Comprehensive Analysis of lncRNAs, miRNAs and mRNAs in Mouse Hippocampus With Hepatic Encephalopathy

被引:6
|
作者
Zhang, Huijie [1 ,2 ]
Zhang, Wenjun [1 ,3 ]
Yu, Guangyin [1 ]
Li, Fang [1 ]
Hui, Yuqing [1 ,2 ]
Cha, Shuhan [1 ]
Chen, Meiying [1 ]
Zhu, Wei [1 ]
Zhang, Jifeng [1 ]
Guo, Guoqing [1 ]
Gong, Xiaobing [1 ,2 ]
机构
[1] Jinan Univ, Dept Anat, Neurosci Lab Cognit & Dev Disorders, Med Coll, Guangzhou, Peoples R China
[2] Jinan Univ, Dept Gastroenterol, Affiliated Hosp 1, Guangzhou, Peoples R China
[3] Jinan Univ, Nursing Sch, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
hepatic encephalopathy; long non-coding RNA; microRNA; Six3os1; AQP1; cognitive function; CERNA; IMPAIRMENT;
D O I
10.3389/fgene.2022.868716
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Hepatic encephalopathy (HE) often presents with varying degrees of cognitive impairment. However, the molecular mechanism of its cognitive impairment has not been fully elucidated. Whole transcriptome analysis of hippocampus between normal and HE mice was performed by using RNA sequencing. 229 lncRNAs, 49 miRNAs and 363 mRNAs were differentially expressed in HE mice. The lncRNA-miRNA-mRNA interaction networks were established, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were performed. Dysregulated RNAs in interaction networks were mainly involved in synaptic plasticity and the regulation of learning and memory. In NH4Cl-treated hippocampal neurons, the dendritic spine density and maturity decreased significantly, the amplitude and frequency of mIPSC increased, while the amplitude and frequency of mEPSC decreased. These manifestations can be reversed by silencing SIX3OS1. Further research on these no-coding RNAs may lead to new therapies for the treatment and management of brain dysfunction caused by HE.
引用
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页数:15
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