α-synuclein accumulation in SH-SY5Y cell impairs autophagy in microglia by exosomes overloading miR-19a-3p

被引:44
|
作者
Zhou, Tianen [1 ]
Lin, Danyu [2 ]
Chen, Ying [3 ]
Peng, Sudan [3 ]
Jing, Xiuna [3 ]
Lei, Ming [3 ]
Tao, Enxiang [3 ]
Liang, Yanran [3 ]
机构
[1] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Emergency, Guangzhou 510120, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 8, Dept Neurol, Shenzhen 518033, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Neurol, Guangzhou 510120, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
AKT; autophagy; exosome; microglia; miR-19a-3p; mTOR; Parkinson's disease; PTEN; SH-SY5Y cell; alpha-synuclein; PARKINSONS-DISEASE; REGULATES AUTOPHAGY; EXPRESSION; DEGRADATION; NETWORKS; DEMENTIA; ATROPHY; ATG16L1;
D O I
10.2217/epi-2019-0222
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Aims: To reveal whether miRNAs in exosomes from alpha-synuclein transgenic SH-SY5Y cells are able to regulate autophagy in recipient microglia. Materials & methods: Microarray analysis and experimental verification were adopted to assess the significance of autophagy-associated miRNAs in exosomes from neuronal model of alpha-synucleinopathies. Results: We found that miR-19a-3p increased remarkably in the exosomes from alpha-synuclein gene transgenic SH-SY5Y cells. Further study inferred that alpha-synuclein gene transgenic SH-SY5Y cell-derived exosomes and miR-19a-3p mimic consistently inhibited the expression of phosphatase and tensin homolog and increased the phosphorylation of AKT and mTOR, both of which ultimately lead to the dysfunction of autophagy in recipient microglia. Conclusion: The data suggested that enhanced expression of miR-19a-3p in exosomes suppress autophagy in recipient microglia by targeting the phosphatase and tensin homolog/AKT/mTOR signaling pathway.
引用
收藏
页码:1661 / 1677
页数:17
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