Synapse pathology in Alzheimer?s disease

被引:48
|
作者
Griffiths, Jessica [1 ,2 ]
Grant, Seth G. N. [1 ]
机构
[1] Univ Edinburgh, Ctr Clin Brain Sci, Edinburgh EH16 4SB, Scotland
[2] Imperial Coll London, Imperial Coll, Dept Brain Sci, Dementia Res Inst, London W12 0NN, England
基金
英国医学研究理事会;
关键词
Synapse; Synaptome; Alzheimer?s disease; Microscopy; A; Tau; HIPPOCAMPAL DENTATE GYRUS; OLIGOMERIC AMYLOID-BETA; A-BETA; QUANTITATIVE ASSESSMENT; PROTEOMIC ANALYSIS; DENDRITIC SPINES; MITOCHONDRIAL DYSFUNCTION; HYPERPHOSPHORYLATED TAU; PROTEIN SYNAPTOPHYSIN; POSTSYNAPTIC DENSITY;
D O I
10.1016/j.semcdb.2022.05.028
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Synapse loss and damage are central features of Alzheimer's disease (AD) and contribute to the onset and progression of its behavioural and physiological features. Here we review the literature describing synapse pa-thology in AD, from what we have learned from microscopy in terms of its impacts on synapse architecture, to the mechanistic role of A beta, tau and glial cells, mitochondrial dysfunction, and the link with AD risk genes. We consider the emerging view that synapse pathology may operate at a further level, that of synapse diversity, and discuss the prospects for leveraging new synaptome mapping methods to comprehensively understand the mo-lecular properties of vulnerable and resilient synapses. Uncovering AD impacts on brain synapse diversity should inform therapeutic approaches targeted at preserving or replenishing lost and damaged synapses and aid the interpretation of clinical imaging approaches that aim to measure synapse damage.
引用
收藏
页码:13 / 23
页数:11
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