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肾缺血再灌注损伤模型中长链非编码RNA的表达分析

Expression analysis of long non-coding RNAs in a renal ischemia-reperfusion injury model.

作者信息

Tao Qiu, Tianyu Wang, Jiangqiao Zhou, Zhongbao Chen, Xiaoxiong Ma, Long Zhang, Jilin Zou

机构信息

PhD, Department of Organ Transplantation, Renmin Hospital, Wuhan University, Hubei, China. Conception and design of the study, acquisition and analysis of data, manuscript writing.

PhD, Department of Organ Transplantation, Renmin Hospital, Wuhan University, Hubei, China. Design and supervised all phases of the study.

出版信息

Acta Cir Bras. 2019 Apr 29;34(4):e201900403. doi: 10.1590/s0102-865020190040000003.

Abstract

PURPOSE

To investigate the long non-coding RNAs (lncRNAs) profile on renal ischemia reperfusion in a mouse model.

METHODS

Microarray analysis was used to study the expression of misregulated lncRNA in a mouse model of renal ischemia reperfusion(I/R) with long ischemia time. Quantitative real-time PCR (qPCR) was used to verify the expression of selected lncRNAs and mRNAs.The potential functions of the lncRNA was analyzed by bioinformatics tools and databases.

RESULTS

Kidney function was impaired in I/R group compared to the normal group. Analysis showed that a total of 2267 lncRNAs and 2341 messenger RNAs (mRNAs) were significantly expressed in I/R group (≥2.0-fold, p < 0.05).The qPCR result showed that lncRNAs and mRNAs expression were consistent with the microarray analysis. The co-expression network profile analysis based on five validated lncRNAs and 203 interacted mRNAs showed it existed a total of 208 nodes and 333 connections. The GO and KEEG pathway analysis results showed that multiple lncRNAs are involved the mechanism of I/R.

CONCLUSION

Multiple lncRNAs are involved in the mechanism of I/R.These analysis results will help us to further understand the mechanism of I/R and promote the new methods targeted at lncRNA to improve I/R injury.

摘要

目的

研究小鼠肾缺血再灌注模型中的长链非编码RNA(lncRNA)谱。

方法

采用微阵列分析研究长缺血时间的小鼠肾缺血再灌注(I/R)模型中失调lncRNA的表达。运用定量实时聚合酶链反应(qPCR)验证所选lncRNA和mRNA的表达。通过生物信息学工具和数据库分析lncRNA的潜在功能。

结果

与正常组相比,I/R组的肾功能受损。分析显示,I/R组共有2267个lncRNA和2341个信使核糖核酸(mRNA)显著表达(≥2.0倍,p<0.05)。qPCR结果表明lncRNA和mRNA的表达与微阵列分析一致。基于5个验证的lncRNA和203个相互作用的mRNA的共表达网络谱分析显示,共有208个节点和333个连接。基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路分析结果表明,多个lncRNA参与了I/R的机制。

结论

多个lncRNA参与了I/R的机制。这些分析结果将有助于我们进一步了解I/R的机制,并推动针对lncRNA的新方法来改善I/R损伤。

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