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阿尔茨海默病中的白质改变:聚焦于髓鞘和少突胶质细胞。

White matter changes in Alzheimer's disease: a focus on myelin and oligodendrocytes.

机构信息

Department of Psychiatry, Columbia University, New York, NY, USA.

The Taub Institute for Research in Alzheimer's Disease and the Aging Brain, Columbia University, New York, NY, USA.

出版信息

Acta Neuropathol Commun. 2018 Mar 2;6(1):22. doi: 10.1186/s40478-018-0515-3.

Abstract

Alzheimer's disease (AD) is conceptualized as a progressive consequence of two hallmark pathological changes in grey matter: extracellular amyloid plaques and neurofibrillary tangles. However, over the past several years, neuroimaging studies have implicated micro- and macrostructural abnormalities in white matter in the risk and progression of AD, suggesting that in addition to the neuronal pathology characteristic of the disease, white matter degeneration and demyelination may be also important pathophysiological features. Here we review the evidence for white matter abnormalities in AD with a focus on myelin and oligodendrocytes, the only source of myelination in the central nervous system, and discuss the relationship between white matter changes and the hallmarks of Alzheimer's disease. We review several mechanisms such as ischemia, oxidative stress, excitotoxicity, iron overload, Aβ toxicity and tauopathy, which could affect oligodendrocytes. We conclude that white matter abnormalities, and in particular myelin and oligodendrocytes, could be mechanistically important in AD pathology and could be potential treatment targets.

摘要

阿尔茨海默病(AD)被认为是灰质中两种标志性病理变化的渐进后果:细胞外淀粉样斑块和神经原纤维缠结。然而,在过去的几年中,神经影像学研究表明,在 AD 的风险和进展中,白质的微观和宏观结构异常与微结构和脱髓鞘有关,这表明除了疾病特征性的神经元病理学外,白质退化和脱髓鞘也可能是重要的病理生理特征。在这里,我们重点关注髓鞘和少突胶质细胞,即中枢神经系统中唯一的髓鞘来源,综述 AD 中白质异常的证据,并讨论白质变化与阿尔茨海默病特征之间的关系。我们综述了几种机制,如缺血、氧化应激、兴奋性毒性、铁过载、Aβ毒性和tau 病,这些机制可能影响少突胶质细胞。我们的结论是,白质异常,特别是髓鞘和少突胶质细胞,在 AD 病理学中可能具有重要的机制作用,并且可能是潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bce/5834839/90c625d722cf/40478_2018_515_Fig1_HTML.jpg

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