通过WARS对胰岛素受体的ptophanylation减弱了胰岛素信号传递
Wen-Xing Sun1,2, Kai-Hui Zhang1,3,4, Qian Zhou1,5
1Obstetrics and Gynecology Hospital of Fudan University, Institutes of Biomedical Sciences, Institute of Metabolism and Integrative Biology, Fudan University, Shanghai, People's Republic of China.
Cellular and molecular life sciences : CMLS
|January 11, 2024
概括
高水平的托芬会通过修改胰岛素受体引起胰岛素抵抗. 这一发现为治疗2型糖尿病 (T2D) 和相关代谢障碍提供了潜在的新点.
科学领域:
- 生物化学 生物化学
- 代谢疾病 代谢疾病
- 分子生物学分子生物学
背景情况:
- 氨基酸水平升高与胰岛素抵抗和2型糖尿病 (T2D) 有关.
- 连接氨基酸与胰岛素信号受损的精确分子机制尚未完全理解.
研究的目的:
- 阐明托芬影响胰岛素信号和葡萄糖吸收的机制.
- 为了确定缓解托诱导的胰岛素耐药性的分子标.
主要方法:
- 研究了富含托芬的饮食对小鼠胰岛素耐药性的影响.
- 利用生物化学测试来分析胰岛素受体 (IR) 和下游信号通路的修改.
- 研究了三甲基-tRNA合成酶 (WARS) 和SIRT1在调节IR修饰和胰岛素敏感性的作用.
主要成果:
- 被食富含托芬的小鼠表现出胰岛素抵抗.
- 托芬在IR上促进了WARS介导的 lysine 1209的托法尼化 (IRW-K1209).
- IRW-K1209 抑制了胰岛素刺激的IR,AKT和AS160的酸化,损害了葡萄糖的吸收. SIRT1可以逆转这种变化,增强胰岛素敏感性.
结论:
- 托芬通过WARS.直接通过修改胰岛素受体来损害胰岛素信号传递.
- SIRT1在逆转托对胰岛素敏感性的影响方面发挥着至关重要的作用.
- WARS成为减弱T2D胰岛素抵抗的潜在治疗标.
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