| Literature DB >> 31422870 |
Luis E Muñoz1, Sebastian Boeltz1, Rostyslav Bilyy2, Christine Schauer1, Aparna Mahajan1, Navena Widulin3, Anika Grüneboom1, Irmgard Herrmann1, Edgyda Boada4, Manfred Rauh5, Veit Krenn6, Mona H C Biermann1, Malgorzata J Podolska1, Jonas Hahn1, Jasmin Knopf1, Christian Maueröder1, Solomiya Paryzhak7, Tetiana Dumych7, Yi Zhao8, Markus F Neurath9, Markus H Hoffmann1, Tobias A Fuchs10, Moritz Leppkes9, Georg Schett1, Martin Herrmann11.
Abstract
The presence of gallstones (cholelithiasis) is a highly prevalent and severe disease and one of the leading causes of hospital admissions worldwide. Due to its substantial health impact, we investigated the biological mechanisms that lead to the formation and growth of gallstones. We show that gallstone assembly essentially requires neutrophil extracellular traps (NETs). We found consistent evidence for the presence of NETs in human and murine gallstones and describe an immune-mediated process requiring activation of the innate immune system for the formation and growth of gallstones. Targeting NET formation via inhibition of peptidyl arginine deiminase type 4 or abrogation of reactive oxygen species (ROS) production, as well as damping of neutrophils by metoprolol, effectively inhibit gallstone formation in vivo. Our results show that after the physicochemical process of crystal formation, NETs foster their assembly into larger aggregates and finally gallstones. These insights provide a feasible therapeutic concept to prevent cholelithiasis in patients at risk.Entities:
Keywords: NOX2; PADi4; calcium carbonate crystals; cholesterol crystals; gallstone growth; gallstones; lisosomal leakage; lithogenic diet; neutrophil extracellular traps; neutrophils
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Year: 2019 PMID: 31422870 DOI: 10.1016/j.immuni.2019.07.002
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745