State Key Laboratory for Cellular Stress Biology, School of Life Sciences, Xiamen University, 361102, Fujian, China.
CAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 116023, Dalian, China.
Cell Res. 2019 Jun;29(6):460-473. doi: 10.1038/s41422-019-0163-6. Epub 2019 Apr 4.
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.
AMPK,代谢稳态的主控器,可被 AMP 依赖和 AMP 非依赖的机制激活。这些不同机制运作的条件及其生物学意义尚不清楚。在这里,我们表明,根据细胞 AMP 升高的程度,不同的 AMPK 区室化池被激活,磷酸化不同的靶标。低糖通过溶酶体中的 AMP 非依赖、AXIN 为基础的途径,仅激活 AMPK,以磷酸化 ACC1 和 SREBP1c 等靶标,发挥早期抗合成代谢和促分解代谢的作用。中等程度的 AMP 增加也以 AXIN 依赖的方式扩展到激活胞质 AMPK。相比之下,高浓度的 AMP,来自严重的营养胁迫,独立于 AXIN 激活所有 AMPK 池。令人惊讶的是,线粒体定位的 AMPK 仅在严重的营养胁迫下被激活,以磷酸化 ACC2 和线粒体分裂因子(MFF)。我们的发现揭示了在不同程度的应激严重程度下,不同 AMPK 池的分层激活的时空基础。