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在帕金森病体内神经毒素模型中,CHOP/GADD153是黑质多巴胺能神经元凋亡性死亡的一个介质。

CHOP/GADD153 is a mediator of apoptotic death in substantia nigra dopamine neurons in an in vivo neurotoxin model of parkinsonism.

作者信息

Silva Robert M, Ries Vincent, Oo Tinmarla Frances, Yarygina Olga, Jackson-Lewis Vernice, Ryu Elizabeth J, Lu Phoebe D, Marciniak Stefan J, Ron David, Przedborski Serge, Kholodilov Nikolai, Greene Lloyd A, Burke Robert E

机构信息

Department of Neurology, The College of Physicians and Surgeons, Columbia University, New York 10032, USA.

出版信息

J Neurochem. 2005 Nov;95(4):974-86. doi: 10.1111/j.1471-4159.2005.03428.x. Epub 2005 Aug 31.

Abstract

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.

摘要

越来越多的证据表明,神经退行性疾病(如帕金森病)中的神经元死亡是由于程序性细胞死亡的激活。然而,细胞死亡的上游介质在很大程度上仍然未知。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。在由神经毒素诱导的组织培养模型中进行的此类分析已经确定了CHOP/GADD153的上调,CHOP/GADD153是一种转录因子,与内质网应激或氧化损伤引起的细胞凋亡有关。为了评估这些发现与疾病的相关性,我们研究了活体动物帕金森病神经毒素模型中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由1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的模型中观察到CHOP蛋白的核表达。在成年6OHDA模型中,CHOP是神经元死亡的介质,因为无效突变导致细胞凋亡减少。然而,在慢性MPTP模型中,虽然CHOP大量表达,但无效突变并不能防止神经元的丢失。我们得出结论,CHOP的作用取决于毒性刺激的性质。对于多巴胺的氧化代谢产物6OHDA,它是凋亡死亡的介质。

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