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Burns. 2016 Mar;42(2):405-13. doi: 10.1016/j.burns.2015.06.015. Epub 2015 Dec 29.
3
[Screening genes related with leukocyte responses early after burn injury: analysis of differentially gene expression profiling data in mice].[烧伤后早期与白细胞反应相关基因的筛选:小鼠差异基因表达谱数据分析]
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Retraction note: Gene expression profiling analysis of the putamen for the investigation of compensatory mechanisms in Parkinson's disease.撤稿说明:对壳核进行基因表达谱分析以研究帕金森病的代偿机制。
BMC Neurol. 2015 Mar 26;15:45. doi: 10.1186/s12883-015-0307-3.
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CDK1 plays an important role in the maintenance of pluripotency and genomic stability in human pluripotent stem cells.细胞周期蛋白依赖性激酶1(CDK1)在人类多能干细胞的多能性维持和基因组稳定性方面发挥着重要作用。
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Nucleic Acids Res. 2013 Jan;41(Database issue):D808-15. doi: 10.1093/nar/gks1094. Epub 2012 Nov 29.
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Burn injury triggered dysfunction in dendritic cell response to TLR9 activation and resulted in skewed T cell functions.烧伤损伤触发树突状细胞对 TLR9 激活反应的功能障碍,并导致 T 细胞功能的偏倚。
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9
The composition and signaling of the IL-35 receptor are unconventional.IL-35 受体的组成和信号传导是非传统的。
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10
Burn-induced alterations in toll-like receptor-mediated responses by bronchoalveolar lavage cells.烟雾吸入性损伤对支气管肺泡灌洗液中 Toll 样受体介导反应的影响。
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[通过差异基因表达谱筛选小鼠烧伤后早期与白细胞反应相关的生物标志物]

[Screening of biomarkers related with leukocyte responses early after burn injury in mice by differential gene expression profiling].

作者信息

Zou Qiong, Gao Yan-Bin, Jin Hui, Lu Zhi-Yang, Shi Peng-Wei, Yang Lei

机构信息

Department of Burns, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. E-mail:

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2017 Jun 20;37(6):767-773. doi: 10.3969/j.issn.1673-4254.2017.06.09.

DOI:10.3969/j.issn.1673-4254.2017.06.09
PMID:28669950
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6744150/
Abstract

OBJECTIVE

To screen the genes related with leukocyte responses in mice early after burn injury by bioinformatic analysis of the gene expression profiling data.

METHODS

The gene expression profiles were obtained from GEO (GSE7404, Mouse musculus, 25% TBSA, full-thickness) database. T test, fold changes and GO functional enrichment analysis were used to identify the differentially expressed genes (DEGs) related to leukocyte responses to burns; the interacting genes were transferred to STRING to construct the protein-protein interaction (PPI) network. Biological annotation of the sub-networks was executed using the software Cytoscape. Real-time PCR and Western blotting were used to verify the DEGs in mice.

RESULTS

In mice at 1 day post-burn, a total of 658 genes were up-regulated and 1167 were down-regulated. PPI network and module analysis suggested that some of the genes (Stat1, Cdk1, Cd19, Lck and Jun) may play critical roles in the PPI network post-burn. Real-time PCR and Western blotting results in mice were consistent with those of bioinformatic analysis of Stat1, Cdk1 and Jun.

CONCLUSION

Stat1, Cdk1 and Jun might be critical players in the development of leukocyte response in mice early after burn injury. Our finding provides new insights into the pathogenesis of leukocyte response to burn injury and identifies several biomarkers as potential targets for burn treatment.

摘要

目的

通过对基因表达谱数据进行生物信息学分析,筛选烧伤后早期小鼠白细胞反应相关基因。

方法

从基因表达综合数据库(GEO,GSE7404,小家鼠,25% 体表面积,全层烧伤)获取基因表达谱。采用t检验、倍数变化及基因本体(GO)功能富集分析来鉴定与烧伤后白细胞反应相关的差异表达基因(DEG);将相互作用基因导入STRING构建蛋白质 - 蛋白质相互作用(PPI)网络。使用Cytoscape软件对子网进行生物学注释。采用实时定量PCR和蛋白质免疫印迹法验证小鼠中的DEG。

结果

在烧伤后1天的小鼠中,共有658个基因上调,1167个基因下调。PPI网络和模块分析表明,部分基因(Stat1、Cdk1、Cd19、Lck和Jun)可能在烧伤后的PPI网络中起关键作用。小鼠的实时定量PCR和蛋白质免疫印迹结果与Stat1、Cdk1和Jun的生物信息学分析结果一致。

结论

Stat1、Cdk1和Jun可能是烧伤后早期小鼠白细胞反应发生过程中的关键参与者。我们的发现为烧伤后白细胞反应的发病机制提供了新见解,并鉴定出几种生物标志物作为烧伤治疗的潜在靶点。