Hong Soyon, Dissing-Olesen Lasse, Stevens Beth
Department of Neurology, F.M. Kirby Neurobiology Center, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Department of Neurology, F.M. Kirby Neurobiology Center, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Curr Opin Neurobiol. 2016 Feb;36:128-34. doi: 10.1016/j.conb.2015.12.004. Epub 2015 Dec 30.
Recent genome-wide association studies implicate microglia in Alzheimer's disease (AD) pathogenesis; however, their biological significance remains poorly understood. Synapse loss is a significant correlate of cognitive decline that serves as a critical hallmark of AD and other neurodegenerative diseases; however, mechanisms underlying synaptic vulnerability remain elusive. Emerging research on microglia function in the healthy brain is providing new insight into fundamental roles of microglia and immune molecules in brain wiring. Among their many roles, microglia prune developing synapses and regulate synaptic plasticity and function. Here, we review and discuss how this emerging work may provide new insight into how disruptions in microglia-synapse interactions could contribute to synapse loss and dysfunction, and consequently cognitive impairment, in AD.
最近的全基因组关联研究表明小胶质细胞与阿尔茨海默病(AD)的发病机制有关;然而,它们的生物学意义仍知之甚少。突触丧失是认知衰退的一个重要相关因素,是AD和其他神经退行性疾病的一个关键标志;然而,突触易损性的潜在机制仍然难以捉摸。关于健康大脑中小胶质细胞功能的新研究正在为小胶质细胞和免疫分子在大脑布线中的基本作用提供新的见解。在它们众多的作用中,小胶质细胞修剪发育中的突触并调节突触可塑性和功能。在这里,我们回顾并讨论这项新研究如何为小胶质细胞-突触相互作用的破坏如何导致AD中的突触丧失和功能障碍,进而导致认知障碍提供新的见解。