Di-Tyrosine Crosslinking and <i>NOX4</i> Expression as Oxidative Pathological Markers in the Lungs of Patients with Idiopathic Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) is a noninflammatory progressive lung disease. Oxidative damage is a hallmark of IPF, but the sources and consequences of oxidant generation in the lungs are unclear. In this study, we addressed the link between the H<sub>2</sub>O<sub>2</sub&g...

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Autores principales: Sanja Blaskovic, Yves Donati, Isabelle Ruchonnet-Metrailler, Tamara Seredenina, Karl-Heinz Krause, Jean-Claude Pache, Dan Adler, Constance Barazzone-Argiroffo, Vincent Jaquet
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/e4be938dd67342a1870aef9678a650fd
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Sumario:Idiopathic pulmonary fibrosis (IPF) is a noninflammatory progressive lung disease. Oxidative damage is a hallmark of IPF, but the sources and consequences of oxidant generation in the lungs are unclear. In this study, we addressed the link between the H<sub>2</sub>O<sub>2</sub>-generating enzyme NADPH oxidase 4 (<i>NOX4</i>) and di-tyrosine (DT), an oxidative post-translational modification in IPF lungs. We performed immunohistochemical staining for DT and <i>NOX4</i> in pulmonary tissue from patients with IPF and controls using validated antibodies. In the healthy lung, DT showed little or no staining and <i>NOX4</i> was mostly present in normal vascular endothelium. On the other hand, both markers were detected in several cell types in the IPF patients, including vascular smooth muscle cells and epithelium (bronchial cells and epithelial cells type II). The link between <i>NOX4</i> and DT was addressed in human fibroblasts deficient for <i>NOX4</i> activity (mutation in the <i>CYBA</i> gene). Induction of <i>NOX4</i> by Transforming growth factor beta 1 (TGFβ1) in fibroblasts led to moderate DT staining after the addition of a heme-containing peroxidase in control cells but not in the fibroblasts deficient for <i>NOX4</i> activity. Our data indicate that DT is a histological marker of IPF and that <i>NOX4</i> can generate a sufficient amount of H<sub>2</sub>O<sub>2</sub> for DT formation in vitro.