小胶质细胞
神经保护
血脑屏障
粒体自噬
氧化应激
神经科学
神经毒性
材料科学
纳米技术
医学
化学
生物
炎症
中枢神经系统
自噬
生物化学
免疫学
毒性
内科学
细胞凋亡
作者
Gang Zhong,Huiping Long,Tian Zhou,Yisi Liu,Jianping Zhao,Jinyu Han,Xiaohu Yang,Yu Yin,Fei Chen,Shengliang Shi
出处
期刊:Biomaterials
[Elsevier]
日期:2022-08-12
卷期号:288: 121690-121690
被引量:75
标识
DOI:10.1016/j.biomaterials.2022.121690
摘要
Current treatments for Alzheimer's disease (AD) that focus on inhibition of Aβ aggregation failed to show effectiveness in people who already had Alzheimer's symptoms. Strategies that synergistically exert neuroprotection and alleviation of oxidative stress could be a promising approach to correct the pathological brain microenvironment. Based on the key roles of microglia in modulation of AD microenvironment, we describe here the development of Prussian blue/polyamidoamine (PAMAM) dendrimer/Angiopep-2 (PPA) nanoparticles that can regulate the mitophagy of microglia as a potential AD treatment. PPA nanoparticles exhibit superior blood-brain barrier (BBB) permeability and exert synergistic effects of ROS scavenging and restoration of mitochondrial function of microglia. PPA nanoparticles effectively reduce neurotoxic Aβ aggregate and rescue the cognitive functions in APP/PS1 model mice. Together, our data suggest that these multifunctional dendrimer nanoparticles exhibit efficient neuroprotection and microglia modulation and can be exploited as a promising approach for the treatment of AD.
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