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Proteomic analysis of neurons microdissected from formalin-fixed paraffin-embedded Alzheimer’s disease brain tissue

机译:从福尔马林固定石蜡包埋的阿尔茨海默氏病脑组织显微解剖的神经元的蛋白质组学分析

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摘要

The vast majority of human tissue specimens are formalin-fixed, paraffin embedded (FFPE) archival samples, making this type of tissue a potential gold mine for medical research. It is now accepted that proteomics can be done using FFPE tissue and can generate similar results as snap-frozen tissue. However, the current methodology requires a large amount of starting protein, limiting the questions that can be answered in these types of proteomics studies and making cell-type specific proteomics studies difficult. Cell-type specific proteomics has the potential to greatly enhance understanding of cell functioning in both normal and disease states. Therefore, here we describe a new method that allows localized proteomics on individual cell populations isolated from FFPE tissue sections using laser capture microdissection. To demonstrate this technique we microdissected neurons from archived tissue blocks of the temporal cortex from patients with Alzheimer’s disease. Using this method we identified over 400 proteins in microdissected neurons; on average 78% that were neuronal and 50% that were associated with Alzheimer’s disease. Therefore, this technique is able to provide accurate and meaningful data and has great potential for any future study that wishes to perform localized proteomics using very small amounts of archived FFPE tissue.
机译:绝大多数人体组织标本是福尔马林固定,石蜡包埋(FFPE)的档案样品,使此类组织成为医学研究的潜在金矿。现在已经公认,蛋白质组学可以使用FFPE组织完成,并且可以产生与速冻组织相似的结果。但是,当前的方法学需要大量的起始蛋白质,限制了在这些类型的蛋白质组学研究中可以回答的问题,并使细胞类型特异性蛋白质组学研究变得困难。细胞类型特异性蛋白质组学有潜力极大地增进人们对正常和疾病状态下细胞功能的了解。因此,在这里,我们描述了一种新方法,该方法允许使用激光捕获显微切割技术从FFPE组织切片中分离出的单个细胞群体上进行蛋白质组学定位。为了证明该技术,我们从阿尔茨海默氏病患者的颞皮质存档组织块中显微解剖了神经元。使用这种方法,我们在显微解剖的神经元中发现了400多种蛋白质。平均有78%的神经元和50%与阿尔茨海默氏病有关。因此,该技术能够提供准确和有意义的数据,并且对于希望使用很少量的FFPE组织进行局部蛋白质组学的任何未来研究都具有巨大的潜力。

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