Dipartimento di Biologia, Università degli Studi di Padova, Padova, Italy.
PLoS One. 2012;7(2):e31293. doi: 10.1371/journal.pone.0031293. Epub 2012 Feb 9.
Ionizing radiation (IR) can be extremely harmful for human cells since an improper DNA-damage response (DDR) to IR can contribute to carcinogenesis initiation. Perturbations in DDR pathway can originate from alteration in the functionality of the microRNA-mediated gene regulation, being microRNAs (miRNAs) small noncoding RNA that act as post-transcriptional regulators of gene expression. In this study we gained insight into the role of miRNAs in the regulation of DDR to IR under microgravity, a condition of weightlessness experienced by astronauts during space missions, which could have a synergistic action on cells, increasing the risk of radiation exposure.
METHODOLOGY/PRINCIPAL FINDINGS: We analyzed miRNA expression profile of human peripheral blood lymphocytes (PBL) incubated for 4 and 24 h in normal gravity (1 g) and in modeled microgravity (MMG) during the repair time after irradiation with 0.2 and 2Gy of γ-rays. Our results show that MMG alters miRNA expression signature of irradiated PBL by decreasing the number of radio-responsive miRNAs. Moreover, let-7i*, miR-7, miR-7-1*, miR-27a, miR-144, miR-200a, miR-598, miR-650 are deregulated by the combined action of radiation and MMG. Integrated analyses of miRNA and mRNA expression profiles, carried out on PBL of the same donors, identified significant miRNA-mRNA anti-correlations of DDR pathway. Gene Ontology analysis reports that the biological category of "Response to DNA damage" is enriched when PBL are incubated in 1 g but not in MMG. Moreover, some anti-correlated genes of p53-pathway show a different expression level between 1 g and MMG. Functional validation assays using luciferase reporter constructs confirmed miRNA-mRNA interactions derived from target prediction analyses.
CONCLUSIONS/SIGNIFICANCE: On the whole, by integrating the transcriptome and microRNome, we provide evidence that modeled microgravity can affects the DNA-damage response to IR in human PBL.
电离辐射(IR)对人类细胞可能极其有害,因为对 IR 的不适当 DNA 损伤反应(DDR)可能有助于致癌作用的启动。DDR 途径的干扰可能源于 miRNA 介导的基因调控功能的改变,miRNA 是一种小的非编码 RNA,作为基因表达的转录后调节剂。在这项研究中,我们深入了解了 miRNA 在模拟微重力下对 IR 的 DDR 调节中的作用,模拟微重力是宇航员在太空任务中经历的失重状态,这可能对细胞产生协同作用,增加辐射暴露的风险。
方法/主要发现:我们分析了人外周血淋巴细胞(PBL)在正常重力(1 g)和模拟微重力(MMG)下培养 4 和 24 小时后,在照射 0.2 和 2Gy γ射线后的修复时间内的 miRNA 表达谱。我们的结果表明,MMG 通过减少放射性反应 miRNA 的数量来改变受照射 PBL 的 miRNA 表达特征。此外,let-7i*、miR-7、miR-7-1*、miR-27a、miR-144、miR-200a、miR-598、miR-650 受到辐射和 MMG 的联合作用而失调。对同一供体的 PBL 进行 miRNA 和 mRNA 表达谱的综合分析,确定了 DDR 途径的显著 miRNA-mRNA 反相关。GO 分析报告说,当 PBL 在 1 g 下孵育时,“对 DNA 损伤的反应”的生物学类别是丰富的,但在 MMG 中则不是。此外,p53 途径的一些反相关基因在 1 g 和 MMG 之间显示出不同的表达水平。使用荧光素酶报告基因构建体的功能验证实验证实了从靶标预测分析得出的 miRNA-mRNA 相互作用。
结论/意义:总之,通过整合转录组和 microRNome,我们提供了证据表明,模拟微重力可以影响人类 PBL 对 IR 的 DNA 损伤反应。