Department of Radiotherapy and Oncology, The Second Affiliated Hospital of Soochow University, Suzhou 215004, P R China.
Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Suzhou 215123, P R China.
Int J Biol Sci. 2017 Sep 21;13(10):1287-1296. doi: 10.7150/ijbs.18890. eCollection 2017.
This study investigated whether exosomal microRNA-7 (miR-7) mediates lung bystander autophagy after focal brain irradiation in mice. After 10 Gy or sham irradiation of mice brains, lung tissues were extracted for the detection of autophagy markers by immunohistochemistry, western blotting, and quantitative real-time reverse transcription PCR (qRT-PCR), meanwhile the brains were dissociated, the neuron/astrocyte/microglia/oligodendrocyte were isolated, and the miR-7 expression in each population were detected, respectively. A dual-luciferase reporter assay was developed to identify whether is a target gene of miR-7. After 10 Gy or sham irradiation of astrocytes, exosomes were extracted, stained with Dil (1,1'-Dioctadecyl-3,3,3',3'-Tetramethylindocarbocyanine Perchlorate), and added into non-irradiated astrocytes. Meanwhile, Dil-stained exosomes released from 10 Gy or sham irradiated astrocytes were injected into LC3B-GFP mice via the tail vein. Lung tissues were then extracted for western blotting and qRT-PCR. Irradiation of mouse brains increased the LC3B-II/I ratio, Beclin-1 and miR-7 levels, while decreased the Bcl-2 level in non-irradiated lung tissue. Interestingly, brain irradiation remarkably increased the miR-7 expression in astrocyte and oligodendrocyte. MiR-7 significantly inhibited the luciferase activity of the wild-type -3'-untranslated regions (UTR) reporter vector, but not that of the -3'-UTR mutant vector, indicating that is directly targeted by miR-7. In study, the addition of irradiated astrocyte-secreted exosomes increased the LC3B-II/I ratio, Beclin-1 and miR-7 levels, while decreased the Bcl-2 level in non-irradiated astrocytes. Further, the injection of irradiated astrocyte-secreted exosomes through the tail vein increased the lung LC3B-II/I ratio, Beclin-1 and miR-7 level, but decreased the Bcl-2 level . We concluded that exosomal miR-7 targets to mediate distant bystander autophagy in the lungs after brain irradiation.
本研究旨在探讨脑照射后,小鼠肺部旁观者自噬是否受外泌体 microRNA-7(miR-7)介导。对小鼠脑部进行 10 Gy 或假照射后,提取肺组织,通过免疫组织化学、Western blot 和实时定量逆转录 PCR(qRT-PCR)检测自噬标志物,同时分离大脑中的神经元/星形胶质细胞/小胶质细胞/少突胶质细胞,分别检测各群体中的 miR-7 表达。通过双荧光素酶报告基因检测鉴定是否为 miR-7 的靶基因。对星形胶质细胞进行 10 Gy 或假照射后,提取外泌体,用 Dil(1,1'-二辛基-3,3,3',3'-四甲基吲哚碳花青高氯酸盐)染色,加入未照射的星形胶质细胞。同时,将来自 10 Gy 或假照射星形胶质细胞的 Dil 染色外泌体通过尾静脉注入 LC3B-GFP 小鼠。然后提取肺组织进行 Western blot 和 qRT-PCR。脑照射增加了非照射肺组织中的 LC3B-II/I 比值、Beclin-1 和 miR-7 水平,同时降低了 Bcl-2 水平。有趣的是,脑照射显著增加了星形胶质细胞和少突胶质细胞中的 miR-7 表达。miR-7 显著抑制野生型-3'UTR 报告载体的荧光素酶活性,但不抑制-3'UTR 突变载体的荧光素酶活性,表明直接靶向 miR-7。在本研究中,添加辐照星形胶质细胞分泌的外泌体增加了非照射星形胶质细胞中的 LC3B-II/I 比值、Beclin-1 和 miR-7 水平,同时降低了 Bcl-2 水平。此外,通过尾静脉注射辐照星形胶质细胞分泌的外泌体增加了肺 LC3B-II/I 比值、Beclin-1 和 miR-7 水平,但降低了 Bcl-2 水平。我们得出结论,外泌体 miR-7 通过靶向来介导脑照射后肺部的远距离旁观者自噬。