NADPH oxidase 4 is protective and not fibrogenic in intestinal inflammation

• Published in: Redox biology 2020-10, Vol.37, p.101752-101752, Article 101752
• Main Authors: Stenke, Emily, Aviello, Gabriella, Singh, Ashish, Martin, Sean, Winter, Des, Sweeney, Brian, McDermott, Michael, Bourke, Billy, Hussey, Seamus, Knaus, Ulla G.
• Format: Article
• Language: English
• Subjects: Crohn's disease; Fibrosis; Intestinal inflammation; NADPH oxidase; NOX4; Research Paper
• ISSN: 2213-2317; 2213-2317
• DOI: 10.1016/j.redox.2020.101752

Dysregulated redox signaling and oxidative injury are associated with inflammatory processes and fibrosis. H2O2 generation by NOX4 has been suggested as a key driver in the development of fibrosis and a small molecule drug is under evaluation in clinical trials for idiopathic pulmonary fibrosis and primary biliary cholangitis. Fibrosis is a common complication in Crohn's disease (CD) leading to stricture formation in 35–40% of patients, who require surgical interventions in the absence of therapeutic options. Here we assess NOX4 expression in CD patients with inflammatory or stricturing disease and examine whether loss of NOX4 is beneficial in acute and fibrotic intestinal disease. NOX4 was upregulated in inflamed mucosal tissue of CD and ulcerative colitis (UC) patients, in CD ileal strictures, and in mice with intestinal inflammation. Nox4 deficiency in mice promoted pathogen colonization and exacerbated tissue injury in acute bacterial and chemical colitis. In contrast, in two chronic injury models aberrant tissue remodeling and fibrosis-related gene expression did not differ substantially between Nox4−/− mice and wildtype mice, suggesting that Nox4 is dispensable in TGF-β1-driven intestinal fibrogenesis. While animal models do not recapitulate all the hallmarks of CD fibrosis, the tissue-protective role of Nox4 warrants a cautious approach to pharmacological inhibitors. [Display omitted] •NOX4 is elevated in inflammatory bowel disease strictures and inflamed biopsies.•Murine intestinal fibrogenesis is not dependent on Nox4.•Nox4 is protective in acute murine colitis.