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Characterization of the novel protein P9TLDR (temporal lobe down-regulated) with a brain-site-specific gene expression modality in Alzheimer's disease brain

机译:在阿尔茨海默氏病脑中具有特定于大脑位点的基因表达方式的新型蛋白P9TLDR(下垂颞叶)的表征

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摘要

Alzheimer's disease (AD) is an aging-related neurodegenerative disorder characterized by irreversible loss of higher cognitive functions. The disease is characterized by the presence of amyloid plaques and neurofibrillary tangles (NFT). In the current study we isolated from an intra-cerebral brain-site-specific (AD temporal lobe vs. AD occipital lobe) polymerase chain reaction (PCR)-select cDNA suppression subtractive hybridization (PCR-cDNA-SSH) expression analysis the novel gene P9TLDR, potentially a microtubule-associated protein involved in neuronal migration, with an altered expression pattern: down-regulated in the temporal lobe cortex of early stage AD brains. In an in vitro AD-related cell model, amyloid-β peptide (Aβ)-treated neurons, reduced P9TLDR expression correlated with increased tau protein phosphorylation. In conclusion, interference with the P9TLDR signalling pathways might be a therapeutic strategy for the treatment of AD.
机译:阿尔茨海默氏病(AD)是一种与衰老相关的神经退行性疾病,其特征是不可逆的高级认知功能丧失。该疾病的特征在于存在淀粉样斑块和神经原纤维缠结(NFT)。在本研究中,我们从脑内特定部位(AD颞叶vs. AD枕叶)聚合酶链反应(PCR)-选择cDNA抑制消减杂交(PCR-cDNA-SSH)表达分析中分离出了新基因P9TLDR,可能是与神经元迁移有关的微管相关蛋白,其表达模式发生了变化:在早期AD大脑的颞叶皮层中被下调。在体外AD相关的细胞模型中,淀粉样蛋白-β肽(Aβ)处理的神经元减少的P9TLDR表达与增加的tau蛋白磷酸化相关。总之,干扰P9TLDR信号通路可能是AD治疗的一种治疗策略。

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