Section for Physiology and Cell Biology, Department of Biosciences, University of Oslo, Oslo, Norway.
Am J Physiol Regul Integr Comp Physiol. 2024 Feb 1;326(2):R184-R195. doi: 10.1152/ajpregu.00211.2023. Epub 2023 Dec 25.
The hypoxia-inducible factor (HIF) is considered key in the transcriptional response to low oxygen. Yet, the role of HIF in the absence of oxygen (anoxia) and in preparation for reoxygenation remains unclear. Recent studies suggest that mounting a HIF response may be counterproductive for anoxia survival. We here studied one of the champions of anoxia survival, the crucian carp (), and hypothesized that expression of prolyl hydroxylase domains (PHDs; the upstream regulators of HIF) are upregulated to circumvent an energy-costly activation of HIF in anoxia and to prepare for reoxygenation. We measured whole brain mRNA and protein levels of the three isoforms PHD1, PHD2, and PHD3, coded for by multiple paralogs of the genes , , and , using quantitative PCR and Western blotting in the brain of crucian carps exposed to 5 days normoxia or anoxia, and 5 days anoxia followed by 3 or 24 h of reoxygenation. The mRNA levels of most paralogs were increased in anoxia and upon reoxygenation, with showing the largest increase in mRNA level (up to 17-fold) and highest relative mRNA abundance (up to 75% of expressed ). The protein level of all PHDs was maintained in anoxia and increased upon reoxygenation. We then explored PHD distribution in different brain regions and found PHD immunoreactivity to be associated with axonal branches and showing region-specific changes during anoxia-reoxygenation. Our results support an overall upregulation of under prolonged anoxia and PHDs upon reoxygenation in crucian carp, likely aimed at suppressing HIF responses, although regional differences are apparent in such a complex organ as the brain. We report a profound upregulation of most paralog mRNA levels in anoxia and upon reoxygenation, with showing the largest, a 17-fold increase, and highest relative mRNA abundance. The relative abundance of prolyl hydroxylase domain (PHD) proteins was maintained during anoxia and increased at reoxygenation. PHD immunoreactivity was localized to axonal branches with region-specific changes during anoxia-reoxygenation. These dynamic and regional changes in crucian carp, champion of anoxia tolerance, are most likely adaptive and call for further mechanistic studies.
缺氧诱导因子 (HIF) 被认为是对低氧反应的关键。然而,HIF 在缺氧(缺氧)和再氧合准备中的作用仍不清楚。最近的研究表明,引发 HIF 反应可能不利于缺氧生存。在这里,我们研究了缺氧生存的冠军之一——鲫鱼(),并假设脯氨酰羟化酶结构域(PHD;HIF 的上游调节剂)的表达上调,以避免缺氧时能量消耗的 HIF 激活,并为再氧合做准备。我们使用定量 PCR 和 Western blot 在暴露于 5 天常氧或缺氧以及 5 天缺氧后 3 或 24 小时再氧合的鲫鱼大脑中测量了编码基因的三个同工型 PHD1、PHD2 和 PHD3 的多个基因的 prolyl 羟化酶结构域 (PHD) 的全长脑 mRNA 和蛋白水平。在缺氧和再氧合时,大多数基因的 mRNA 水平增加,其中基因的 mRNA 水平增加最大(高达 17 倍),相对 mRNA 丰度最高(高达表达的 75%)。在缺氧时所有 PHD 的蛋白水平保持不变,再氧合时增加。然后,我们探索了 PHD 在不同脑区的分布,发现 PHD 免疫反应与轴突分支有关,并在缺氧-再氧合过程中表现出区域特异性变化。我们的结果支持鲫鱼在长时间缺氧和再氧合时总体上调,并且可能旨在抑制 HIF 反应,尽管在大脑等复杂器官中存在区域差异。我们报告了在缺氧和再氧合时大多数基因的 mRNA 水平显著上调,其中基因的 mRNA 水平上调最大,增加了 17 倍,相对 mRNA 丰度最高。在缺氧时,PHD 蛋白的相对丰度保持不变,再氧合时增加。PHD 免疫反应定位于轴突分支,在缺氧-再氧合过程中具有区域特异性变化。这些在鲫鱼中动态和区域变化,缺氧耐受的冠军,很可能是适应性的,并呼吁进一步的机制研究。