Ma Mengmeng, Gao Nan, Li Xuexia, Liu Zhenqi, Pi Zifeng, Du Xiubo, Ren Jinsong, Qu Xiaogang
Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China.
University of Science and Technology of China, Hefei, Anhui 230029, China.
ACS Nano. 2020 Aug 25;14(8):9894-9903. doi: 10.1021/acsnano.0c02733. Epub 2020 Jul 30.
Phototherapy, such as photodynamic therapy and photothermal therapy, holds great potential for modulation of Alzheimer's β-amyloid (Aβ) self-assembly. Unfortunately, current works for phototherapy of Alzheimer's disease (AD) are just employing either visible or first near-infrared (NIR-I) light with limited tissue penetration, which can not avoid damaging nearby normal tissues of AD patients through the dense skull and scalp. To overcome the shortcomings of AD phototherapy, herein we report an amyloid targeting, N-doped three-dimensional mesoporous carbon nanosphere (KD8@N-MCNs) as a second near-infrared (NIR-II) PTT agent. This makes it possible for photothermal dissociation of Aβ aggregates through the scalp and skull in a NIR-II window without hurting nearby normal tissues. Besides, KD8@N-MCNs have both superoxide dismutase and catalase activities, which can scavenge intracellular superfluous reactive oxygen species and alleviate neuroinflammation . Furthermore, KD8@N-MCNs efficiently cross the blood-brain barrier owing to the covalently grafted target peptides of KLVFFAED on the nanosphere surface. studies demonstrate that KD8@N-MCNs decrease Aβ deposits, ameliorate memory deficits, and alleviate neuroinflammation in the 3xTg-AD mouse model. Our work provides a biocompatible and non-invasive way to attenuate AD-associated pathology.
光疗法,如光动力疗法和光热疗法,在调节阿尔茨海默病β-淀粉样蛋白(Aβ)自组装方面具有巨大潜力。不幸的是,目前用于阿尔茨海默病(AD)光疗的研究仅采用可见光或第一近红外(NIR-I)光,组织穿透性有限,无法避免通过致密的头骨和头皮对AD患者附近的正常组织造成损伤。为了克服AD光疗的缺点,在此我们报道一种靶向淀粉样蛋白的N掺杂三维介孔碳纳米球(KD8@N-MCNs)作为第二近红外(NIR-II)光热疗法试剂。这使得在NIR-II窗口内通过头皮和头骨对Aβ聚集体进行光热解离成为可能,而不会伤害附近的正常组织。此外,KD8@N-MCNs同时具有超氧化物歧化酶和过氧化氢酶活性,能够清除细胞内多余的活性氧并减轻神经炎症。此外,由于纳米球表面共价接枝了KLVFFAED靶向肽,KD8@N-MCNs能够有效穿过血脑屏障。研究表明,在3xTg-AD小鼠模型中,KD8@N-MCNs减少了Aβ沉积,改善了记忆缺陷,并减轻了神经炎症。我们的工作提供了一种生物相容且非侵入性的方法来减轻AD相关病理。