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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >CHOP/GADD153 is a mediator of apoptotic death in substantia nigra dopamine neurons in an in vivo neurotoxin model of parkinsonism.
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CHOP/GADD153 is a mediator of apoptotic death in substantia nigra dopamine neurons in an in vivo neurotoxin model of parkinsonism.

机译:CHOP / GADD153是帕金森氏症体内神经毒素模型中黑质多巴胺神经元凋亡死亡的介体。

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There is increasing evidence that neuron death in neurodegenerative diseases, such as Parkinson's disease, is due to the activation of programmed cell death. However, the upstream mediators of cell death remain largely unknown. One approach to the identification of upstream mediators is to perform gene expression analysis in disease models. Such analyses, performed in tissue culture models induced by neurotoxins, have identified up-regulation of CHOP/GADD153, a transcription factor implicated in apoptosis due to endoplasmic reticulum stress or oxidative injury. To evaluate the disease-related significance of these findings, we have examined the expression of CHOP/GADD153 in neurotoxin models of parkinsonism in living animals. Nuclear expression of CHOP protein is observed in developmental and adult models of dopamine neuron death induced by intrastriatal injection of 6-hydroxydopamine (6OHDA) and in models induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). CHOP is a mediator of neuron death in the adult 60HDA model because a null mutation results in a reduction in apoptosis. In the chronic MPTP model, however, while CHOP is robustly expressed, the null mutation does not protect from the loss of neurons. We conclude that the role of CHOP depends on the nature of the toxic stimulus. For 6OHDA, an oxidative metabolite of dopamine, it is a mediator of apoptotic death.
机译:越来越多的证据表明,神经退行性疾病(例如帕金森氏病)中的神经元死亡是由于程序性细胞死亡的激活所致。但是,细胞死亡的上游介体仍然未知。鉴定上游介质的一种方法是在疾病模型中进行基因表达分析。在神经毒素诱导的组织培养模型中进行的此类分析已鉴定出CHOP / GADD153的上调,CHOP / GADD153是一种由于内质网应激或氧化损伤而导致细胞凋亡的转录因子。为了评估这些发现与疾病相关的重要性,我们检查了在活动性动物帕金森氏症神经毒素模型中CHOP / GADD153的表达。在纹状体内注射6-羟基多巴胺(6OHDA)诱导的多巴胺神经元死亡的发育和成年模型以及1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导的模型中观察到CHOP蛋白的核表达MPTP)。 CHOP是成人60HDA模型中神经元死亡的介体,因为无效突变会导致凋亡减少。然而,在慢性MPTP模型中,虽然CHOP得到了强有力的表达,但无效突变并不能保护神经元免受损失。我们得出结论,CHOP的作用取决于毒性刺激的性质。对于6OHDA(一种多巴胺的氧化代谢产物),它是细胞凋亡死亡的媒介。

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