Department of Radiation and Medical Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, Zhejiang, China.
Department of Orthopedics, The First Affiliated Hospital, Wenzhou Medical University, Wenzhou 325000, Zhejiang, China.
Aging (Albany NY). 2020 Dec 3;13(1):1357-1368. doi: 10.18632/aging.202319.
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 . This makes miR-18a a potentially useful target for the treatment of diabetes mellitus in the future.
miR-17-92 簇(miR-17、miR-18a、miR-19a、miR-20a、miR-19b-1 和 miR-92a)通过抑制多个靶基因参与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 型糖尿病患者血清 miR-18a 水平低于健康对照组,提示 miR-18a 可能影响血糖水平。在转基因小鼠中全局过表达 miR-18a 可提高其葡萄糖耐量和胰岛素敏感性,同时降低其骨骼肌和脂肪组织中磷酸酶和张力蛋白同源物缺失的基因(PTEN)的表达。Western blot 表明,在 3T3-L1 和 C2C12 细胞中过表达 miR-18a 可增强胰岛素刺激的 AKT 磷酸化并抑制 PTEN 表达,而抑制 miR-18a 则产生相反的效果。这些结果表明,miR-18a 通过下调. 这使得 miR-18a 成为未来治疗糖尿病的潜在有用靶点。