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正常中年及老年大脑和神经退行性疾病脑库的最低限度神经病理学诊断

Minimal neuropathologic diagnosis for brain banking in the normal middle-aged and aged brain and in neurodegenerative disorders.

作者信息

Alafuzoff Irina

机构信息

Department of Immunology, Genetics and Pathology, Uppsala University; Department of Clinical and Surgical Pathology, Uppsala University Hospital and Rudbeck Laboratory, Uppsala, Sweden.

出版信息

Handb Clin Neurol. 2018;150:131-141. doi: 10.1016/B978-0-444-63639-3.00010-4.

Abstract

Research on human brain diseases is currently often conducted on cell cultures and animals. Several questions however can only be addressed by studying human postmortem brain tissue. However, brain tissue obtained postmortem almost always displays pathology that is often related to the aging phenomenon. Thus, in order to be certain that the answers obtained are reliable, a systematic and thorough assessment of the brain tissue to be studied should be carried out. We are currently aware of several protein alterations that are found in middle-aged and aged brains that are obtained from neurologically unimpaired subjects. The most common alteration is hyperphosphorylation of τ, observed in both neurons and glial cells, in certain brain regions, followed by β-amyloid aggregation in the neuropil and vessel walls. Less common protein alterations are those noted for α-synuclein and Tar DNA-binding protein 43. It is noteworthy that these alterations, when found in excess, are diagnostic for various neurodegenerative diseases, such as Alzheimer disease, Pick disease, progressive supranuclear palsy, corticobasal degeneration, Parkinson disease, Lewy body dementia, and frontotemporal lobar degeneration. Since 1990, the neuropathology community has been aware that these protein alterations tend to progress in an orderly neuroanatomically defined manner and have thus designed a method to define a stage or a phase of the protein alteration. The neuropathology community has defined an initiation site, or neuroanatomic area that they presume the alteration originates from, and defined a presumed pattern of progression from the initiation site to other brain areas. Thus a reliable and reproducible description of each case regarding these alterations can be achieved. In addition to the above alterations, the brain tissue is also prone to various vascular alterations that should be registered as seen or not seen even if the significance of these alterations is still unclear.

摘要

目前,关于人类脑部疾病的研究通常在细胞培养物和动物身上进行。然而,有几个问题只能通过研究人类死后的脑组织来解决。然而,死后获得的脑组织几乎总是表现出与衰老现象相关的病理学特征。因此,为了确保所获得的答案可靠,应该对要研究的脑组织进行系统而全面的评估。我们目前已经了解到,在从中枢神经系统未受损的受试者身上获取的中年和老年大脑中发现了几种蛋白质改变。最常见的改变是τ蛋白的过度磷酸化,在某些脑区的神经元和神经胶质细胞中均有观察到,其次是神经纤维网和血管壁中的β-淀粉样蛋白聚集。较少见的蛋白质改变是α-突触核蛋白和Tar DNA结合蛋白43的改变。值得注意的是,当这些改变过量出现时,可诊断为各种神经退行性疾病,如阿尔茨海默病、皮克病、进行性核上性麻痹、皮质基底节变性、帕金森病、路易体痴呆和额颞叶痴呆。自1990年以来,神经病理学领域已经意识到这些蛋白质改变倾向于以一种有序的、由神经解剖学定义的方式进展,因此设计了一种方法来定义蛋白质改变的阶段或时期。神经病理学领域定义了一个起始部位,即他们推测改变起源的神经解剖学区域,并定义了从起始部位到其他脑区的假定进展模式。因此,可以对每个病例中这些改变进行可靠且可重复的描述。除了上述改变外,脑组织还容易出现各种血管改变,即使这些改变的意义尚不清楚,也应记录其是否存在。

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