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      Dynamic NETosis is Carried Out by Live Neutrophils in Human and Mouse Bacterial Abscesses and During Severe Gram-Positive Infection

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          Abstract

          Neutrophil extracellular traps (NETs) are released, as neutrophils die in vitro, in a process requiring hours, leaving a temporal gap for invasive microbes to exploit. Functional neutrophils undergoing NETosis have not been documented. During Gram-positive skin infections, we directly visualized live PMN in vivo rapidly releasing NETs, which prevented bacterial dissemination. NETosis occurred during crawling thereby casting large areas of NETs. NET-releasing PMN developed diffuse decondensed nuclei ultimately becoming devoid of DNA. Cells with abnormal nuclei displayed unusual crawling behavior highlighted by erratic pseudopods and hyperpolarization consistent with the nucleus being a fulcrum for crawling. A combined requirement of Tlr2 and complement mediated opsonization tightly regulated NET release. Additionally live human PMN developed decondensed nuclei and formed NETS in vivo and intact anuclear neutrophils were abundant in Gram-positive human abscesses. Therefore early in infection, non-cell death NETosis occurs in vivo during Gram-positive infection in mice and humans.

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          Most cited references50

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          Neutrophil extracellular traps kill bacteria.

          Neutrophils engulf and kill bacteria when their antimicrobial granules fuse with the phagosome. Here, we describe that, upon activation, neutrophils release granule proteins and chromatin that together form extracellular fibers that bind Gram-positive and -negative bacteria. These neutrophil extracellular traps (NETs) degrade virulence factors and kill bacteria. NETs are abundant in vivo in experimental dysentery and spontaneous human appendicitis, two examples of acute inflammation. NETs appear to be a form of innate response that binds microorganisms, prevents them from spreading, and ensures a high local concentration of antimicrobial agents to degrade virulence factors and kill bacteria.
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            Platelet TLR4 activates neutrophil extracellular traps to ensnare bacteria in septic blood.

            It has been known for many years that neutrophils and platelets participate in the pathogenesis of severe sepsis, but the inter-relationship between these players is completely unknown. We report several cellular events that led to enhanced trapping of bacteria in blood vessels: platelet TLR4 detected TLR4 ligands in blood and induced platelet binding to adherent neutrophils. This led to robust neutrophil activation and formation of neutrophil extracellular traps (NETs). Plasma from severely septic humans also induced TLR4-dependent platelet-neutrophil interactions, leading to the production of NETs. The NETs retained their integrity under flow conditions and ensnared bacteria within the vasculature. The entire event occurred primarily in the liver sinusoids and pulmonary capillaries, where NETs have the greatest capacity for bacterial trapping. We propose that platelet TLR4 is a threshold switch for this new bacterial trapping mechanism in severe sepsis.
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              Netting neutrophils in autoimmune small-vessel vasculitis.

              Small-vessel vasculitis (SVV) is a chronic autoinflammatory condition linked to antineutrophil cytoplasm autoantibodies (ANCAs). Here we show that chromatin fibers, so-called neutrophil extracellular traps (NETs), are released by ANCA-stimulated neutrophils and contain the targeted autoantigens proteinase-3 (PR3) and myeloperoxidase (MPO). Deposition of NETs in inflamed kidneys and circulating MPO-DNA complexes suggest that NET formation triggers vasculitis and promotes the autoimmune response against neutrophil components in individuals with SVV.
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                Author and article information

                Journal
                9502015
                8791
                Nat Med
                Nat. Med.
                Nature medicine
                1078-8956
                1546-170X
                28 June 2013
                September 2012
                07 August 2015
                : 18
                : 9
                : 1386-1393
                Affiliations
                [1 ]Department of Critical Care Medicine, University of Calgary, Canada
                [2 ]The Calvin, Phoebe and Joan Snyder Institute for Chronic Diseases, University of Calgary, Canada
                [3 ]Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Canada
                [4 ]Department of Pathology and Laboratory Medicine, University of Calgary, Canada
                [5 ]Department of Physiology and Biophysics, University of Calgary, Canada
                [6 ]Department of Medicine, University of Calgary, Canada
                [7 ]Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut, USA
                [8 ]Centre d’Ecologie Cellulaire, Hôpital de la Salpétrière, Paris, France
                Author notes
                Corresponding author: Dr. Paul Kubes. HRIC 4AA16, 3330 Hospital Drive NW, Calgary, AB, Canada T2N 4N1. tel 403-220-8558, fax 403-270-7516. pkubes@ 123456ucalgary.ca
                [9]

                These authors contributed equally.

                Article
                NIHMS487969
                10.1038/nm.2847
                4529131
                22922410
                1b7be7fd-e132-4264-a01c-d251c7ac6d04
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                Medicine
                Medicine

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