小胶质细胞
神经毒性
自噬
吞噬作用
分泌物
淀粉样蛋白(真菌学)
细胞外
细胞生物学
神经炎症
淀粉样前体蛋白
肽
化学
炎症
神经科学
阿尔茨海默病
医学
生物
疾病
免疫学
生物化学
毒性
病理
细胞凋亡
无机化学
有机化学
作者
Yu Zhao,Qiushi Li,Qingqing Huang,Yang Liu
标识
DOI:10.1002/marc.202300378
摘要
Cerebral soluble β-amyloid aggregates (sAβs) accumulation is one of the most important causes in Alzheimer's disease (AD) progression. In order to mitigate the neurotoxicity induced by sAβs and achieve enhanced AD therapeutic outcomes, robust sAβs clearance become an emerging task. Herein, a self-destructive nanoscavenger (SDNS) is reported based on multifunctional peptide-polymer complexes that can capture extracellular sAβs via hydrogen-bonding interactions and deliver them into microglial lysosomes. The internalized SDNS then occurs self-destruction within lysosomes and upregulates autophagy, thereby promoting the degradation of neurotoxic sAβs. Importantly, the enhanced autophagy also significantly suppresses the secretion of inflammatory factors by microglia, which is induced by internalized sAβs. Given that cerebral persistent inflammatory environment disturbs microglia-mediated phagocytosis and degradation, it is believed that this synergistic approach has valuable potential as a therapeutic strategy for AD.
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