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首页> 外文期刊>Neurobiology of Aging: Experimental and Clinical Research >Increased pro-nerve growth factor and decreased brain-derived neurotrophic factor in non-Alzheimer's disease tauopathies
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Increased pro-nerve growth factor and decreased brain-derived neurotrophic factor in non-Alzheimer's disease tauopathies

机译:非阿尔茨海默氏病病因中神经生长因子的增加和脑源性神经营养因子的减少

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Alterations in the expression and signaling of brain-derived neurotrophic factor (BDNF) and the precursor to nerve growth factor (NGF), proNGF, play a role in the neuronal and cognitive dysfunction of Alzheimer's disease. Aggregated amyloid-β has been shown to down-regulate specific BDNF transcripts in Alzheimer's disease, but the role of tau pathology in neurotrophin dysregulation has not been investigated. We measured levels of BDNF mRNA and protein using real-time quantitative reverse transcription-polymerase chain reaction and enzyme-linked immunosorbent assay and proNGF protein using Western blotting in parietal cortex of subjects with tauopathies, neurodegenerative diseases exhibiting tau pathology without amyloid-β accumulation. We observed a significant increase in the level of proNGF protein in Pick's disease and a significant decrease in BDNF mRNA and protein levels in Pick's disease and corticobasal degeneration, but no neurotrophin alterations in progressive supranuclear palsy. The decrease in total BDNF mRNA levels in these tauopathies was predominantly due to down-regulation of transcript IV. These findings implicate tau pathology in neurotrophin dysregulation, which may represent a mechanism through which tau confers toxicity in Alzheimer's disease and related non-Alzheimer's dementias.
机译:脑源性神经营养因子(BDNF)和神经生长因子(NGF)的前体proNGF的表达和信号变化在阿尔茨海默氏病的神经元和认知功能障碍中起作用。已经显示,聚集的淀粉样蛋白β下调阿尔茨海默氏病中的特定BDNF转录物,但尚未研究tau病理在神经营养蛋白失调中的作用。我们使用实时定量逆转录-聚合酶链反应和酶联免疫吸附测定法测量BDNF mRNA和蛋白质的水平,并使用Western印迹法在患有taopathies,表现出tau病理但无淀粉样β堆积的神经变性疾病的受试者的顶叶皮质中测量proNGF蛋白。我们观察到匹克氏病中proNGF蛋白水平显着增加,匹克氏病和皮质基底变性中BDNF mRNA和蛋白水平显着降低,但在进行性核上性麻痹中无神经营养蛋白改变。在这些疾病中,总BDNF mRNA水平的降低主要是由于转录IV的下调。这些发现暗示tau病理学与神经营养蛋白失调有关,这可能代表tau赋予阿尔茨海默氏病和相关的非阿尔茨海默氏痴呆症毒性的机制。

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