The Fatal Circle of NETs and NET-Associated DAMPs Contributing to Organ Dysfunction

被引:49
作者
Block, Helena [1 ]
Rossaint, Jan [1 ]
Zarbock, Alexander [1 ]
机构
[1] Univ Hosp Muenster, Dept Anesthesiol Intens Care & Pain Med, D-48149 Munster, Germany
关键词
neutrophil extracellular traps; damage associated molecular pattern; inflammation; innate immune response; remote organ damage; HMGB1; LL37; histone; cfDNA; CIRP; NEUTROPHIL EXTRACELLULAR TRAPS; ANTIMICROBIAL PEPTIDE LL-37; GROUP BOX 1; ACUTE LUNG INJURY; MITOCHONDRIAL-DNA; DENDRITIC CELLS; INNATE IMMUNITY; MICROSCOPIC POLYANGIITIS; INFLAMMATORY RESPONSES; C1-ESTERASE INHIBITOR;
D O I
10.3390/cells11121919
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The innate immune system is the first line of defense against invading pathogens or sterile injuries. Pattern recognition receptors (PRR) sense molecules released from inflamed or damaged cells, or foreign molecules resulting from invading pathogens. PRRs can in turn induce inflammatory responses, comprising the generation of cytokines or chemokines, which further induce immune cell recruitment. Neutrophils represent an essential factor in the early immune response and fulfill numerous tasks to fight infection or heal injuries. The release of neutrophil extracellular traps (NETs) is part of it and was originally attributed to the capture and elimination of pathogens. In the last decade studies revealed a detrimental role of NETs during several diseases, often correlated with an exaggerated immune response. Overwhelming inflammation in single organs can induce remote organ damage, thereby further perpetuating release of inflammatory molecules. Here, we review recent findings regarding damage-associated molecular patterns (DAMPs) which are able to induce NET formation, as well as NET components known to act as DAMPs, generating a putative fatal circle of inflammation contributing to organ damage and sequentially occurring remote organ injury.
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页数:26
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共 241 条
[1]   Cutting edge: HMG-1 as a mediator of acute lung inflammation [J].
Abraham, E ;
Arcaroli, J ;
Carmody, A ;
Wang, HC ;
Tracey, KJ .
JOURNAL OF IMMUNOLOGY, 2000, 165 (06) :2950-2954
[2]   Pulmonary Vascular Endothelialitis, Thrombosis, and Angiogenesis in Covid-19 [J].
Ackermann, Maximilian ;
Verleden, Stijn E. ;
Kuehnel, Mark ;
Haverich, Axel ;
Welte, Tobias ;
Laenger, Florian ;
Vanstapel, Arno ;
Werlein, Christopher ;
Stark, Helge ;
Tzankov, Alexandar ;
Li, William W. ;
Li, Vincent W. ;
Mentzer, Steven J. ;
Jonigk, Danny .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 383 (02) :120-128
[3]   Thrombosis risk associated with COVID-19 infection. A scoping review [J].
Al-Ani, Fatimah ;
Chehade, Samer ;
Lazo-Langner, Alejro .
THROMBOSIS RESEARCH, 2020, 192 :152-160
[4]   Superoxide Induces Neutrophil Extracellular Trap Formation in a TLR-4 and NOX-Dependent Mechanism [J].
Al-Khafaji, Ahmed B. ;
Tohme, Samer ;
Yazdani, Hamza Obaid ;
Miller, David ;
Huang, Hai ;
Tsung, Allan .
MOLECULAR MEDICINE, 2016, 22 :621-631
[5]   Circulating Histones Are Major Mediators of Cardiac Injury in Patients With Sepsis [J].
Alhamdi, Yasir ;
Abrams, Simon T. ;
Cheng, Zhenxing ;
Jing, Shengjie ;
Su, Dunhao ;
Liu, Zhiyong ;
Lane, Steven ;
Welters, Ingeborg ;
Wang, Guozheng ;
Toh, Cheng-Hock .
CRITICAL CARE MEDICINE, 2015, 43 (10) :2094-2103
[6]   High frequency of venous thromboembolic events in Churg-Strauss syndrome, Wegener's granulomatosis and microscopic polyangiitis but not polyarteritis nodosa: a systematic retrospective study on 1130 patients [J].
Allenbach, Y. ;
Seror, R. ;
Pagnoux, C. ;
Teixeira, L. ;
Guilpain, P. ;
Guillevin, L. .
ANNALS OF THE RHEUMATIC DISEASES, 2009, 68 (04) :564-567
[7]   Pattern Recognition Receptors and the Host Cell Death Molecular Machinery [J].
Amarante-Mendes, Gustavo P. ;
Adjemian, Sandy ;
Branco, Laura Migliari ;
Zanetti, Larissa C. ;
Weinlich, Ricardo ;
Bortoluci, Karina R. .
FRONTIERS IN IMMUNOLOGY, 2018, 9
[8]   Extracellular histones increase plasma thrombin generation by impairing thrombomodulin-dependent protein C activation [J].
Ammollo, C. T. ;
Semeraro, F. ;
Xu, J. ;
Esmon, N. L. ;
Esmon, C. T. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 (09) :1795-1803
[9]   Cell-Cycle Proteins Control Production of Neutrophil Extracellular Traps [J].
Amulic, Borko ;
Knackstedt, Sebastian Lorenz ;
Abu Abed, Ulrike ;
Deigendesch, Nikolaus ;
Harbort, Christopher J. ;
Caffrey, Brian E. ;
Brinkmann, Volker ;
Heppner, Frank L. ;
Hinds, Philip W. ;
Zychlinsky, Arturo .
DEVELOPMENTAL CELL, 2017, 43 (04) :449-+
[10]   Cutting Edge: Antimalarial Drugs Inhibit IFN-β Production through Blockade of Cyclic GMP-AMP Synthase-DNA Interaction [J].
An, Jie ;
Woodward, Joshua J. ;
Sasaki, Tomikazu ;
Minie, Mark ;
Elkon, Keith B. .
JOURNAL OF IMMUNOLOGY, 2015, 194 (09) :4089-4093