Frise Matthew C, Robbins Peter A
Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.
Exp Physiol. 2015 Nov;100(11):1233-41. doi: 10.1113/expphysiol.2014.080507. Epub 2014 Oct 18.
What is the topic of this review? This review is principally concerned with results from studies of the pulmonary vasculature in humans, particularly in relation to hypoxia and rare diseases that affect oxygen sensing. What advances does it highlight? This review highlights the degree to which the hypoxia-inducible factor (HIF) transcription system influences human pulmonary vascular responses to hypoxia. Upregulation of the HIF pathway augments hypoxic pulmonary vasoconstriction, while alterations to the pathway found in Tibetans are associated with suppression of the progressive increase in pulmonary artery pressure with sustained hypoxia. It also highlights the potential importance of iron, which modulates the HIF pathway, in modifying the pulmonary vascular response to hypoxia. The human pulmonary circulation loses its natural distensibility during sustained hypoxia, leading to pulmonary arterial hypertension and a much higher workload for the right ventricle. The hypoxia-inducible factor (HIF) pathway is implicated in this pulmonary vascular response to continued hypoxia by animal studies, and additionally, by rare human diseases where the pathway is upregulated. However, there are no known human genetic diseases downregulating HIF. Tibetans, though, demonstrate blunted pulmonary vascular responses to sustained hypoxia. This seems to be accounted for by an altered HIF pathway as a consequence of natural selection over a period of many thousands of years lived at high altitude. In addition to genetic differences, iron is another important modulator of HIF pathway function. Experimental work in humans demonstrates that manipulation of iron stores can influence the behaviour of the pulmonary circulation during hypoxia, in ways analogous to that seen in Tibetans and patients with rare diseases that affect oxygen sensing. The importance of physiological differences in iron bioavailability in modulating hypoxic pulmonary vasoconstriction in health and disease is yet to be established.
本综述的主题是什么?本综述主要关注人类肺血管系统的研究结果,特别是与缺氧以及影响氧感知的罕见疾病相关的研究结果。它突出了哪些进展?本综述强调了缺氧诱导因子(HIF)转录系统对人类肺血管对缺氧反应的影响程度。HIF途径的上调增强了缺氧性肺血管收缩,而在藏族人群中发现的该途径的改变与持续缺氧时肺动脉压力的渐进性升高受到抑制有关。它还强调了铁在调节肺血管对缺氧反应中的潜在重要性,铁可调节HIF途径。在持续缺氧期间,人类肺循环会失去其天然的扩张能力,导致肺动脉高压和右心室的工作负荷大幅增加。动物研究以及一些该途径上调的罕见人类疾病表明,缺氧诱导因子(HIF)途径参与了肺血管对持续缺氧的反应。然而,目前尚无已知的下调HIF的人类遗传疾病。不过,藏族人群对持续缺氧的肺血管反应较为迟钝。这似乎是由于在数千年的高海拔生活中自然选择导致HIF途径发生改变所致。除了遗传差异外,铁是HIF途径功能的另一个重要调节因子。人体实验工作表明,控制铁储备可以影响缺氧时肺循环的表现,其方式类似于藏族人群和患有影响氧感知的罕见疾病的患者。铁生物利用度的生理差异在调节健康和疾病状态下的缺氧性肺血管收缩中的重要性尚未确定。