安普克
合成代谢
磷酸化
分解代谢
细胞生物学
胞浆
调节器
AMP活化蛋白激酶
化学
线粒体
营养物
生物
蛋白激酶A
新陈代谢
生物化学
生态学
酶
基因
作者
Yue Zong,Chen‐Song Zhang,Mengqi Li,Wen Wang,Zhichao Wang,Simon A. Hawley,Teng Ma,Jin-Wei Feng,Xiao Tian,Qi Qu,Yuqing Wu,Cixiong Zhang,Zhiyun Ye,Shu‐Yong Lin,Hai‐long Piao,D. Grahame Hardie,Sheng‐Cai Lin
出处
期刊:Cell Research
[Springer Nature]
日期:2019-04-04
卷期号:29 (6): 460-473
被引量:114
标识
DOI:10.1038/s41422-019-0163-6
摘要
AMPK, a master regulator of metabolic homeostasis, is activated by both AMP-dependent and AMP-independent mechanisms. The conditions under which these different mechanisms operate, and their biological implications are unclear. Here, we show that, depending on the degree of elevation of cellular AMP, distinct compartmentalized pools of AMPK are activated, phosphorylating different sets of targets. Low glucose activates AMPK exclusively through the AMP-independent, AXIN-based pathway in lysosomes to phosphorylate targets such as ACC1 and SREBP1c, exerting early anti-anabolic and pro-catabolic roles. Moderate increases in AMP expand this to activate cytosolic AMPK also in an AXIN-dependent manner. In contrast, high concentrations of AMP, arising from severe nutrient stress, activate all pools of AMPK independently of AXIN. Surprisingly, mitochondrion-localized AMPK is activated to phosphorylate ACC2 and mitochondrial fission factor (MFF) only during severe nutrient stress. Our findings reveal a spatiotemporal basis for hierarchical activation of different pools of AMPK during differing degrees of stress severity.
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