Department of Laboratory Medicine, The Third Xiangya Hospital, Central South University, No.138,Tongzipo Road,Yuelu District, Changsha, Hunan, 410013, China.
Department of Blood Transfusion, The Third Xiangya Hospital, Central South University, No.138,Tongzipo Road,Yuelu District, Changsha, Hunan, 410013, China.
Adv Sci (Weinh). 2023 Jun;10(18):e2301361. doi: 10.1002/advs.202301361. Epub 2023 Apr 19.
Alzheimer's disease (AD) is one of the most common neurodegenerative diseases in the elderly population. Despite significant advances in studies of the pathobiology on AD, there is still no effective treatment. Here, an erythrocyte membrane-camouflaged nanodrug delivery system (TR-ZRA) modified with transferrin receptor aptamers that can be targeted across the blood-brain barrier to ameliorate AD immune environment is established. Based on metal-organic framework (Zn-CA), TR-ZRA is loaded with CD22shRNA plasmid to silence the abnormally high expression molecule CD22 in aging microglia. Most importantly, TR-ZRA can enhance the ability of microglia to phagocytose Aβ and alleviate complement activation, which can promote neuronal activity and decrease inflammation level in the AD brain. Moreover, TR-ZRA is also loaded with Aβ aptamers, which allow rapid and low-cost monitoring of Aβ plaques in vitro. After treatment with TR-ZRA, learning, and memory abilities are enhanced in AD mice. In conclusion, the biomimetic delivery nanosystem TR-ZRA in this study provides a promising strategy and novel immune targets for AD therapy.
阿尔茨海默病(AD)是老年人中最常见的神经退行性疾病之一。尽管 AD 的病理生物学研究取得了重大进展,但仍没有有效的治疗方法。在这里,建立了一种转铁蛋白受体适体修饰的红细胞膜伪装纳米药物递送系统(TR-ZRA),该系统可以通过血脑屏障靶向改善 AD 免疫环境。基于金属有机骨架(Zn-CA),TR-ZRA 负载 CD22shRNA 质粒,沉默衰老小胶质细胞中异常高表达的分子 CD22。最重要的是,TR-ZRA 可以增强小胶质细胞吞噬 Aβ的能力,并减轻补体激活,从而促进 AD 大脑中的神经元活动并降低炎症水平。此外,TR-ZRA 还负载有 Aβ适体,可在体外实现对 Aβ斑块的快速、低成本监测。用 TR-ZRA 治疗后,AD 小鼠的学习和记忆能力得到增强。总之,本研究中的仿生递药纳米系统 TR-ZRA 为 AD 治疗提供了有前途的策略和新的免疫靶标。