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MiRNA Expression Profile of the Myocardial Tissue of Pigs with Coronary Microembolization

机译:冠状动脉微栓塞术猪心肌组织的miRNA表达谱

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>Background/Aims: Coronary microembolization (CME) is a serious complication of coronary heart disease and is considered as a strong predictor of poor long-term prognosis and major cardiac adverse events. Here, we identified differentially expressed microRNAs (miRNAs) in the myocardial tissue of CME pigs, and predicted and analyzed the possible functions of their target genes. Methods: Twelve Bama mini-pigs were randomly assigned to the sham and CME group (n = 6 in each group). The two groups were compared with regard to heart function, area of infarction, cardiomyocyte apoptosis, and myocardial expression of TNF-?±, IL-1?2 and IL-6. Further, miRNA chip analysis was used to screen for differentially expressed miRNAs, and the results were validated by real-time PCR. Bioinformatics methods were used to predict and analyze the functions of the target genes of the identified miRNAs. Results: The model CME pigs showed significantly increased expression of TNF-?±, IL-1?2 and IL-6, as well as micro-infarction lesions and cell apoptosis in the myocardial tissue. Thus, the model was established successfully. In the myocardial tissue of the CME pigs, the expression of ssc-miR-92b-5p, ssc-miR-491, ssc-miR-874, ssc-miR-425-3p, ssc-miR-376a-5p, ssc-miR-370, ssc-miR-30c-3p, ssc-miR-493-5p and ssc-miR-323 was significantly increased, whereas the expression of ssc-miR-136 and ssc-miR-142-3p was significantly decreased. GO and KEGG pathway analysis indicated that the target genes of these miRNAs are mainly associated with cell proliferation, apoptosis, necrosis, inflammation, and fibrosis. Conclusion: The differentially expressed miRNAs identified in the myocardial tissue of CME pigs could be new biomarkers or potential treatment targets for CME.
机译:> 背景/目标: 冠状动脉微栓塞术(CME)是冠心病的严重并发症,被认为是长期预后不良和严重心脏疾病的有力预测指标不良事件。在这里,我们确定了CME猪心肌组织中差异表达的microRNA(miRNA),并预测和分析了其靶基因的可能功能。 方法: 将12只巴马小型猪随机分配至假手术和CME组(每组n = 6)。比较两组的心功能,梗塞面积,心肌细胞凋亡以及TNF-α,IL-1β2和IL-6的心肌表达。此外,使用miRNA芯片分析筛选差异表达的miRNA,并通过实时PCR验证了结果。生物信息学方法用于预测和分析已鉴定的miRNA的靶基因的功能。 结果: CME模型猪显示TNF-α±,IL-1β2和IL-6的表达显着增加,以及微梗塞病变和细胞凋亡在心肌组织中。这样就成功建立了模型。在CME猪的心肌组织中,ssc-miR-92b-5p,ssc-miR-491,ssc-miR-874,ssc-miR-425-3p,ssc-miR-376a-5p,ssc- miR-370,ssc-miR-30c-3p,ssc-miR-493-5p和ssc-miR-323显着增加,而ssc-miR-136和ssc-miR-142-3p的表达则明显减少。 GO和KEGG通路分析表明,这些miRNA的靶基因主要与细胞增殖,凋亡,坏死,炎症和纤维化有关。 结论: 在CME猪的心肌组织中鉴定到的差异表达的miRNAs可能是CME的新生物标记或潜在治疗靶标。

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