| Literature DB >> 34941394 |
Lakmali M Silva1,2, Andrew D Doyle3, Teresa Greenwell-Wild2, Nicolas Dutzan2,4, Collin L Tran1, Loreto Abusleme2,5, Lih Jiin Juang6, Jerry Leung6, Elizabeth M Chun1, Andrew G Lum2, Cary S Agler7, Carlos E Zuazo2, Megan Sibree1, Priyam Jani8, Vardit Kram8, Daniel Martin9, Kevin Moss7, Michail S Lionakis10, Francis J Castellino11, Christian J Kastrup6,12,13, Matthew J Flick14, Kimon Divaris15,16, Thomas H Bugge1, Niki M Moutsopoulos2.
Abstract
Tissue-specific cues are critical for homeostasis at mucosal barriers. Here, we report that the clotting factor fibrin is a critical regulator of neutrophil function at the oral mucosal barrier. We demonstrate that commensal microbiota trigger extravascular fibrin deposition in the oral mucosa. Fibrin engages neutrophils through the αMβ2 integrin receptor and activates effector functions, including the production of reactive oxygen species and neutrophil extracellular trap formation. These immune-protective neutrophil functions become tissue damaging in the context of impaired plasmin-mediated fibrinolysis in mice and humans. Concordantly, genetic polymorphisms in PLG, encoding plasminogen, are associated with common forms of periodontal disease. Thus, fibrin is a critical regulator of neutrophil effector function, and fibrin-neutrophil engagement may be a pathogenic instigator for a prevalent mucosal disease.Entities:
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Year: 2021 PMID: 34941394 DOI: 10.1126/science.abl5450
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728