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整合大鼠肺辐射损伤后微小RNA和信使核糖核酸的表达谱

Integrating microRNA and mRNA expression profiles in response to radiation-induced injury in rat lung.

作者信息

Xie Ling, Zhou Jundong, Zhang Shuyu, Chen Qing, Lai Rensheng, Ding Weiqun, Song ChuanJun, Meng XingJun, Wu Jinchang

机构信息

Department of Radio-oncology, Nanjing Medical University Affiliated Suzhou Hospital, Suzhou 215001, China.

出版信息

Radiat Oncol. 2014 May 9;9:111. doi: 10.1186/1748-717X-9-111.

Abstract

PURPOSE

Exposure to radiation provokes cellular responses, which are likely regulated by gene expression networks. MicroRNAs are small non-coding RNAs, which regulate gene expression by promoting mRNA degradation or inhibiting protein translation. The expression patterns of both mRNA and miRNA during the radiation-induced lung injury (RILI) remain less characterized and the role of miRNAs in the regulation of this process has not been studied. The present study sought to evaluate miRNA and mRNA expression profiles in the rat lung after irradiation.

METHODS AND MATERIALS

Male Wistar rats were subjected to single dose irradiation with 20 Gy using 6 MV x-rays to the right lung. (A dose rate of 5 Gy/min was applied). Rats were sacrificed at 3, 12 and 26 weeks after irradiation, and morphological changes in the lung were examined by haematoxylin and eosin. The miRNA and mRNA expression profiles were evaluated by microarrays and followed by quantitative RT-PCR analysis.

RESULTS

A cDNA microarray analysis found 2183 transcripts being up-regulated and 2917 transcripts down-regulated (P ≤ 0.05, ≥2.0 fold change) in the lung tissues after irradiation. Likewise, a miRNAs microarray analysis indicated 15 miRNA species being up-regulated and 8 down-regulated (P ≤ 0.05). Subsequent bioinformatics analyses of the differentially expressed mRNA and miRNAs revealed that alterations in mRNA expression following irradiation were negatively correlated with miRNAs expression.

CONCLUSIONS

Our results provide evidence indicating that irradiation induces alterations of mRNA and miRNA expression in rat lung and that there is a negative correlation of mRNA and miRNA expression levels after irradiation. These findings significantly advance our understanding of the regulatory mechanisms underlying the pathophysiology of radiation-induced lung injury. In summary, RILI does not develop gradually in a linear process. In fact, different cell types interact via cytokines in a very complex network. Furthermore, this study suggests that microRNAs may serve an important role in the pathogenesis of RILI and that understanding their role in RILI may have a significant effect on patient management and diagnosis in the future.

摘要

目的

暴露于辐射会引发细胞反应,这些反应可能受基因表达网络调控。微小RNA是一类小的非编码RNA,通过促进mRNA降解或抑制蛋白质翻译来调控基因表达。辐射诱导的肺损伤(RILI)过程中mRNA和miRNA的表达模式仍不太清楚,且miRNA在该过程调控中的作用尚未得到研究。本研究旨在评估照射后大鼠肺中miRNA和mRNA的表达谱。

方法和材料

雄性Wistar大鼠右肺接受单次20 Gy的6 MV X射线照射(剂量率为5 Gy/min)。照射后3周、12周和26周处死大鼠,用苏木精和伊红染色检查肺的形态变化。通过微阵列评估miRNA和mRNA的表达谱,随后进行定量RT-PCR分析。

结果

cDNA微阵列分析发现,照射后肺组织中有2183个转录本上调,2917个转录本下调(P≤0.05,变化倍数≥2.0)。同样,miRNA微阵列分析表明有15种miRNA上调,8种下调(P≤0.05)。随后对差异表达的mRNA和miRNA进行生物信息学分析发现,照射后mRNA表达的改变与miRNA表达呈负相关。

结论

我们的结果提供了证据,表明照射可诱导大鼠肺中mRNA和miRNA表达的改变,且照射后mRNA和miRNA表达水平呈负相关。这些发现显著推进了我们对辐射诱导肺损伤病理生理学潜在调控机制的理解。总之,RILI并非以线性过程逐渐发展。实际上,不同细胞类型通过细胞因子在一个非常复杂的网络中相互作用。此外,本研究表明微小RNA可能在RILI的发病机制中起重要作用,了解它们在RILI中的作用可能对未来患者的管理和诊断产生重大影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b527/4044330/d6f7e7f838ac/1748-717X-9-111-1.jpg

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