AKT2型
蛋白激酶B
AKT1型
代谢途径
磷酸化
细胞生物学
糖酵解
信号转导
葡萄糖摄取
PI3K/AKT/mTOR通路
生物
骨骼肌
生物化学
嘧啶代谢
化学
酶
胰岛素
内分泌学
嘌呤
作者
Genki Kawamura,Toshiya Kokaji,Kentaro Kawata,Yuka Sekine,Yutaka Suzuki,Tomoyoshi Soga,Yoshibumi Ueda,Mizuki Endo,Shinya Kuroda,Takeaki Ozawa
出处
期刊:Science Signaling
[American Association for the Advancement of Science (AAAS)]
日期:2023-02-21
卷期号:16 (773)
被引量:1
标识
DOI:10.1126/scisignal.abn0782
摘要
Insulin regulates various cellular metabolic processes by activating specific isoforms of the Akt family of kinases. Here, we elucidated metabolic pathways that are regulated in an Akt2-dependent manner. We constructed a transomics network by quantifying phosphorylated Akt substrates, metabolites, and transcripts in C2C12 skeletal muscle cells with acute, optogenetically induced activation of Akt2. We found that Akt2-specific activation predominantly affected Akt substrate phosphorylation and metabolite regulation rather than transcript regulation. The transomics network revealed that Akt2 regulated the lower glycolysis pathway and nucleotide metabolism and cooperated with Akt2-independent signaling to promote the rate-limiting steps in these processes, such as the first step of glycolysis, glucose uptake, and the activation of the pyrimidine metabolic enzyme CAD. Together, our findings reveal the mechanism of Akt2-dependent metabolic pathway regulation, paving the way for Akt2-targeting therapeutics in diabetes and metabolic disorders.
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