基础医学与临床 ›› 2013, Vol. 33 ›› Issue (5): 562-566.

• 研究论文 • 上一篇    下一篇

MicroRNA-29抑制胰岛素刺激的大鼠L6细胞葡萄糖吸收

刘长征1,李静静2,焦涛1,何小东3,常永生4   

  1. 1. 中国医学科学院基础医学研究所
    2. 中国医学科学院北京协和医院基本外科
    3. 北京协和医院
    4. 中国医学科学院基础医学研究所 北京协和医学院基础学院
  • 收稿日期:2013-01-16 修回日期:2013-03-19 出版日期:2013-05-05 发布日期:2013-05-29
  • 通讯作者: 常永生 E-mail:changy@ibms.pumc.edu.cn
  • 基金资助:
    重塑FOXA2-miR-29反馈调控网络可能恢复糖尿病小鼠血糖的稳定调节

MicroRNA-29 suppresses glucose uptake stimulated by insulin in L6 myotube cells

  • Received:2013-01-16 Revised:2013-03-19 Online:2013-05-05 Published:2013-05-29
  • Contact: Yong-sheng CHANG E-mail:changy@ibms.pumc.edu.cn

摘要: 目的 研究microRNA-29(miR-29)在糖尿病模型大鼠 (GK)骨骼肌组织中的表达,并探讨其对大鼠骨骼肌细胞L6葡萄糖吸收的影响。方法 利用real-time PCR方法检测miR-29家族,miR-29a、miR-29b及miR-29c在GK大鼠骨骼肌组织中的表达特征。L6骨骼肌细胞诱导分化为肌管细胞,经葡萄糖与胰岛素处理后,利用real-time PCR与Northern blot分析miR-29家族的表达情况。选择腺病毒表达系统在L6分化的肌管细胞中过表达或抑制内源miR-29的功能,利用葡萄糖吸收实验检测胰岛素刺激的葡萄糖吸收情况。结果 miR-29a、miR-29b及miR-29c在GK大鼠骨骼肌组织中表达上调。L6分化的肌管细胞经葡萄糖与胰岛素处理,miR-29b和miR-29c的表达上调,而miR-29a表达无明显变化。在L6分化的肌管细胞中过表达miR-29可以明显抑制胰岛素刺激的葡萄糖吸收。结论 miR-29参与了GK大鼠骨骼肌细胞葡萄糖耐受及胰岛素抵抗的产生,抑制其表达可能是治疗II型糖尿病的一种新策略。

关键词: microRNA-29, II型糖尿病, 葡萄糖耐受, 胰岛素抵抗

Abstract: Objective To evaluate the expression profile of miR-29 family in the skeletal muscle of GK rats and to further probe the function of miR-29 family in glucose uptake in L6 cells induced by insulin. Methods The expression of miR-29 family was detected by using real-time PCR. miR-29 levels in L6 cells treated by glucose and insulin were measured by using real-time PCR and Northern Blot. Gain of- or loss of- function of miR-29 was achieved by a recombinant adenovirus system and the effect of miR-29 on insulin resistance was measured by insulin-induced glucose uptake assay. Results miR-29a, miR-29b, and miR-29c expression was upregulated in the skeletal muscle of GK rats and miR-29b and miR-29c expression levels were elevated in L6 cells treated by glucose and insulin. Moreover, enforced expression of miR-29 significantly suppressed insulin-induced glucose uptake in L6 cells and loss-of-function of miR-29 by using Ad-sp-miR-29 led to an increase of glucose uptake. Conclusion miR-29 family is involved in the glucose tolerance and insulin resistance of GK rats and targeting miR-29 maybe provide a novel strategy for Type II diabetes therapy.

Key words: microRNA-29, Type II diabetes, glucose tolerance, insulin resistance

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