| Literature DB >> 31663118 |
Shouchao Wei1, Wanjuan Peng1, Yingren Mai1, Kanglan Li1, Wei Wei2, Li Hu1, Shaoping Zhu1, Haihong Zhou1, Wanxin Jie1, Zhuangsheng Wei1, Chenyao Kang1, Ruikai Li1, Zhou Liu1, Bin Zhao1, Zhiyou Cai3.
Abstract
Outer membrane vesicles (OMVs) are nanosized vesicles produced by the gut microbiota (GM). The GM is well-known to be involved in the pathological process of Alzheimer's disease (AD). However, the mechanism of OMVs is not clear. In the present study, we demonstrated the involvement of OMVs in the development of cognitive (learning and memory) dysfunction induced by blood-brain barrier (BBB) disruption. More important, further study showed that OMVs induced tau phosphorylation by activating glycogen synthase kinase 3β (GSK-3β) in the hippocampus. OMVs activated astrocytes and microglia, increased secretion of inflammatory cytokines (nuclear factor κB, interleukin-1β, and tumour necrosis factor-α) in the hippocampus. Therefore, OMVs increase the permeability of the BBB and promote the activation of astrocytes and microglia, inducing an inflammatory response and tau hyperphosphorylation by activating the GSK-3β pathway and finally leading to cognitive impairment.Entities:
Keywords: Alzheimer's disease; astrocytes; blood-brain barrier; glycogen synthase kinase 3β; gut microbiota; inflammatory cytokines; interleukin-1β; microglia; nuclear factor κB; outer membrane vesicles; tau; tumour necrosis factor-α
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Year: 2019 PMID: 31663118 DOI: 10.1002/jcp.29362
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384