Liver transcriptomics reveals microRNA features of the host response in a mouse model of dengue virus infection

登革热 登革热病毒 小RNA 生物 Wnt信号通路 病毒 PI3K/AKT/mTOR通路 深度测序 转录组 免疫系统 免疫学 病毒学 基因 信号转导 基因表达 细胞生物学 遗传学 基因组
作者
Wenjiang Zheng,Ting Wang,Chengxin Liu,Qian Yan,Shaofeng Zhan,Geng Li,Xiaohong Liu,Yong Jiang
出处
期刊:Computers in Biology and Medicine [Elsevier BV]
卷期号:150: 106057-106057 被引量:2
标识
DOI:10.1016/j.compbiomed.2022.106057
摘要

Organ dysfunction, especially liver injury, caused by dengue virus (DENV) infection has been associated with fatal cases in dengue patients around the world. However, the pathophysiological mechanisms of liver involvement in dengue remain unclear. There is accumulating evidence that miRNAs are playing an important role in regulating viral pathogenesis, and it can help in diagnostic and anti-viral therapies development.We collected liver tissues of DENV-infected for small RNA sequencing to identify significantly different express miRNAs during dengue virus infection, and the identified target genes of these miRNAs were annotated by biological function and pathway enrichment.31 significantly altered miRNAs were identified, including 16 up-regulated and 15 down-regulated miRNAs. By performing a series of miRNA prediction and signaling pathway enrichment analyses, the down-regulated miRNAs of mmu-miR-484, mmu-miR-1247-5p and mmu-miR-6538 were identified to be the crucial miRNAs. Further analysis revealed that the inflammation and immune responses involving Hippo, PI3K-Akt, MAPK, Wnt, mTOR, TGF-beta, Tight junction, and Platelet activation were modulated collectively by these three key miRNAs during DENV infection. These pathways are considered to be closely associated with the pathogenic mechanism and treatment strategy of dengue patients.The miRNAs identified by sequencing, especially miR-484 may be the potential therapeutic targets for liver involvement in dengue patients which involves the regulation of vascular permeability and expression of inflammatory cytokines.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Dr_Stars完成签到,获得积分10
刚刚
1秒前
cwx完成签到,获得积分10
1秒前
ymh完成签到,获得积分10
1秒前
陶醉的蜜蜂完成签到 ,获得积分10
1秒前
SYLH应助研友_8KAOBn采纳,获得10
1秒前
1秒前
华仔应助泡泡糖采纳,获得10
1秒前
szz完成签到,获得积分10
2秒前
阿兰吉约丹完成签到,获得积分20
2秒前
3秒前
YY发布了新的文献求助10
3秒前
4秒前
无限雨南发布了新的文献求助20
4秒前
4秒前
hugoidea发布了新的文献求助10
5秒前
5秒前
现实的迎夏完成签到 ,获得积分10
5秒前
5秒前
三七发布了新的文献求助10
6秒前
6秒前
CodeCraft应助YY采纳,获得10
7秒前
科研通AI2S应助LC2228采纳,获得10
7秒前
谷谷发布了新的文献求助10
7秒前
8秒前
KK完成签到 ,获得积分10
8秒前
8秒前
良辰美景完成签到 ,获得积分10
8秒前
邝边边完成签到,获得积分10
8秒前
wantmygo完成签到,获得积分10
9秒前
车大花发布了新的文献求助10
9秒前
你香发布了新的文献求助10
9秒前
10秒前
引子完成签到,获得积分10
10秒前
linkman发布了新的文献求助10
10秒前
脑洞疼应助开心采纳,获得10
11秒前
上官若男应助了了采纳,获得20
11秒前
小胖墩完成签到,获得积分10
11秒前
科目三应助DrWang采纳,获得10
11秒前
12秒前
高分求助中
【提示信息,请勿应助】关于scihub 10000
A new approach to the extrapolation of accelerated life test data 1000
徐淮辽南地区新元古代叠层石及生物地层 500
Coking simulation aids on-stream time 450
康复物理因子治疗 400
北师大毕业论文 基于可调谐半导体激光吸收光谱技术泄漏气体检测系统的研究 390
Phylogenetic study of the order Polydesmida (Myriapoda: Diplopoda) 370
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 4016497
求助须知:如何正确求助?哪些是违规求助? 3556675
关于积分的说明 11322036
捐赠科研通 3289416
什么是DOI,文献DOI怎么找? 1812458
邀请新用户注册赠送积分活动 888053
科研通“疑难数据库(出版商)”最低求助积分说明 812060