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神经递质衍生脂质体-蛋白水解靶向嵌合体-脱氧核糖核酸纳米复合物的全身给药促进tau蛋白清除及认知恢复用于阿尔茨海默病治疗

Systemic Administration of Neurotransmitter-Derived Lipidoids-PROTACs-DNA Nanocomplex Promotes Tau Clearance and Cognitive Recovery for Alzheimer's Disease Therapy.

作者信息

Gong Baofeng, Zhang Weicong, Cong Wei, Gu Yuankai, Ji Wenbo, Yin Tong, Zhou Honglei, Hu Honggang, Zhuang Jianhua, Luo Yi, Liu Yan, Gao Jie, Yin You

机构信息

Department of Neurology, Second Affiliated Hospital (Shanghai Changzheng Hospital) of Naval Medical University, Shanghai, 200003, China.

School of Pharmacy, University College London, London, WC1N 1AX, UK.

出版信息

Adv Healthc Mater. 2024 Dec;13(32):e2400149. doi: 10.1002/adhm.202400149. Epub 2024 Jul 15.

Abstract

Alzheimer's disease (AD) poses a significant burden on the economy and healthcare systems worldwide. Although the pathophysiology of AD remains debatable, its progression is strongly correlated with the accumulation of tau aggregates. Therefore, tau clearance from brain lesions can be a promising strategy for AD therapy. To achieve this, the present study combined proteolysis-targeting chimera (PROTAC), a novel protein-degradation technique that mediates degradation of target proteins via the ubiquitin-proteasome system, and a neurotransmitter-derived lipidoid (NT-lipidoid) nanoparticle delivery system with high blood-brain barrier-penetration activity, to generate a novel nanomedicine named NPD. Peptide 1, a cationic tau-targeting PROTAC is loaded onto the positively charged nanoparticles using DNA-intercalation technology. The resulting nanomedicine displayed good encapsulation efficiency, serum stability, drug release profile, and blood-brain barrier-penetration capability. Furthermore, NPD potently induced tau clearance in both cultured neuronal cells and the brains of AD mice. Moreover, intravenous injection of NPD led to a significant improvement in the cognitive function of the AD mice, without any remarkable abnormalities, thereby supporting its clinical development. Collectively, the novel nanomedicine developed in this study may serve as an innovative strategy for AD therapy, since it effectively and specifically induces tau protein clearance in brain lesions, which in turn enhances cognition.

摘要

阿尔茨海默病(AD)给全球经济和医疗保健系统带来了沉重负担。尽管AD的病理生理学仍存在争议,但其进展与tau蛋白聚集体的积累密切相关。因此,从脑损伤中清除tau蛋白可能是一种有前景的AD治疗策略。为了实现这一目标,本研究将蛋白水解靶向嵌合体(PROTAC)(一种通过泛素-蛋白酶体系统介导靶蛋白降解的新型蛋白质降解技术)与具有高血脑屏障穿透活性的神经递质衍生脂质体(NT-脂质体)纳米颗粒递送系统相结合,生成了一种名为NPD的新型纳米药物。使用DNA嵌入技术将阳离子型tau靶向PROTAC肽1负载到带正电荷的纳米颗粒上。所得纳米药物表现出良好的包封效率、血清稳定性、药物释放特性和血脑屏障穿透能力。此外,NPD在培养的神经元细胞和AD小鼠大脑中均能有效诱导tau蛋白清除。此外,静脉注射NPD可显著改善AD小鼠的认知功能,且无任何明显异常,从而支持其临床开发。总的来说,本研究中开发的新型纳米药物可能是一种创新的AD治疗策略,因为它能有效且特异性地诱导脑损伤中的tau蛋白清除,进而增强认知能力。

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