磷酸甘油酸变位酶
骨骼肌
蛋白激酶B
PI3K/AKT/mTOR通路
生物化学
二十碳五烯酸
生物
碳水化合物代谢
化学
细胞生物学
信号转导
糖酵解
新陈代谢
内分泌学
脂肪酸
多不饱和脂肪酸
作者
Chenchen Li,Haigang Cao,Yingchun Ren,Jinrui Jia,Gongshe Yang,Jianjun Jin,Xin’e Shi
标识
DOI:10.1016/j.ijbiomac.2024.131547
摘要
Eicosapentaenoic acid regulates glucose uptake in skeletal muscle and significantly affects whole-body energy metabolism. However, the underlying molecular mechanism remains unclear. Here we report that eicosapentaenoic acid activates phosphoglycerate mutase 2, which mediates the conversion of 2-phosphoglycerate into 3-phosphoglycerate. This enzyme plays a pivotal role in glycerol degradation, thereby facilitating the proliferation and differentiation of satellite cells in skeletal muscle. Interestingly, phosphoglycerate mutase 2 inhibits mitochondrial metabolism, promoting the formation of fast-type muscle fibers. Treatment with eicosapentaenoic acid and phosphoglycerate mutase 2 knockdown induced opposite transcriptomic changes, most of which were enriched in the PI3K-AKT signaling pathway. Phosphoglycerate mutase 2 activated the PI3K-AKT signaling pathway, which inhibited the phosphorylation of FOXO1, and, in turn, inhibited mitochondrial function and promoted the formation of fast-type muscle fibers. Our results suggest that eicosapentaenoic acid promotes skeletal muscle growth and regulates glucose metabolism by targeting phosphoglycerate mutase 2 and activating the PI3K/AKT signaling pathway.
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