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miR-186-5p Promotes Apoptosis by Targeting IGF-1 in SH-SY5Y OGD/R Model

机译:miR-186-5p通过在SH-SY5Y OGD / R模型中靶向IGF-1促进细胞凋亡

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摘要

In recent years, accumulating evidence has revealed that microRNAs play critical roles in ischemia stroke. This study was designed to investigate the expression level and effects of microRNA (miR)-186-5p on ischemia stroke, and its underlying molecular mechanism. Firstly, we demonstrated that miR-186-5p were significantly up-regulated and induced apoptosis in oxygen and glucose deprivation/reperfusion (OGD/R) model. Moreover, we found that miR-186-5p reduced the expression of insulin-like growth factor (IGF)-1, an essential factor for the development of the nervous system. Meanwhile, miR-186-5p inhibitor enhanced cell viability and IGF-1 expression. Furthermore, IGF-1 was confirmed as a direct target gene of miR-186-5p by luciferase activity assay. In addition, miR-186-5p was upregulated in ischemia stroke patients' serum compared with healthy donors. These data demonstrated that miR-186-5p was an adverse factor by inducing neuron apoptosis and suppressing IGF-1 in ischemia stroke model, and suggested that miR-186-5p may be a diagnostic marker and potential therapeutic target for ischemia stroke patients.
机译:近年来,越来越多的证据表明,microRNA在缺血性中风中起关键作用。本研究旨在研究microRNA(miR)-186-5p在缺血性中风中的表达水平及其作用,及其潜在的分子机制。首先,我们证明了在氧气和葡萄糖剥夺/再灌注(OGD / R)模型中,miR-186-5p显着上调并诱导了细胞凋亡。此外,我们发现miR-186-5p减少了胰岛素样生长因子(IGF)-1的表达,而胰岛素样生长因子(IGF)-1是神经系统发育的重要因素。同时,miR-186-5p抑制剂可增强细胞活力和IGF-1表达。此外,通过荧光素酶活性测定,IGF-1被证实是miR-186-5p的直接靶基因。此外,与健康供体相比,缺血性卒中患者血清中的miR-186-5p上调。这些数据表明,miR-186-5p是诱导缺血性中风模型中神经元凋亡和抑制IGF-1的不利因素,并暗示miR-186-5p可能是缺血性中风患者的诊断标志物和潜在治疗靶标。

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