Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan 48824, USA.
Am J Physiol Lung Cell Mol Physiol. 2012 Mar 1;302(5):L455-62. doi: 10.1152/ajplung.00193.2011. Epub 2011 Dec 16.
Allergic airway disease is characterized by a T helper type 2 cell-mediated airway inflammation and airway hyperresponsiveness. Little is known about the role of hypoxia-mediated signaling in the progression of the disease. To address this knowledge gap, a mouse model was created in which doxycycline exposure induces the functional deletion of hypoxia inducible factor-1α from alveolar type II and Clara cells of the lung. When hypoxia inducible factor-1α deletion was induced during the early postnatal development period of the lung, the mice displayed an enhanced response to the ovalbumin model of allergic airway disease. These hypoxia inducible factor-1α-deficient mice exhibit increased cellular infiltrates, eosinophilia in the lavage fluid and parenchyma, and T helper type 2 cytokines, as compared with ovalbumin-treated control mice. Moreover, these hypoxia inducible factor-1α-deficient mice display increased airway resistance when compared with their control counterparts. Interestingly, if the loss of hypoxia inducible factor-1α was induced in early adulthood, the exacerbated phenotype was not observed. Taken together, these results suggest that epithelial hypoxia inducible factor-1α plays an important role in establishing the innate immunity of the lung and epithelial-specific deficiency in the transcription factor, during early postnatal development, increases the severity of inflammation and functional airway resistance, following ovalbumin challenge. Finally, these results might explain some of the chronic respiratory pathology observed in premature infants, especially those that receive supplemental oxygen. This early hyperoxic exposure, from normal ambient and supplemental oxygen, would presumably inhibit normal hypoxia inducible factor-1α signaling, mimicking the functional deletion described.
过敏性气道疾病的特征是 T 辅助细胞 2 型细胞介导的气道炎症和气道高反应性。关于缺氧介导的信号在疾病进展中的作用知之甚少。为了解决这一知识空白,创建了一种小鼠模型,其中强力霉素暴露诱导肺泡 II 型和 Clara 细胞中的缺氧诱导因子-1α的功能缺失。当在肺的早期出生后发育期间诱导缺氧诱导因子-1α缺失时,小鼠对卵清蛋白诱导的过敏性气道疾病模型表现出增强的反应。与卵清蛋白处理的对照小鼠相比,这些缺氧诱导因子-1α缺陷小鼠显示出增加的细胞浸润、灌洗液和实质中的嗜酸性粒细胞增多以及 T 辅助细胞 2 细胞因子。此外,与对照小鼠相比,这些缺氧诱导因子-1α缺陷小鼠显示出增加的气道阻力。有趣的是,如果在成年早期诱导缺氧诱导因子-1α的丧失,则不会观察到加剧的表型。总之,这些结果表明上皮缺氧诱导因子-1α在建立肺的先天免疫中起重要作用,并且在早期出生后发育期间,转录因子的上皮特异性缺失增加了炎症和功能性气道阻力的严重程度,在卵清蛋白挑战后。最后,这些结果可能解释了早产儿中观察到的一些慢性呼吸道病理学,特别是那些接受补充氧气的早产儿。这种早期的高氧暴露,来自正常的环境和补充氧气,大概会抑制正常的缺氧诱导因子-1α信号,模拟所描述的功能缺失。