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MicroRNA-135b alleviates MPP+-mediated Parkinson’s disease in in vitro model through suppressing FoxO1-induced NLRP3 inflammasome and pyroptosis

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成果类型:
期刊论文
作者:
Zeng, Rong;Luo, Di-Xian;Li, Hai-Peng;Zhang, Qi-Shan;Lei, Sheng-Suo;...
通讯作者:
Chen, Ji-Hua
作者机构:
[Zhang, Qi-Shan; Li, Hai-Peng; Zeng, Rong; Lei, Sheng-Suo; Chen, Ji-Hua] Chenzhou 1 Peoples Hosp, Dept Neurol, 102 Luojiajing, Chenzhou 423000, Hunan, Peoples R China.
[Luo, Di-Xian] Univ South China, Inst Translat Med, Hengyang 421001, Peoples R China.
通讯机构:
[Chen, Ji-Hua] C
Chenzhou 1 Peoples Hosp, Dept Neurol, 102 Luojiajing, Chenzhou 423000, Hunan, Peoples R China.
语种:
英文
关键词:
Caspase-1;FoxO1;NLRP3;Parkinson's disease;Pyroptosis;miRNA-135b
期刊:
Journal of Clinical Neuroscience
ISSN:
0967-5868
年:
2019
卷:
65
页码:
125-133
基金类别:
This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
机构署名:
本校为其他机构
院系归属:
医学院
摘要:
The present study focused on the novel roles and the underlying mechanisms of miR-135b in pyroptosis of MPP+-induced Parkinson's disease (PD). We established an in vitro PD model induced by MPP+. Our results demonstrated miR-135b was lower while FoxO1 was inversely higher in MPP+-treated SH-SY5Y and PC-12 cells. Luciferase reporter assay showed FoxO1 was a downstream target of miR-135b. MiR-135b mimics suppressed MPP+-induced pyroptosis and the upregulation of TXNIP, NLRP3, Caspase-1, ASC, GSDMD(Nterm) and IL-1 beta. Moreover, FoxO1 overexpression had no effect on miR-135b but reversed its own...

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