Identification of microRNA-target genes in mice hippocampus at 1 week after pilocarpine-induced status epilepticus

被引:2
作者
Xiao, Xin-Li [1 ,3 ]
Wu, Xiao-Lin [1 ]
Tong, Hua [2 ]
Tan, Jing [2 ]
Liu, Le-Fan [4 ]
Si, Kai-Wei [5 ]
Peng-Bo-Yang [1 ]
Ma, Yan-Bing [1 ]
Zhou, Jin-Song [1 ]
Liu, Jian-Xin [2 ,3 ]
机构
[1] Xi An Jiao Tong Univ, Sch Basic Med Sci, Dept Human Anat Histol & Embryol, Hlth Sci Ctr, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Basic Med Sci, Inst Neurobiol, Hlth Sci Ctr, Xian 710061, Shaanxi, Peoples R China
[3] Xi An Jiao Tong Univ, Translat Med Inst, Dept Neurosci, Hlth Sci Ctr, 76 West Yanta Rd, Xian 710061, Peoples R China
[4] Hubei Univ Chinese Med, Sch Lab Med, 16 West Huangjiahu Rd, Wuhan 430065, Peoples R China
[5] Xi An Jiao Tong Univ, Sch Basic Med Sci, Hlth Sci Ctr, Dept Pathogen Biol & Immunol, Xian 710061, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Epilepsy; Status epilepticus; Hippocampus; Gene ontology; miRNA expression profiles; THYROTROPIN-RELEASING-HORMONE; TEMPORAL-LOBE EPILEPSY; EXPRESSION; MODEL;
D O I
10.1016/j.bbrc.2020.06.125
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNA) are believed to play a crucial role in the cause and treatment of temporal lobe epilepsy (TLE) by controlling gene expression in different stages of the disease. To investigate role of miRNA in the latent stage following status epilepticus, we first compared microRNA expression profiles in mice hippocampus at 1 week after pilocarpine-induced status epilepticus (SE) vs. controls in hippocampal tissues using Exiqon miRCURY LNA (TM) miRNAs Array. Then, the target genes of altered miRNAs were predicted using both TargetScan 7.1 and miRDB V5, and were further selected by intersecting with another independent mRNA expression profile dataset from the samples at the same time point. We found out 14 common genes as down miRNA target (up-mRNA) and 4 common genes as up miRNA target (down mRNA) in SE mice. miR-669m-3p-TRHR (thyrotropin releasing hormone receptor), miR-669m-3p-B3galt2 (beta-1,3-Galactosyltransferase 2), miR-105-PDPN (Podoplanin) and miR-883b-3p-CLEC-2 (C-typelectin-like-2) were found to be potential molecular mechanisms to modulate the calcium signaling pathway, glycosylation pathways and chemokine mediated inflammatory processes in mice hippocampus at 1 week after pilocarpine-induced SE, respectively. Our results offered potential novel insights into the cellular events in the mice hippocampus mediated by miRNASs-target genes that shape SE-evoked epileptogenesis. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:275 / 281
页数:7
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