Institute of Veterinary Physiology, University of Leipzig, D-04103 Leipzig, Germany.
Int J Mol Sci. 2020 Mar 31;21(7):2428. doi: 10.3390/ijms21072428.
AMP-activated protein kinase (AMPK) is known as a pivotal cellular energy sensor, mediating the adaptation to low energy levels by deactivating anabolic processes and activating catabolic processes in order to restore the cellular ATP supply when the cellular AMP/ATP ratio is increased. Besides this well-known role, it has also been shown to exert protective effects under hypoxia. While an insufficient supply with oxygen might easily deplete cellular energy levels, i.e., ATP concentration, manifold other mechanisms have been suggested and are heavily disputed regarding the activation of AMPK under hypoxia independently from cellular AMP concentrations. However, an activation of AMPK preceding energy depletion could induce a timely adaptation reaction preventing more serious damage. A connection between AMPK and the master regulator of hypoxic adaptation via gene transcription, hypoxia-inducible factor (HIF), has also been taken into account, orchestrating their concerted protective action. This review will summarize the current knowledge on mechanisms of AMPK activation under hypoxia and its interrelationship with HIF.
腺苷酸活化蛋白激酶 (AMPK) 作为细胞能量传感器,当细胞 AMP/ATP 比值升高时,通过抑制合成代谢和激活分解代谢来适应低能量水平,从而恢复细胞内的 ATP 供应。除了这个众所周知的作用,它在缺氧条件下也表现出保护作用。虽然氧气供应不足很容易耗尽细胞的能量水平,即 ATP 浓度,但对于缺氧条件下 AMPK 的激活,除了细胞 AMP 浓度之外,还有多种其他机制被提出并存在很大争议,这些机制与独立于细胞 AMP 浓度的缺氧诱导因子 (HIF) 有关。然而,在能量耗竭之前激活 AMPK 可以诱导及时的适应反应,防止更严重的损伤。AMPK 与缺氧适应的主调控因子通过基因转录的 HIF 之间也存在联系,协调它们的协同保护作用。这篇综述将总结目前关于缺氧条件下 AMPK 激活的机制及其与 HIF 的相互关系的知识。