42) peptide. In addition, this pretreatment reduced the increase in the activity of cdk5 induced by A beta(42) in primary neurons. Next, we investigated the Alzheimer type phosphorylation of tau protein induced by A beta(42). We observed that the pretreatment of neurons with TNF alpha reduces tau hyperphosphorylation. Taken together, these results define a novel neuroprotective effect of TNFa in preventing neuronal cell death and cdk5-dependent tau hyperphosphorylation. This phenomenon, taken together with other previous findings, suggests that the inflammatory response due to A beta peptide plays a key role in the development of Alzheimer etiopathogenesis. (c) 2006 Elsevier B.V. All rights reserved.
机译:肿瘤坏死因子α(TNF alpha)在中枢神经系统中神经变性或神经保护作用中起双重作用。尽管TNFα最初被描述为细胞死亡诱导剂,但已经报道了针对几种神经毒性损伤诱导的细胞死亡的神经保护作用。在Alzheimer病中发现的Tau过度磷酸化和神经元死亡是由A beta治疗诱导的cdk5 / p35复合物失控介导的。由于TNFα影响cdk5的活性,我们研究了它对cdk5介导的Aβ诱导的神经变性的可能的保护作用。 TNFα预处理可显着减少Aβ(42)肽的作用诱导的海马神经元细胞死亡。此外,这种预处理减少了由A beta(42)在原代神经元中诱导的cdk5活性的增加。接下来,我们研究了由A beta(42)诱导的tau蛋白的Alzheimer型磷酸化。我们观察到用TNFα预处理神经元可减少tau过度磷酸化。综上所述,这些结果定义了TNFα在预防神经元细胞死亡和cdk5依赖性tau过度磷酸化中的新型神经保护作用。这种现象与其他先前发现一起表明,由于Aβ肽引起的炎症反应在阿尔茨海默病的发病机理中起着关键作用。 (c)2006 Elsevier B.V.保留所有权利。

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