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首页> 外文期刊>Journal of Alzheimer's disease: JAD >Differential loss of synaptic proteins in Alzheimer's disease: Implications for synaptic dysfunction.
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Differential loss of synaptic proteins in Alzheimer's disease: Implications for synaptic dysfunction.

机译:阿尔茨海默氏病中突触蛋白的差异丢失:对突触功能障碍的影响。

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The objective of our research was to determine synaptic protein levels in brain specimens from AD subjects and age-matched control subjects. Further, to determine whether presynaptic or postsynaptic compartments of neurons are preferentially affected in AD patients, we studied 3 presynaptic vesicle proteins (synaptotagmin, synaptophysin, and Rab 3A), 2 synaptic membrane proteins (Gap 43 and synaptobrevin), and 2 postsynaptic proteins (neurogranin and synaptopodin) in specimens from AD and age-matched control brains. Two brain regions - the frontal and parietal cortices - were assessed for protein levels by immunoblotting analysis. We found a loss of both presynaptic vesicle proteins and postsynaptic proteins in all brain specimens from AD patients compared to those from age-matched control subjects. Further, we found that the loss of synaptic proteins was more severe in the frontal cortex brain specimens than in the parietal cortex brain specimens from the AD subjects compared to those from the controlsubjects, suggesting that the frontal brain may be critical for synaptic function in AD. Using immunohistochemistry techniques, we also determined the distribution pattern of all synaptic proteins in both the frontal and parietal cortices brain specimens from control subjects. Of the 7 synaptic proteins studied, the presynaptic proteins synaptophysin and rab 3A and the postsynaptic protein synaptopodin were the most down-regulated. Our study suggests that postsynaptic proteins and presynaptic proteins are important for synaptic function and may be related to cognitive impairments in AD.
机译:我们研究的目的是确定AD受试者和年龄匹配的对照受试者的脑标本中的突触蛋白水平。此外,为了确定在AD患者中神经元的突触前或突触后区室是否受到优先影响,我们研究了3种突触前囊泡蛋白(突触标记蛋白,突触素和Rab 3A),2种突触膜蛋白(Gap 43和synaptobrevin)和2种突触后蛋白( AD和年龄匹配的对照脑标本中的神经颗粒和突触足蛋白)。通过免疫印迹分析评估了两个大脑区域-额叶皮层和顶叶皮层-的蛋白质水平。我们发现与年龄匹配的对照受试者相比,AD患者的所有脑标本中突触前囊泡蛋白和突触后蛋白均丢失。此外,我们发现,与对照组相比,AD受试者的额叶皮层脑标本中突触蛋白的丢失要比顶叶皮质的脑标本中更严重,这表明额叶脑对于AD中的突触功能可能至关重要。 。使用免疫组织化学技术,我们还确定了来自对照组的额叶和顶叶皮质脑标本中所有突触蛋白的分布模式。在研究的7种突触蛋白中,突触前蛋白突触素和rab 3A和突触后蛋白突触足蛋白被下调最多。我们的研究表明,突触后蛋白和突触前蛋白对于突触功能很重要,并且可能与AD的认知障碍有关。

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