Department of Chemistry, University of Cambridge, Cambridge CB2 1EW, UK.
Department of Chemistry, University of Cambridge, Cambridge CB2 1EW, UK.; Department of Molecular Biosciences, Northwestern University, Evanston, IL 60208, USA.
Sci Adv. 2016 Aug 10;2(8):e1600947. doi: 10.1126/sciadv.1600947. eCollection 2016 Aug.
In Alzheimer's disease, aggregates of Aβ and tau in amyloid plaques and neurofibrillary tangles spread progressively across brain tissues following a characteristic pattern, implying a tissue-specific vulnerability to the disease. We report a transcriptional analysis of healthy brains and identify an expression signature that predicts-at ages well before the typical onset-the tissue-specific progression of the disease. We obtain this result by finding a quantitative correlation between the histopathological staging of the disease and the expression patterns of the proteins that coaggregate in amyloid plaques and neurofibrillary tangles, together with those of the protein homeostasis components that regulate Aβ and tau. Because this expression signature is evident in healthy brains, our analysis provides an explanatory link between a tissue-specific environmental risk of protein aggregation and a corresponding vulnerability to Alzheimer's disease.
在阿尔茨海默病中,淀粉样斑块和神经原纤维缠结中的 Aβ 和 tau 聚集物沿着特征性模式在脑组织中逐渐扩散,这表明疾病对组织具有特异性易感性。我们报告了一项对健康大脑的转录分析,并确定了一个表达特征,该特征可以在疾病典型发作之前的年龄很好地预测疾病的组织特异性进展。我们通过在疾病的组织病理学分期和共同聚集在淀粉样斑块和神经原纤维缠结中的蛋白质的表达模式之间找到定量相关性来获得此结果,同时还找到了调节 Aβ 和 tau 的蛋白质平衡成分。由于该表达特征在健康的大脑中明显存在,因此我们的分析为蛋白质聚集的组织特异性环境风险与对阿尔茨海默病的相应易感性之间提供了一个解释性联系。