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Article Abstract

is a parasitic trematode that causes fasciolosis in sheep, provoking a decrease in their reproductive capacity, weight gain, meat and milk production, and wool quality. In the pathogenesis of , the penetration and migration of parasitic stages through the liver provoke intense inflammatory immune responses and tissue damage. The aim of this study was to investigate the cytotoxic effects of -induced ovine NETs in exposed hepatocytes in vitro, and to analyze whether antigens (Ag) trigger the release of ovine NETs under hypoxic conditions as well as the roles of matrix metalloproteinase-9 (MMP-9) and CD11b in this cellular process in vitro. Here, isolated ovine PMNs were co-cultured with Ag under hypoxia (5% O) and NETs were visualized via immunofluorescence analyses, confirming their classical characteristics. The quantification of NETs in response to Ag in hypoxic conditions significantly enhanced the formation of anchored and cell-free NETs ( < 0.01), and NADPH oxidase (NOX) inhibitor diphenylene iodonium (DPI) significantly reduced their production ( < 0.05). Furthermore, the cytotoxic effect of NETs on hepatic cells was determined by using a live/dead-staining with Sytox Orange, thereby demonstrating that Ag-induced NETs are cytotoxic for hepatic cells ( = 0.001). We additionally analyzed PMN supernatants to determine the enzymatic activity of MMP-9, observing that Ag exposure enhances MMP-9 release in ovine PMNs ( < 0.05) but not in bovine PMNs. Interestingly, by using flow cytometric analysis, we determined that the exposure of PMNs to Ag does not increase the CD11b surface expression of ovine PMNs. This could be an effect of the activation of other surface receptors or transcription factors involved in -induced NETosis. Consequently, we hypothesize that -induced NETs play a role in the pathogenesis of fasciolosis, contributing to liver tissue damage if released in an uncontrolled manner.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11640480PMC
http://dx.doi.org/10.3390/ani14233456DOI Listing

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