Rider Mark H
de Duve Institute and Université Catholique de Louvain, Avenue Hippocrate 75, 1200, Brussels, Belgium.
J Comp Physiol B. 2016 Jan;186(1):1-16. doi: 10.1007/s00360-015-0920-x. Epub 2015 Jul 15.
AMP-activated protein kinase (AMPK) is a highly conserved eukaryotic protein serine/threonine kinase that controls cellular and whole body energy homoeostasis. AMPK is activated during energy stress by a rise in AMP:ATP ratio and maintains energy balance by phosphorylating targets to switch on catabolic ATP-generating pathways, while at the same time switching off anabolic ATP-consuming processes. Metabolic depression is a strategy used by many animals to survive environmental stress and has been extensively studied across phylogeny by comparative biochemists and physiologists, but the role of AMPK has only recently been addressed. This review first deals with the evolution of AMPK in eukaryotes (excluding plants and fungi) and its regulation. Changes in adenine nucleotides and AMPK activation are described in animals during environmental energy stress, before considering the involvement of AMPK in controlling β-oxidation, fatty acid synthesis, triacylglycerol mobilization and protein synthesis. Lastly, strategies are presented to validate the role of AMPK in mediating metabolic depression by phosphorylating downstream targets.
AMP激活的蛋白激酶(AMPK)是一种高度保守的真核蛋白丝氨酸/苏氨酸激酶,可控制细胞和全身的能量稳态。在能量应激期间,AMPK通过AMP:ATP比值的升高而被激活,并通过磷酸化靶标来维持能量平衡,从而开启分解代谢产生ATP的途径,同时关闭合成代谢消耗ATP的过程。代谢抑制是许多动物用来应对环境压力的一种策略,比较生物化学家和生理学家已经在系统发育过程中对其进行了广泛研究,但AMPK的作用直到最近才得到关注。本文首先探讨了AMPK在真核生物(不包括植物和真菌)中的进化及其调控。在考虑AMPK参与控制β-氧化、脂肪酸合成、三酰甘油动员和蛋白质合成之前,先描述了动物在环境能量应激期间腺嘌呤核苷酸的变化和AMPK的激活情况。最后,提出了一些策略,以验证AMPK通过磷酸化下游靶标介导代谢抑制的作用。