Department of Pathology and Laboratory Medicine, Larner College of Medicine, University of Vermont, Burlington, Vermont.
Antioxid Redox Signal. 2019 Nov 10;31(14):1070-1091. doi: 10.1089/ars.2019.7752. Epub 2019 Apr 5.
The lung is a unique organ, as it is constantly exposed to air, and thus it requires a robust antioxidant defense system to prevent the potential damage from exposure to an array of environmental insults, including oxidants. The peroxiredoxin (PRDX) family plays an important role in scavenging peroxides and is critical to the cellular antioxidant defense system. Exciting discoveries have been made to highlight the key features of PRDXs that regulate the redox tone. PRDXs do not act in isolation as they require the thioredoxin/thioredoxin reductase/NADPH, sulfiredoxin (SRXN1) redox system, and in some cases glutaredoxin/glutathione, for their reduction. Furthermore, the chaperone function of PRDXs, controlled by the oxidation state, demonstrates the versatility in redox regulation and control of cellular biology exerted by this class of proteins. Despite the long-known observations that redox perturbations accompany a number of pulmonary diseases, surprisingly little is known about the role of PRDXs in the etiology of these diseases. In this perspective, we review the studies that have been conducted thus far to address the roles of PRDXs in lung disease, or experimental models used to study these diseases. Intriguing findings, such as the secretion of PRDXs and the formation of autoantibodies, raise a number of questions about the pathways that regulate secretion, redox status, and immune response to PRDXs. Further understanding of the mechanisms by which individual PRDXs control lung inflammation, injury, repair, chronic remodeling, and cancer, and the importance of PRDX oxidation state, configuration, and client proteins that govern these processes is needed.
肺是一个独特的器官,因为它不断暴露在空气中,因此需要一个强大的抗氧化防御系统来防止暴露于一系列环境刺激物(包括氧化剂)所带来的潜在损害。过氧化物酶(PRDX)家族在清除过氧化物方面发挥着重要作用,是细胞抗氧化防御系统的关键。令人兴奋的发现已经揭示了 PRDX 调节氧化还原状态的关键特征。PRDX 并非孤立发挥作用,因为它们的还原需要硫氧还蛋白/硫氧还蛋白还原酶/NADPH、硫氧还蛋白(SRXN1)氧化还原系统,在某些情况下还需要谷氧还蛋白/谷胱甘肽。此外,PRDX 的伴侣功能受氧化状态控制,这表明该类蛋白在氧化还原调节和控制细胞生物学方面具有多功能性。尽管人们早就观察到氧化还原波动伴随着许多肺部疾病,但令人惊讶的是,人们对 PRDX 在这些疾病发病机制中的作用知之甚少。在这篇观点文章中,我们回顾了迄今为止为探讨 PRDX 在肺部疾病中的作用或用于研究这些疾病的实验模型而进行的研究。一些有趣的发现,如 PRDX 的分泌和自身抗体的形成,提出了许多关于调节分泌、氧化还原状态和对 PRDX 免疫反应的途径的问题。需要进一步了解单个 PRDX 如何控制肺部炎症、损伤、修复、慢性重塑和癌症,以及 PRDX 氧化状态、构象和控制这些过程的客户蛋白的重要性。