Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh EH16 4SB, UK; Dementia Research Institute at Imperial College, Department of Brain Sciences, Imperial College London, London W12 0NN, UK.
Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh EH16 4SB, UK.
Semin Cell Dev Biol. 2023 Apr;139:13-23. doi: 10.1016/j.semcdb.2022.05.028. Epub 2022 Jun 9.
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 pathology in AD, from what we have learned from microscopy in terms of its impacts on synapse architecture, to the mechanistic role of Aβ, 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 molecular 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.
突触损失和损伤是阿尔茨海默病 (AD) 的核心特征,也是导致其行为和生理特征出现和发展的原因。在这里,我们回顾了描述 AD 中突触病理学的文献,从我们从显微镜学到的知识,包括其对突触结构的影响,到 Aβ、tau 和神经胶质细胞、线粒体功能障碍的作用机制,以及与 AD 风险基因的联系。我们考虑了一个新出现的观点,即突触病理学可能在进一步的水平上发挥作用,即突触多样性,并讨论了利用新的突触组图谱绘制方法来全面了解易损和有弹性突触的分子特性的前景。揭示 AD 对大脑突触多样性的影响应该为针对保留或补充丢失和损伤的突触的治疗方法提供信息,并有助于解释旨在测量突触损伤的临床成像方法。