| Literature DB >> 30948787 |
Yue Zong1, Chen-Song Zhang1, Mengqi Li1, Wen Wang2,3, Zhichao Wang2,3, Simon A Hawley4, Teng Ma1, Jin-Wei Feng1, Xiao Tian1, Qu Qi1, Yu-Qing Wu1, Cixiong Zhang1, Zhiyun Ye1, Shu-Yong Lin1, Hai-Long Piao2,3, D Grahame Hardie4, Sheng-Cai Lin5.
Abstract
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.Entities:
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Year: 2019 PMID: 30948787 PMCID: PMC6796943 DOI: 10.1038/s41422-019-0163-6
Source DB: PubMed Journal: Cell Res ISSN: 1001-0602 Impact factor: 25.617