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葡萄糖饥饿的C2C12肌管中自噬的诱导及细胞代谢变化

Induction of Autophagy and Changes in Cellular Metabolism in Glucose Starved C2C12 Myotubes.

作者信息

Nakai Naoya, Kitai Saki, Iida Noriko, Inoue Sachika, Nakata Ken, Murakami Taro, Higashida Kazuhiko

机构信息

Laboratory of Exercise Nutrition, Department of Nutrition, University of Shiga Prefecture.

Medicine for Sports and Performing Arts, Graduate School of Medicine, Osaka University.

出版信息

J Nutr Sci Vitaminol (Tokyo). 2020;66(1):41-47. doi: 10.3177/jnsv.66.41.

Abstract

Mouse myoblast C2C12 cells are commonly used as a model system for investigating the metabolic regulation of skeletal muscle. As it is therefore important to understand the metabolic features of C2C12 cells, we examined the effect of glucose starvation on autophagy in C2C12 myotubes. After culture of C2C12 myotubes with high (HG, 25.0 mM) or low (LG, 5.6 mM) glucose concentrations, the concentration of glucose in the LG group had decreased to 0 mM after 24 h of culture and was around 17 mM after 48 h of culture in the HG group. The concentration of lactate increased from 0 to approximately 9 mM at 24 h and then dropped slightly in the LG group, while it increased linearly to 21 mM in the HG group at 48 h. The phosphorylation of p70 S6 kinase, marker for the protein translation initiation was significantly lower and the ratio of LC3-II/LC3-I, marker for the induction of autophagy was significantly higher in the LG group. GLUT1 and hexokinase II expression were significantly higher in the LG group. Together, these changes in glucose and lactate concentrations in the culture media suggest that C2C12 myotubes depend on anaerobic glycolysis. Our findings also suggest that glucose depletion stimulates the expression of key molecules involved in glycolysis and that cellular autophagy is also activated in C2C12 myotubes.

摘要

小鼠成肌细胞C2C12常用于研究骨骼肌代谢调节的模型系统。因此,了解C2C12细胞的代谢特征很重要,我们研究了葡萄糖饥饿对C2C12肌管自噬的影响。在高(HG,25.0 mM)或低(LG,5.6 mM)葡萄糖浓度下培养C2C12肌管后,LG组葡萄糖浓度在培养24小时后降至0 mM,HG组在培养48小时后约为17 mM。LG组乳酸浓度在24小时时从0增加到约9 mM,然后略有下降,而HG组在48小时时线性增加到21 mM。LG组中蛋白质翻译起始标志物p70 S6激酶的磷酸化显著降低,自噬诱导标志物LC3-II/LC3-I的比率显著升高。LG组中GLUT1和己糖激酶II的表达显著更高。总之,培养基中葡萄糖和乳酸浓度的这些变化表明C2C肌管依赖无氧糖酵解。我们的研究结果还表明,葡萄糖耗竭刺激了参与糖酵解的关键分子的表达,并且C2C12肌管中的细胞自噬也被激活。

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