突触修剪
突触
神经科学
疾病
痴呆
补语(音乐)
认知
心理学
补体系统
小胶质细胞
生物
医学
免疫学
基因
免疫系统
表型
炎症
遗传学
病理
互补
作者
Lang Wen,Danlei Bi,Yong Shen
标识
DOI:10.1016/j.tins.2023.11.010
摘要
The complement system is increasingly recognized as a key player in the synapse loss and cognitive impairments observed in Alzheimer's disease (AD). In particular, the process of complement-dependent synaptic pruning through phagocytosis is over-activated in AD brains, driving detrimental excessive synapse elimination and contributing to synapse loss, which is the strongest neurobiological correlate of cognitive impairments in AD. Herein we review recent advances in characterizing complement-mediated synapse loss in AD, summarize the underlying mechanisms, and discuss the possible involvement of AD risk factors such as aging and various risk genes. We conclude with an overview of key questions that remain to be addressed.
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