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miR-18a increases insulin sensitivity by inhibiting

机译:miR-18a通过抑制增加胰岛素敏感性

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摘要

The miR-17-92 cluster (miR-17, miR-18a, miR-19a, miR-20a, miR-19b-1 and miR-92a) contributes to the occurrence and development of various diseases by inhibiting multiple target genes. Here, we explored the effects of miR-18a on insulin sensitivity. Quantitative real-time PCR indicated that serum miR-18a levels were lower in type 2 diabetes mellitus patients than in healthy controls, suggesting that miR-18a may influence blood glucose levels. Global overexpression of miR-18a in transgenic mice increased their glucose tolerance and insulin sensitivity, while it reduced expression of the phosphatase and tensin homolog deleted on chromosome ten (PTEN) in their skeletal muscle and adipose tissue. Western blotting indicated that overexpressing miR-18a in 3T3-L1 and C2C12 cells enhanced insulin-stimulated AKT phosphorylation and suppressed PTEN expression, while inhibiting miR-18a had the opposite effects. These results suggest that miR-18a improves insulin sensitivity by downregulating PTEN. This makes miR-18a a potentially useful target for the treatment of diabetes mellitus in the future.
机译:MiR-17-92簇(miR-17,miR-18a,miR-19a,miR-20a,miR-19b-1和mir-92a)通过抑制多种靶基因来促进各种疾病的发生和发展。在这里,我们探讨了miR-18a对胰岛素敏感性的影响。定量实时PCR表明,2型糖尿病患者的血清miR-18a水平均低于健康对照,表明miR-18a可能影响血糖水平。在转基因小鼠中MiR-18a的全局过表达增加了它们的葡萄糖耐量和胰岛素敏感性,而在其骨骼肌和脂肪组织中,它降低了磷酸酶和染色体上的染色体10(PTEN)的表达。 Western印迹表明,过表达MiR-18a在3T3-L1和C2C12细胞中增强了胰岛素刺激的AKT磷酸化和抑制的PTEN表达,同时抑制miR-18a具有相反的效果。这些结果表明miR-18a通过下调PTEN来提高胰岛素敏感性。这使得miR-18a在未来治疗糖尿病的潜在有用的目标。

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