| Literature DB >> 29380367 |
Xin Wen1,2, Xin-Rui Han1,2, Yong-Jian Wang1,2, Shan Wang1,2, Min Shen1,2, Zi-Feng Zhang1,2, Shao-Hua Fan1,2, Qun Shan1,2, Liang Wang1,2, Meng-Qiu Li1,2, Bin Hu1,2, Chun-Hui Sun1,2, Dong-Mei Wu1,2, Jun Lu1,2, Yuan-Lin Zheng1,2.
Abstract
Epilepsy is a group of neurological disorders characterized by epileptic seizures. In this study, we aim to explore the role of microRNA-421 (miR-421) in hippocampal neurons of epilepsy mice via the TLR/MYD88 pathway. Forty mice were randomly served as the normal and model (established as epilepsy model) groups. Hippocampal neurons were assigned into seven groups with different transfections. The RT-qPCR and western blotting were conducted to examine the expression of miR-421 TLR2, TLR4, MYD88, Bax, Bcl-2, p53, Beclin-1, and LC3II/LC3I. Cell proliferation and apoptosis were detected by MTT and flow cytometry.MYD88 is a target gene of miR-421. Model mice showed elevated expression of TLR2, TLR4, MYD88, Bax, p53, Beclin-1, and LC3II/LC3I but reduced expression of miR-421 and Bcl-2. In vitro experiments reveals that overexpression of miR-421 inhibited the TLR/MYD88 pathway. Besides, overexpressed miR-421 declined cell apoptosis but increased cell proliferation. It reveals that miR-421 targeting MYD88 could inhibit the apoptosis and autophagy of hippocampal neurons in epilepsy mice by down-regulating the TLR/MYD88 pathway.Entities:
Keywords: TLR/MYD88 pathway; apoptosis; autophagy; epilepsy; hippocampal neurons; microRNA-421
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Year: 2018 PMID: 29380367 DOI: 10.1002/jcp.26498
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384