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Exosomes Isolated From Human Umbilical Cord Mesenchymal Stem Cells Alleviate Neuroinflammation and Reduce Amyloid-Beta Deposition by Modulating Microglial Activation in Alzheimer’s Disease

神经炎症 微泡 小胶质细胞 间充质干细胞 外体 医学 促炎细胞因子 脐带 免疫学 细胞生物学 炎症 生物 病理 小RNA 生物化学 基因
作者
Mao Ding,Yang Shen,Ping Wang,Zhaohong Xie,Shunliang Xu,Zhengyu Zhu,Yun Wang,Yongtao Lyu,Wang Dewei,Linlin Xu,Jianzhong Bi,Hui Yang
出处
期刊:Neurochemical Research [Springer Science+Business Media]
卷期号:43 (11): 2165-2177 被引量:272
标识
DOI:10.1007/s11064-018-2641-5
摘要

Alzheimer's disease (AD) is the most common neurodegenerative disease characterized by excessive accumulation of the amyloid-β peptide (Aβ) in the brain, which has been considered to mediate the neuroinflammation process. Microglial activation is the main component of neuroimmunoregulation. In recent years, exosomes isolated from human umbilical cord mesenchymal stem cells (hucMSC-exosomes) have been demonstrated to mimic the therapeutic effects of hucMSCs in many inflammation-related diseases. In this study, exosomes from the supernatant of hucMSCs were injected into AD mouse models. We observed that hucMSC-exosomes injection could repair cognitive disfunctions and help to clear Aβ deposition in these mice. Moreover, we found that hucMSC-exosomes injection could modulate the activation of microglia in brains of the mice to alleviated neuroinflammation. The levels of pro-inflammatory cytokines in peripheral blood and brains of mice were increased and the levels of anti-inflammatory cytokines were decreased. We also treated BV2 cells with hucMSC-exosomes in culture medium. HucMSC-exosomes also had inflammatory regulating effects to alternatively activate microglia and modulate the levels of inflammatory cytokines in vitro.
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