鼻内给药诱导多能干细胞衍生的皮层神经干细胞分泌组作为阿尔茨海默病的治疗选择。

IF 10.8 1区 医学 Q1 NEUROSCIENCES Translational Neurodegeneration Pub Date : 2023-11-09 DOI:10.1186/s40035-023-00384-8
Hyunkyung Mo, Juryun Kim, Jennifer Yejean Kim, Jang Woon Kim, Heeju Han, Si Hwa Choi, Yeri Alice Rim, Ji Hyeon Ju
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引用次数: 0

摘要

背景:阿尔茨海默病(AD)是老年人最常见的神经退行性疾病,导致认知能力逐渐受损。各种AD治疗方法的开发研究正在进行中;然而,目前还没有明确的治疗方法。在此,我们提出了诱导多能干细胞(iPSC)衍生的皮层神经干细胞分泌组(CNSC-SE)作为AD的一种新的候选治疗方法,并探索其疗效。方法:我们首先评估了CNSC-SE处理对皮层神经细胞分化过程中神经成熟和电磁信号的影响。然后,为了确认体内疗效,通过鼻腔向5×FAD小鼠模型施用CNSC-SE(5μg/g,每周一次,4周)。研究了细胞介导的对神经恢复、淀粉样蛋白β(Aβ)斑块聚集、脑中小胶质细胞和星形胶质细胞检测以及神经炎症反应的影响。iPSC衍生的CNSC-SE的代谢组学分析表明,它含有可以发挥神经保护作用或增强认知恢复作用的成分。结果:人iPSC衍生的CNSC-SE在体外增加了神经元增殖和树突结构的形成。此外,CNSC SE处理的iPSC衍生的皮层神经元获得了电网络活动和动作电位爆发。CNSC-SE处理的5×FAD小鼠表现出记忆恢复和Aβ斑块积聚减少。结论:我们的研究结果表明,iPSC衍生的CNSC-SE可能是AD减少淀粉样蛋白浸润和恢复记忆的一种潜在的非侵入性治疗选择。
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Intranasal administration of induced pluripotent stem cell-derived cortical neural stem cell-secretome as a treatment option for Alzheimer's disease.

Background: Alzheimer's disease (AD) is the most common neurodegenerative disorder in the elderly, resulting in gradual destruction of cognitive abilities. Research on the development of various AD treatments is underway; however, no definitive treatment has been developed yet. Herein, we present induced pluripotent stem cell (iPSC)-derived cortical neural stem cell secretome (CNSC-SE) as a new treatment candidate for AD and explore its efficacy.

Methods: We first assessed the effects of CNSC-SE treatment on neural maturation and electromagnetic signal during cortical nerve cell differentiation. Then to confirm the efficacy in vivo, CNSC-SE was administered to the 5×FAD mouse model through the nasal cavity (5 μg/g, once a week, 4 weeks). The cell-mediated effects on nerve recovery, amyloid beta (Aβ) plaque aggregation, microglial and astrocyte detection in the brain, and neuroinflammatory responses were investigated. Metabolomics analysis of iPSC-derived CNSC-SE revealed that it contained components that could exert neuro-protective effects or amplify cognitive restorative effects.

Results: Human iPSC-derived CNSC-SE increased neuronal proliferation and dendritic structure formation in vitro. Furthermore, CNSC-SE-treated iPSC-derived cortical neurons acquired electrical network activity and action potential bursts. The 5×FAD mice treated with CNSC-SE showed memory restoration and reduced Aβ plaque accumulation.

Conclusions: Our findings suggest that the iPSC-derived CNSC-SE may serve as a potential, non-invasive therapeutic option for AD in reducing amyloid infiltration and restoring memory.

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来源期刊
Translational Neurodegeneration
Translational Neurodegeneration Neuroscience-Cognitive Neuroscience
CiteScore
19.50
自引率
0.80%
发文量
44
审稿时长
10 weeks
期刊介绍: Translational Neurodegeneration, an open-access, peer-reviewed journal, addresses all aspects of neurodegenerative diseases. It serves as a prominent platform for research, therapeutics, and education, fostering discussions and insights across basic, translational, and clinical research domains. Covering Parkinson's disease, Alzheimer's disease, and other neurodegenerative conditions, it welcomes contributions on epidemiology, pathogenesis, diagnosis, prevention, drug development, rehabilitation, and drug delivery. Scientists, clinicians, and physician-scientists are encouraged to share their work in this specialized journal tailored to their fields.
期刊最新文献
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