祖靓, 朱荣. 2013: 力竭运动对小鼠骨骼肌细胞自噬的影响及相关调节机制研究. 体育科学, 33(9): 77-84. DOI: 10.16469/j.css.2013.09.004
    引用本文: 祖靓, 朱荣. 2013: 力竭运动对小鼠骨骼肌细胞自噬的影响及相关调节机制研究. 体育科学, 33(9): 77-84. DOI: 10.16469/j.css.2013.09.004
    ZU Jing, ZHU Rong. 2013: Effects of Exhaustive Exercise on Autophagy and Relevant Regulatory Mechanisms in Murine Skeletal Muscle Cell. China Sport Science, 33(9): 77-84. DOI: 10.16469/j.css.2013.09.004
    Citation: ZU Jing, ZHU Rong. 2013: Effects of Exhaustive Exercise on Autophagy and Relevant Regulatory Mechanisms in Murine Skeletal Muscle Cell. China Sport Science, 33(9): 77-84. DOI: 10.16469/j.css.2013.09.004

    力竭运动对小鼠骨骼肌细胞自噬的影响及相关调节机制研究

    Effects of Exhaustive Exercise on Autophagy and Relevant Regulatory Mechanisms in Murine Skeletal Muscle Cell

    • 摘要: 目的:研究力竭运动对C57BL/6小鼠骨骼肌细胞自噬的影响, 并探讨AMPK在骨骼肌自噬中的作用和调节机制。方法:8周龄C57BL/6小鼠96只, 随机分为AICAR注射组, 力竭运动组, Compound C注射+力竭运动组及相应对照组。各组小鼠分别在AICAR注射后1h, 2h和6h或在进行终强度为11m/min的力竭跑台运动后即刻, 3h, 6h, 12h, 24h取材, 每组6只。通过ELISA法测定AMPK酶活性, 采用Western Blot法测定p-ULK1, ATG 7, LC3, Beclin1和p62蛋白表达, 免疫共沉淀法测定AMPK/ULK1结合量。结果:AICAR注射后1h时AMPK酶活性、p-ULK1、AMPK/ULK1结合量、LC3-I和LC3-II显著升高 (P<0.05) , LC3-II/LC3-I比值显著增大 (P<0.01) , ATG 7、Beclin1显著下降 (P<0.05) , p62变化不明显, 2h时除LC3-II显著下降外 (P<0.01) , 其余指标基本恢复;力竭运动组AMPK酶活性, p-ULK1、AMPK/ULK1结合量, LC3-I和LC3-II运动结束即刻增加非常显著 (P<0.01) , LC3-II/LC3-I比值显著增大 (P<0.01) , 恢复期 (3h、6h、12h、24h) 显著下降 (P<0.01) , ATG 7、Beclin1和p62运动后即刻显著下降 (P<0.05) , 恢复期ATG 7始终低于对照组, Beclin1和p62逐渐恢复;Compound C注射+力竭运动组AMPK活性, p-ULK1含量和AMPK/ULK1结合量基本不变, LC3-I, LC3-II和LC3-II/LC3-I比值在运动后变化同力竭组一致, 但显著低于力竭组 (P<0.05) , ATG 7, Beclin1变化同力竭组, 但显著高于力竭组 (P<0.05) , p62在运动后即刻显著升高, 恢复期 (3h、6h、12h、24h) 显著下降 (P<0.05) 。结论:AMPK是骨骼肌内细胞自噬的重要调节因子, 力竭运动可以通过AMPK/ULK1途径显著提高骨骼肌细胞自噬水平, 但AMPK/ULK1并非是调节骨骼肌细胞自噬的唯一途径。

       

      Abstract: Objective:The effects of exhaustive exercise on autophagy in skeletal muscles of C57BL/6mice were studied to explore the role and mechanism of AMPK in autophagy regulation.Methods:96 eight-week C57BL6 mice were randomly divided into AICAR injection group, exhaustive exercise group, compound C injection+exhaustive exercise group and corresponding control groups.Mice were killed at 1h, 2hand 6hrespectively after AICAR injection or sacrificed at immediately after exhaustive exercise, 3h, 6h, 12hand 24hrespectively after running to exhaustion at a final speed of 11m/min.ELISA was used to analyze AMPK activity, Western blot analysis was used to test protein expression of p-ULK1, ATG7, LC3, Beclin1 and p62while the interaction of AMPK and ULK1was measured by co-immunoprecipitation.Results:Compared to SC group, AMPK activity, p-ULK1, the interaction between AMPK and ULK1, LC3-I, LC3-II as well as the ration of LC3-II/LC3-I increased markedly 1hafter AICAR injection while Beclin1, ATG7decreased significantly (P<0.05) and p62remained unchanged.All return to normal after 2h besides LC3-II decreased continuously.For EE groups, AMPK activity, p-ULK1, AMPK/ULK1interaction, LC3-I, LC3-II and ratio of LC3II/LC3-I increased significantly immediately after exercise (P<0.01) and decreased significantly at recovery period (3h, 6h, 12h, 24h) (P<0.05) .Beclin1, ATG7and p62decreased significantly immediately after exercise while ATG7remained lower than SC group, Beclin1and p62gradually recovered.However, exhaustive exercise did not influence AMPK activity, pULK1and the interaction of AMPK/ULK1after Compound C injection.LC3-I, LC3-II and ratio of LC3-II/LC3-I changed similar to EE group but they are greatly lower than EE group (P<0.05) .Atg7, Beclin1changed similar to EE group, but they are still higher than EE (P <0.05) .p62increased significantly immediately after exercise and dropped at recovery period (3h, 6h, 12h, 24h) (P<0.05) .Conclusion:AMPK plays a great role in autophagy regulation in murine skeletal muscle.Exhaustive exercise significantly activates autophagy of skeletal muscle via AMPK/ULK1pathway, but AMPK is not the only pathway involved in this process.

       

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