Mo Lijun,Song Man,Liu Xiaodan,Guan Hua,Zhou Pingkun.Identification and bioinformatic function analysis of differentially expressed miRNAs in the exosomes secreted from BEP2D cells irradiated by γ-rays[J].Chinese Journal of Radiological Medicine and Protection,2018,38(7):481-488 |
Identification and bioinformatic function analysis of differentially expressed miRNAs in the exosomes secreted from BEP2D cells irradiated by γ-rays |
Received:May 02, 2018 |
DOI:10.3760/cma.j.issn.0254-5098.2018.07.001 |
KeyWords:γ-ray irradiation Exosomes miRNA Bioinformatics Bystander effect |
FundProject:国家自然科学基金(81530085) |
Author Name | Affiliation | E-mail | Mo Lijun | The School of Public Health, University of South China, Hengyang 421001, China | | Song Man | Beijing Key Laboratory for Radiobiology, Institute of Radiation Medicine, AMMS, Beijing 100850, China | | Liu Xiaodan | Beijing Key Laboratory for Radiobiology, Institute of Radiation Medicine, AMMS, Beijing 100850, China | | Guan Hua | Beijing Key Laboratory for Radiobiology, Institute of Radiation Medicine, AMMS, Beijing 100850, China | | Zhou Pingkun | Beijing Key Laboratory for Radiobiology, Institute of Radiation Medicine, AMMS, Beijing 100850, China | zhoupk@bmi.ac.cn |
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Abstract:: |
Objective To identify the differentially expressed miRNAs in the exosomes secreted from γ-ray irradiated cells and provide new clues in disclosing the mechanisms of radiation-induced bystander effects. Methods The human bronchial epithelial cells (BEP2D) were irradiated with 60Co γ-rays, and the exosomes were collected by ultracentrifugation from the culture medium of 2 Gy-irradiated cells and non-irradiated control. The exosomes were identified by an electron microscopy. The miRNA microarray technique was used to analyze the miRNA expression profiles in the exosomes. qRT-PCR was used to verify the miRNAs expression. The functional pathways of miRNAs targeting genes were predicted by informatic analysis using the databases of TargetScan, miRanda, GO and KEGG. Results Sixteen miRNA with significantly increased expression (P<0.05) were identified in the exosomes of BEP2D cells at 4 h post-2 Gy irradiation as compared with the non-irradiated control cells, among which miR-100-5p, miR-1246, miR-29b-3p, and miR-7-5p were further confirmed to be unregulated by qRT-PCR assay (P<0.05). Meanwhile, the expression changes of above-mentioned four miRNAs were also investigated in the irradiated cells. The data indicated the expression was significantly increased at 2 h post-2 Gy irradiation for the miR-100-5p, miR-1246, miR-29b-3p in addition to miR-7-5p. However, all these four miRNAs were downregulated in the cells at 4 h post-irradiation and then gradually recovered. Bioinformatics analysis showed that the targeted genes of these differentially expressed miRNAs might participate in the biological processes and signal pathways of cell adhesion, mTOR signal pathway, chromatin modification, HR and NHEJ pathways of DNA repair and so on. Conclusions Radiation-inducible miRNAs have been identified in the exosomes from the irradiated BEP2D cells. The target genes of these miRNAs play roles in a series of important biological processes and functional pathways, which provides new clues in elucidating the mechanisms of radiation-induced bystander effects. |
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