| Literature DB >> 30259257 |
Mao Ding1, Yang Shen1, Ping Wang2, Zhaohong Xie2, Shunliang Xu2, ZhengYu Zhu2, Yun Wang2, Yongtao Lyu3, Dewei Wang2, Linlin Xu2, JianZhong Bi4, Hui Yang5.
Abstract
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.Entities:
Keywords: Alzheimer’s disease; Amyloid-β peptides; Exosomes; Human umbilical cord mesenchymal stem cells; Microglial activation; Neuroinflammation
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Year: 2018 PMID: 30259257 DOI: 10.1007/s11064-018-2641-5
Source DB: PubMed Journal: Neurochem Res ISSN: 0364-3190 Impact factor: 3.996