Role of Hypoxia-Inducible Factor 1α in Adaptation to Hypoxia in the Pathogenesis of Novel Coronavirus Disease 2019

R. Y. Kalinin, I. Suchkov, Sergey N. Raitsev, V. Zvyagina, Eduard S. Bel'skikh
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Abstract

INTRODUCTION: A novel coronavirus (severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2)) emerged in December 2019 and rapidly spread over the world having provoked a pandemic of respiratory disease. This highly pathogenic virus can attack the lung tissue and derange gas exchange leading to acute respiratory distress syndrome and systemic hypoxia. Hypoxic conditions trigger activation of adaptation mechanisms including hypoxia-inducible factor-1á (HIF-1á) which is involved in the regulation of the key processes, e. g, proliferation and metabolism of cells and angiogenesis. Besides, the level of HIF-1á expression is associated with the intensity of the immune response of an organism including that of the innate immunity mediating inflammatory reaction. Therefore, understanding the peculiarities of the mechanisms underlying the pathogenesis of this disease is of great importance for effective therapy of coronavirus disease 2019 (COVID-19). AIM: Analysis of the current data on HIF-1á and its effect on the pathogenesis and progression of COVID-19. The analysis of the relevant domestic and international literature sources was performed in the following sections: HIF-1á as a key factor of adaptation to hypoxia, targets for HIF-1á in the aspect of the pathogenesis of COVID-19, disorders in HIF-1á-mediated adaptation to hypoxia as an element of the pathogenesis of hyperactivation of the immune cells. CONCLUSION: HIF-1á prevents penetration of SARS-CoV-2 virus into a cell and primarily acts as the main regulator of the proinflammatory activity at the inflammation site surrounded by hypoxia. In the conditions of the deranged metabolic flexibility, a high level of HIF-1á evokes an excessive inflammatory response of the immune cells. A high HIF-1á level in cells of the inflammation focus is associated with enhanced production of the factors of angiogenesis mediating vascular permeability and capillary leakage process. This is accompanied by tissue damage and organ failure. At the same time, HIF-1á can mediate the anti-inflammatory effect through activation of adenosine receptor-dependent pathway, which is considered as a probable protection of cells and organs against damage by hyperactive immune cells.
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低氧诱导因子 1α 在 2019 年新型冠状病毒疾病发病机制中适应低氧的作用
简介:2019 年 12 月,一种新型冠状病毒(严重急性呼吸系统综合征相关冠状病毒 2(SARS-CoV-2))出现,并迅速在全球蔓延,引发了一场呼吸道疾病大流行。这种高致病性病毒可侵袭肺组织,使气体交换失常,导致急性呼吸窘迫综合征和全身缺氧。缺氧条件会引发适应机制的激活,包括缺氧诱导因子-1á(HIF-1á),它参与调节细胞的增殖、代谢和血管生成等关键过程。此外,HIF-1á 的表达水平与机体免疫反应的强度有关,包括先天免疫介导的炎症反应。因此,了解该疾病发病机制的特殊性对于有效治疗 2019 年冠状病毒病(COVID-19)具有重要意义。目的:分析目前关于HIF-1á及其对COVID-19发病机制和进展影响的数据。下文将对国内外相关文献资料进行分析:HIF-1á作为适应缺氧的关键因素、HIF-1á在COVID-19发病机制方面的靶点、HIF-1á介导的适应缺氧的紊乱作为免疫细胞过度激活发病机制的一个要素。结论:HIF-1á 能阻止 SARS-CoV-2 病毒穿透细胞,在缺氧环境下的炎症部位,它是促炎活动的主要调节器。在新陈代谢灵活性失调的情况下,高水平的 HIF-1á 会引起免疫细胞过度的炎症反应。炎症病灶细胞中的高水平 HIF-1á 与介导血管通透性和毛细血管渗漏过程的血管生成因子的生成增强有关。随之而来的是组织损伤和器官衰竭。与此同时,HIF-1á 还能通过激活腺苷受体依赖途径介导抗炎作用,这被认为是一种可能的保护细胞和器官免受过度活跃的免疫细胞损伤的方法。
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