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研究阿尔茨海默病小鼠模型中小胶质细胞的超微结构改变以及与神经元应激、萎缩和退化的密切关系。

Investigating Microglial Ultrastructural Alterations and Intimate Relationships with Neuronal Stress, Dystrophy, and Degeneration in Mouse Models of Alzheimer's Disease.

机构信息

Axe neurosciences, Centre de recherche du CHU de Québec-Université Laval, Québec, QC, Canada.

Département de médecine moléculaire, Faculté de médecine, Université Laval, Québec, QC, Canada.

出版信息

Methods Mol Biol. 2022;2515:29-58. doi: 10.1007/978-1-0716-2409-8_3.

Abstract

In recent decades, microglia have taken the field of neuroscience by storm, with numerous studies identifying key roles for these cells in the pathophysiology of neurodegenerative conditions, such as Alzheimer's disease (AD). The heterogeneity of these cells (e.g., the presence of various subtypes like the disease-associated microglia, microglia associated with neurodegeneration, dark microglia, lipid droplet-accumulating microglia), and their ultrastructural alterations arising from environmental challenges have become a central focus of recent studies. Dark microglia are electron-dense cells defined by their ultrastructural markers of cellular stress using electron microscopy (EM). In this protocol, we first describe the steps required for proper brain tissue preparation for EM experiments. Ultrastructural analysis of microglia and neurons/synapses in AD mouse models is also detailed, using transmission or scanning EM. We next explain how to characterize several ultrastructural markers of cellular stress, dystrophy or degeneration, in microglia and neurons/synapses, with relation to amyloid beta plaques.

摘要

近几十年来,小胶质细胞在神经科学领域掀起了一场风暴,许多研究确定了这些细胞在神经退行性疾病(如阿尔茨海默病)的病理生理学中的关键作用。这些细胞的异质性(例如,存在各种亚型,如与疾病相关的小胶质细胞、与神经退行性变相关的小胶质细胞、暗小胶质细胞、脂质滴积累小胶质细胞)以及它们因环境挑战而产生的超微结构改变已成为最近研究的重点。暗小胶质细胞是电子致密细胞,使用电子显微镜(EM)通过其细胞应激的超微结构标志物来定义。在本方案中,我们首先描述了进行 EM 实验的脑组织准备所需的步骤。还详细介绍了使用透射或扫描 EM 对 AD 小鼠模型中小胶质细胞和神经元/突触的超微结构分析。接下来,我们解释了如何描述与淀粉样β斑块相关的小胶质细胞和神经元/突触中细胞应激、营养不良或退化的几种超微结构标志物。

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