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黑磷纳米片通过降解聚集态的 α-突触核蛋白和清除帕金森病中的 ROS 来保护神经元。

Black Phosphorus Nanosheets Protect Neurons by Degrading Aggregative α-syn and Clearing ROS in Parkinson's Disease.

机构信息

Engineering Research Center for Molecular Medicine, College of Basic Medical Science, Guizhou Medical University, Guiyang, 561113, China.

Department of Biology, College of Basic Medical Science, Guizhou Medical University, Guiyang, 561113, China.

出版信息

Adv Mater. 2024 Jul;36(30):e2404576. doi: 10.1002/adma.202404576. Epub 2024 May 9.

DOI:10.1002/adma.202404576
PMID:38696266
Abstract

Although evidence indicates that the abnormal accumulation of α-synuclein (α-syn) in dopamine neurons of the substantia nigra is the main pathological feature of Parkinson's disease (PD), no compounds that have both α-syn antiaggregation and α-syn degradation functions have been successful in treating the disease in the clinic. Here, it is shown that black phosphorus nanosheets (BPNSs) interact directly with α-syn fibrils to trigger their disaggregation for PD treatment. Moreover, BPNSs have a specific affinity for α-syn through van der Waals forces. And BPNSs are found to activate autophagy to maintain α-syn homeostasis, improve mitochondrial dysfunction, reduce reactive oxygen species levels, and rescue neuronal death and synaptic loss in PC12 cells. It is also observed that BPNSs penetrate the blood-brain barrier and protect against dopamine neuron loss, alleviating behavioral disorders in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) induced mouse model and hA53T α-syn transgenic mice. Together, the study reveals that BPNSs have the potential as a novel integrated nanomedicine for clinical diagnosis and treatment of neurological diseases.

摘要

虽然有证据表明,多巴胺神经元中α-突触核蛋白(α-syn)的异常积累是帕金森病(PD)的主要病理特征,但在临床上,还没有既具有α-syn 抗聚集作用又具有 α-syn 降解功能的化合物成功用于治疗该疾病。在这里,研究表明黑磷纳米片(BPNSs)可以直接与α-syn 原纤维相互作用,从而触发其解聚,达到治疗 PD 的目的。此外,BPNSs 通过范德华力与 α-syn 具有特异性亲和力。并且发现 BPNSs 通过激活自噬来维持 α-syn 的体内平衡,改善线粒体功能障碍,降低活性氧水平,并挽救 PC12 细胞中的神经元死亡和突触损失。还观察到 BPNSs 可以穿透血脑屏障,防止多巴胺神经元的损失,从而缓解 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的小鼠模型和 hA53T α-syn 转基因小鼠的行为障碍。总的来说,该研究揭示了 BPNSs 具有作为一种新型综合神经疾病纳米药物用于临床诊断和治疗的潜力。

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