Department of Pharmacology, The University of Melbourne, Parkville, VIC, Australia.
Am J Respir Cell Mol Biol. 2013 Jan;48(1):17-26. doi: 10.1165/rcmb.2011-0345OC. Epub 2012 Sep 20.
Oxidative stress caused by excessive reactive oxygen species production is implicated in influenza A virus-induced lung disease. Glutathione peroxidase (GPx)-1 is an antioxidant enzyme that may protect lungs from such damage. The objective of this study was to determine if GPx-1 protects the lung against influenza A virus-induced lung inflammation in vivo. Male wild-type (WT) or GPx-1(-/-) mice were inoculated with HKx31 (H3N2, 1 × 10(4) plaque-forming units), and bronchoalveolar lavage fluid (BALF)/lung compartments were analyzed on Days 3 and 7 after infection for inflammatory marker expression, histology, and viral titer. WT mice infected with HKx31 had significantly more BALF total cells, macrophages, neutrophils, and lymphocytes at Days 3 and 7 compared with naive WT animals (n = 5-8; P < 0.05). However, infected GPx-1(-/-) mice had significantly more BALF inflammation, which included more total cells, macrophages, and neutrophils, compared with WT mice, and this was abolished by treatment with the GPx mimetic ebselen. BALF inflammation persisted in GPx-1(-/-) mice on Day 10 after infection, and GPx-1(-/-) mice had significantly more influenza-specific CD8(+) T cells in spleen compared with WT mice (n = 3-4; P < 0.05). Infected GPx-1(-/-) mice had greater peribronchial and parenchymal inflammation than WT mice, and viral titer was significantly reduced in GPx-1(-/-) mice at Day 3 (n = 5; P < 0.05). Gene expression analysis revealed that infected GPx-1(-/-) mice had higher whole lung TNF-α, macrophage inflammatory protein (MIP)-1α, MIP-2, KC, and matrix metalloproteinase (MMP)-12 mRNA compared with infected WT mice. GPx-1(-/-) mice had more MIP-2 protein in BALF at Day 3 and more active MMP-9 protease in BALF at Days 3 and 7 than WT mice. These data indicate that GPx-1 reduces influenza A virus-induced lung inflammation.
活性氧(ROS)的产生过多导致的氧化应激与甲型流感病毒(IAV)诱导的肺病有关。谷胱甘肽过氧化物酶 1(GPx-1)是一种抗氧化酶,可能保护肺部免受这种损伤。本研究的目的是确定 GPx-1 是否能在体内保护肺免受 IAV 诱导的肺炎症。雄性野生型(WT)或 GPx-1(-/-)小鼠用 HKx31(H3N2,1×10(4)噬菌斑形成单位)接种,并在感染后第 3 和第 7 天分析支气管肺泡灌洗液(BALF)/肺隔室的炎症标志物表达、组织学和病毒滴度。与野生型 WT 动物(n = 5-8;P < 0.05)相比,感染 HKx31 的 WT 小鼠在第 3 和第 7 天 BALF 中的总细胞、巨噬细胞、中性粒细胞和淋巴细胞明显更多。然而,与 WT 小鼠相比,感染的 GPx-1(-/-)小鼠的 BALF 炎症明显更多,包括更多的总细胞、巨噬细胞和中性粒细胞,并且这种炎症可以通过 GPx 模拟物 ebselen 治疗来消除。感染后的第 10 天,GPx-1(-/-)小鼠的 BALF 炎症仍然持续存在,并且与 WT 小鼠相比,GPx-1(-/-)小鼠的脾中流感特异性 CD8(+)T 细胞明显更多(n = 3-4;P < 0.05)。与 WT 小鼠相比,感染的 GPx-1(-/-)小鼠的细支气管和实质周围炎症更严重,并且在第 3 天病毒滴度明显降低(n = 5;P < 0.05)。基因表达分析显示,与感染 WT 小鼠相比,感染的 GPx-1(-/-)小鼠的整个肺 TNF-α、巨噬细胞炎症蛋白(MIP)-1α、MIP-2、KC 和基质金属蛋白酶(MMP)-12 mRNA 水平更高。与 WT 小鼠相比,GPx-1(-/-)小鼠在第 3 天的 BALF 中具有更高的 MIP-2 蛋白水平,并且在第 3 和第 7 天的 BALF 中具有更多的活性 MMP-9 蛋白酶。这些数据表明,GPx-1 可减轻 IAV 诱导的肺炎症。