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CircHIPK3 regulates the autophagy and apoptosis of hypoxia/reoxygenation-stimulated cardiomyocytes via the miR-20b-5p/ATG7 axis

机译:Circhipk3通过MiR-20B-5P / ATG7轴来调节缺氧/雷诺化刺激的心肌细胞的自噬和凋亡

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摘要

A Mice were subjected to 60 min of ischemia and 3 h of reperfusion. Representative transmission electron microscopy (TEM) images of hearts show the presence of autophagosomes (red arrow). Scale bar = 1 μm. B RT-qPCR analysis of circHIPK3 expression in mouse heart samples undergoing I/R or sham treatment. n = 3. C LC3-II and P62 expression were analyzed by western blotting in H/R (6 h hypoxia followed by 4 h reoxygenation)-stimulated cardiomyocytes. n = 3. D Increased expression of circHIPK3 in H/R-stimulated cardiomyocytes. n = 9. E Cardiomyocytes were transfected with negative control (LV), circHIPK3 overexpression vector, or circHIPK3 siRNA (si-circHIPK3) for 48 h. F Representative electron microscope analysis of autophagosomes in cardiomyocytes. Scale bar = 2 μm. G LC3-II and Beclin 1 expression were analyzed by western blotting in cardiomyocytes. *P < 0.05 compared with the sham or normal group. #P < 0.05 compared with the H/R group.
机译:对小鼠进行60分钟的缺血和3小时再灌注。心脏的代表性透射电子显微镜(TEM)图像显示自噬体(红色箭头)的存在。秤杆=1μm。 B RT-QPCR分析I / R或假处理的小鼠心脏样品中Circhipk3表达的分析。 N = 3. C LC3-II和P62表达通过Western印迹分析H / R(6小时缺氧,然后是4h Reoxygenation) - 刺激的心肌细胞。 n = 3. D增加了H / R刺激心肌细胞的Circhipk3的表达。 n = 9. e心肌细胞用阴性对照(LV),CirchipK3过表达载体或Circhipk3 siRNA(Si-Circhipk3)转染48小时。 F类心肌细胞自噬复印件的代表性电子显微镜分析。秤杆=2μm。通过在心肌细胞中蛋白质印迹分析G LC3-II和BECLIN1表达。 * P <0.05与假或正常组相比。 #p <0.05与H / R组相比。

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