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Increased expression of microRNA-378a-5p in acute ethanol exposure of rat cardiomyocytes

机译:大鼠心肌细胞急性乙醇暴露中microRNA-378a-5p表达的增加

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Alcohol abuse is a risk factor for a distinct form of congestive heart failure, known as alcoholic cardiomyopathy (ACM). Here, we investigate how microRNAs may participate in the induction of cardiomyocyte apoptosis associated with ethanol exposure in vitro. Increasing the concentrations of ethanol to primary rat cardiomyocytes resulted in elevated apoptosis assessed by annexin V and propidium iodide staining, and reduced expression of an enzyme for alcohol detoxification aldehyde dehydrogenase 2 (ALDH2). These ethanol effects were accompanied by a substantial elevation of miR-378a-5p. Driving miR-378a-5p overexpression in cardiomyocytes decreased ALDH2. The specific interaction of miR-378a-5p with the 3’UTR of ALDH2 was examined by luciferase reporter assays, and we found that miR-378a-5p activity depends on a complementary base pairing at the 3′-UTR region of ALDH2 mRNA. Finally, ethanol-induced apoptosis in cardiomyocytes was attenuated in the presence of anti-miR378a-5p. Collectively, these data implicate a likely involvement of miR-378a-5p in the stimulation of cardiomyocyte apoptosis through ALDH2 gene suppression, which might play a potential role in the pathogenesis of ACM.
机译:酗酒是导致充血性心力衰竭独特形式的危险因素,称为酒精性心肌病(ACM)。在这里,我们调查microRNA如何参与与乙醇暴露相关的心肌细胞凋亡的诱导。增加乙醇对原代大鼠心肌细胞的浓度导致膜联蛋白V和碘化丙啶染色评估细胞凋亡增加,并降低了酒精解毒醛脱氢酶2(ALDH2)的酶表达。这些乙醇作用伴随着miR-378a-5p的显着升高。驱动心肌细胞中的miR-378a-5p过表达降低了ALDH2。通过荧光素酶报告基因分析检测了miR-378a-5p与ALDH2 3'UTR的特异性相互作用,我们发现miR-378a-5p的活性取决于ALDH2 mRNA 3'-UTR区的互补碱基配对。最后,在抗miR378a-5p存在下,乙醇诱导的心肌细胞凋亡得以减弱。总的来说,这些数据暗示miR-378a-5p可能通过ALDH2基因抑制刺激心肌细胞凋亡,这可能在ACM的发病机制中发挥潜在作用。

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