Palomer Ernest, Buechler Johanna, Salinas Patricia C
Department of Cell and Developmental Biology, University College London, London, United Kingdom.
Front Cell Neurosci. 2019 May 22;13:227. doi: 10.3389/fncel.2019.00227. eCollection 2019.
Growing evidence suggests that synaptic signaling is compromised in the aging brain and in Alzheimer's disease (AD), contributing to synaptic decline. Wnt signaling is a prominent pathway at the synapse and is required for synaptic plasticity and maintenance in the adult brain. In this review, we summarize the current knowledge on deregulation of Wnt signaling in the context of aging and AD. Emerging studies suggest that enhancing Wnt signaling could boost synaptic function during aging, and ameliorate synaptic pathology in AD. Although further research is needed to determine the precise contribution of deficient Wnt signaling to AD pathogenesis, targeting Wnt signaling components may provide novel therapeutic avenues for synapse protection or restoration in the brain.
越来越多的证据表明,衰老大脑和阿尔茨海默病(AD)中突触信号受损,导致突触衰退。Wnt信号是突触处的一条重要通路,对成人大脑的突触可塑性和维持至关重要。在本综述中,我们总结了衰老和AD背景下Wnt信号失调的现有知识。新出现的研究表明,增强Wnt信号可以在衰老过程中促进突触功能,并改善AD中的突触病理。尽管需要进一步研究以确定Wnt信号缺陷对AD发病机制的确切作用,但靶向Wnt信号成分可能为大脑中突触的保护或恢复提供新的治疗途径。