Gene Expression Profile of Peripheral Blood Mononuclear Cells in Response to Intracerebral Hemorrhage

被引:12
|
作者
Sang, Ming [1 ]
Wang, Xuanbin [1 ]
Zhang, Hanyao [2 ]
Sun, Xiaodong [1 ]
Ding, Xudong [1 ]
Wang, Puqing [1 ]
Jiao, Rong [1 ]
Cheng, Huaxian [1 ]
Yang, Sijun [3 ,4 ]
Zhang, Guibin [1 ]
机构
[1] Hubei Univ Med, Cent Lab, Xiangyang Peoples Hosp 1, Inst Parkinsons Dis,Hubei Key Lab Wudang Local Ch, Shiyan 442000, Peoples R China
[2] Southwest Forestry Univ, Coll Forestry, Key Lab Biodivers Conservat Southwest China, Kunming, Yunnan, Peoples R China
[3] Wuhan Univ, Sch Med, Ctr Expt Anim, ABSL Lab 3, Wuhan 430071, Hubei, Peoples R China
[4] Wuhan Univ, Sch Med, State Key Lab Virol, Wuhan 430071, Hubei, Peoples R China
关键词
intracerebral hemorrhage; RNA-sequencing; peripheral blood mononuclear cells; GAMMA-GLUTAMYL-TRANSFERASE; ISCHEMIC-STROKE; BRAIN-BARRIER; DEATH; RISK; ACTIVATION; BIOMARKERS; INDUCTION; PROGNOSIS; PROGRESS;
D O I
10.1089/dna.2017.3650
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
RNA-sequencing, a powerful tool, yields a comprehensive view of whole transcriptome. Intracerebral hemorrhage (ICH) is a devastating form of stroke. To date, RNA-sequencing analysis of ICH has not been reported. Peripheral blood mononuclear cells (PBMCs) were used as a source of mRNA for gene expression profile analysis in stroke. In this study, we performed transcriptome analyses for PBMCs from four ICH patients and four healthy volunteers on Illumina platform. We identified 4040 significantly differentially expressed genes (DEGs). Functional annotation of DEGs with DAVID Bioinformatics Resources indicated that genes associated with cell apoptosis, autophagy, cell-cell adhesion, inflammatory response, protein binding, positive regulation of gene expression, and signal transduction were most significantly enriched by DEGs. Gene set enrichment analysis identified 40 significant Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, including chemokine signaling, cytokine-cytokine receptor interaction, oxidative phosphorylation, and glutathione metabolism processes. These data point to a complex mechanism for ICH pathogenesis. Overall, the present study demonstrated an altered gene expression profile of PBMCs in response to acute ICH. Our study provided important information for understanding the molecular mechanisms of ICH pathogenesis at system-wide levels.
引用
收藏
页码:647 / 654
页数:8
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