神经保护
神经炎症
小胶质细胞
肽
帕金森病
多巴胺能
血脑屏障
载脂蛋白E
神经科学
活力测定
疾病
细胞
生物化学
多巴胺
炎症
免疫学
医学
生物
中枢神经系统
病理
作者
Juan Zhang,Bozhou Cui,Ting He,Ruoxuan Hei,Lan Yang,Chong Liu,Xianan Wu,Xi Wang,Zhaowei Gao,Fang Lin,Huizhong Zhang,Ke Dong
标识
DOI:10.1021/acsami.3c13849
摘要
Parkinson's disease (PD) affects millions of people's lives worldwide. The main pathogenesis of PD is dopaminergic neuron necrosis and neuroinflammation mediated by activated microglia cells. In recent years, the anti-inflammatory ability and neuroprotective effects of miR-124 in PD models were well proved, but the in vivo delivery of miR-124 remains challenging. Herein, we report a protein nanosystem modified with a brain-targeting peptide ApoE that could efficiently deliver miR-124 across the blood–brain barrier (BBB). This nanosystem showed good cell viability on brain endothelial cells and microglia cells, and administration of this nanosystem significantly decreased the neuroinflammation and dopaminergic neuron loss, as well as recovered parts of neurobehavioral deficits. This ApoE peptide-based protein nanosystem holds great promise for the delivery of RNA therapeutics to the brain and for realizing neuron protection in PD treatment.
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