Physiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.
Cancer Research UK Cambridge Institute, Cambridge CB2 0RE, UK.
Cell Metab. 2018 Apr 3;27(4):898-913.e7. doi: 10.1016/j.cmet.2018.02.020.
Animals require an immediate response to oxygen availability to allow rapid shifts between oxidative and glycolytic metabolism. These metabolic shifts are highly regulated by the HIF transcription factor. The factor inhibiting HIF (FIH) is an asparaginyl hydroxylase that controls HIF transcriptional activity in an oxygen-dependent manner. We show here that FIH loss increases oxidative metabolism, while also increasing glycolytic capacity, and that this gives rise to an increase in oxygen consumption. We further show that the loss of FIH acts to accelerate the cellular metabolic response to hypoxia. Skeletal muscle expresses 50-fold higher levels of FIH than other tissues: we analyzed skeletal muscle FIH mutants and found a decreased metabolic efficiency, correlated with an increased oxidative rate and an increased rate of hypoxic response. We find that FIH, through its regulation of oxidation, acts in concert with the PHD/vHL pathway to accelerate HIF-mediated metabolic responses to hypoxia.
动物需要对氧气供应做出即时反应,以允许氧化和糖酵解代谢之间快速转换。这些代谢转换由 HIF 转录因子高度调控。HIF 抑制因子(FIH)是一种天冬酰胺羟化酶,以氧依赖性方式控制 HIF 转录活性。我们在这里表明,FIH 的缺失会增加氧化代谢,同时也会增加糖酵解能力,从而导致耗氧量增加。我们进一步表明,FIH 的缺失会加速细胞对缺氧的代谢反应。骨骼肌中 FIH 的表达水平比其他组织高 50 倍:我们分析了骨骼肌 FIH 突变体,发现代谢效率降低,与氧化速率增加和缺氧反应速率增加相关。我们发现,FIH 通过其对氧化的调节,与 PHD/vHL 途径协同作用,加速 HIF 介导的缺氧代谢反应。