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MicroRNA-207 enhances radiation-induced apoptosis by directly targeting akt3 in cochlea hair cells

机译:MicroRNA-207通过直接靶向耳蜗毛细胞的AKT3增强辐射诱导的细胞凋亡

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摘要

MicroRNAs (miRNAs) have important roles in various types of cellular biological processes. Our study aimed to determine whether miRNAs function in the regulation of ionizing radiation (IR)-induced cell death in auditory cells and to determine how they affect the cellular response to IR. Microarray and qRT-PCR were performed to identify and confirm the differential expression of miRNAs in the cochlea hair cell line HEI-OC1 and in vivo after IR. Upregulation or downregulation of miRNAs using miRNA mimics or inhibitor were detected to characterize the biological effects of the indicated miRNAs. Bioinformatic analyses, luciferase reporter assays and mRNA knockdown were performed to identify a miRNA target gene. We determined that miR-207 was significantly upregulated after IR. MiR-207 enhances IR-induced apoptosis and DNA damage in HEI-OC1 cells. Furthermore, Akt3 was confirmed to be a direct target of miR-207. Downregulation of Akt3 mimics the effects of miR-207. MiR-207 enhances IR-induced apoptosis by directly targeting Akt3 and anti-miR-207 may have a potential role in protecting cochlea hair cells from IR.
机译:MicroRNA(miRNA)在各种类型的细胞生物过程中具有重要作用。我们的研究旨在确定miRNA是否在调节电离辐射(IR)诱导的听觉细胞中死亡并确定它们如何影响IR的细胞反应。进行微阵列和QRT-PCR以鉴定并确认MiRNA在耳蜗毛细胞系Hei-OC1和IR中的差异表达。使用miRNA模仿或抑制剂的上调或下调miRNA,以表征所指出的miRNA的生物学效应。进行生物信息分析,进行荧光素酶报告分析和mRNA敲低以鉴定miRNA靶基因。我们确定了IR-207之后明显上调。 miR-207增强了Hei-OC1细胞中的IR诱导的细胞凋亡和DNA损伤。此外,确认AKT3是miR-207的直接靶标。 AKT3的下调模仿miR-207的影响。 MIR-207通过直接靶向AKT3增强IR诱导的细胞凋亡,并且抗miR-207可具有保护耳蜗毛细胞的潜在作用。

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