Heme-related molecules induce rapid production of neutrophil extracellular traps

Transfusion

Volumn 54, Issue 11, 2014, Pages 2811-2819

  Kono, Mari ^a   Saigo, Katsuyasu ^b   Takagi, Yuri ^a   Takahashi, Takayuki ^c   Kawauchi, Sawako ^a   Wada, Atsushi ^a   Hashimoto, Makoto ^d   Minami, Yosuke ^d   Imoto, Shion ^e   Takenokuchi, Mariko ^b   Morikawa, Takashi ^a   Funakoshi, Kunihiro ^a  

^a SYSMEX CORPORATION   (Japan)

^b HIMEJI DOKKYO UNIVERSITY   (Japan)

^c Shinko Hospital   (Japan)

^d KOBE UNIVERSITY HOSPITAL   (Japan)

^e KOBE TOKIWA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

APOCYNIN; DEFERASIROX; DEFEROXAMINE; HEMIN; HISTONE H3; MYELOPEROXIDASE; REACTIVE OXYGEN METABOLITE; HEME;

ARTICLE; BLOOD COMPONENT; CELL ISOLATION; CELL NUCLEUS MEMBRANE; CELL STRUCTURE; CONCENTRATION PROCESS; CONFOCAL LASER MICROSCOPY; DISEASE ASSOCIATION; ELECTRON MICROSCOPY; ENZYME LINKED IMMUNOSORBENT ASSAY; ERYTHROCYTE; HEMOLYSIS; HUMAN; HUMAN CELL; INCUBATION TIME; INHIBITION KINETICS; LEUKOCYTE ACTIVATION; NEUTROPHIL; NEUTROPHIL EXTRACELLULAR TRAP; PROTEIN BLOOD LEVEL; PROTEIN STRUCTURE; STAINING; TRANSFUSION RELATED ACUTE LUNG INJURY; TRANSMISSION ELECTRON MICROSCOPY; ACUTE LUNG INJURY; BLOOD TRANSFUSION; CLINICAL TRIAL; CONFOCAL MICROSCOPY; FEMALE; MALE; METABOLISM; MULTICENTER STUDY; PATHOLOGY; TIME;

ACUTE LUNG INJURY; BLOOD TRANSFUSION; FEMALE; HEME; HEMOLYSIS; HUMANS; MALE; MICROSCOPY, CONFOCAL; NEUTROPHILS; NUCLEAR ENVELOPE; REACTIVE OXYGEN SPECIES; TIME FACTORS;

EID: 84912559166     PISSN: 00411132     EISSN: 15372995     Source Type: Journal    
DOI: 10.1111/trf.12700     Document Type: Article

References (45)

1. Rubenfeld GD, Caldwell E, Peabody E, et al. Incidence and outcomes of acute lung injury. N Engl J Med 2005; 353: 1685-1693.
2. Luhr OR, Antonsen K, Karlsson M, et al. Incidence and mortality after acute respiratory failure and acute respiratory distress syndrome in Sweden, Denmark, and Iceland. The ARF Study Group. Am J Respir Crit Care Med 1999; 159: 1849-1861.
3. Villar J, Blanco J, Anon JM, et al. The ALIEN study: incidence and outcome of acute respiratory distress syndrome in the era of lung protective ventilation. Intensive Care Med 2011; 37: 1932-1941.
4. The Irish Critical Care Trials Group. Acute lung injury and the acute respiratory distress syndrome in Ireland: a prospective audit of epidemiology and management. Crit Care 2008; 12: R30.
5. Bernard GR, Artigas A, Brigham KL, et al. The American-European Consensus Conference on ARDS. Definitions, mechanisms, relevant outcomes, and clinical trial coordination. Am J Respir Crit Care Med 1994; 149: 818-824.
6. Singh NR, Johnson A, Peters AM, et al. Acute lung injury results from failure of neutrophil de-priming: a new hypothesis. Eur J Clin Invest 2012; 42: 1342-1349.
7. Holness L, Knippen MA, Simmons L, et al. Fatalities caused by TRALI. Transfus Med Rev 2004; 18: 184-188.
8. Triulzi DJ,. Transfusion-related acute lung injury: current concepts for the clinician. Anesth Analg 2009; 108: 770-776.
9. Shaz BH, Stowell SR, Hillyer CD,. Transfusion-related acute lung injury: from bedside to bench and back. Blood 2011; 117: 1463-1471.
10. Bux J,. Antibody-mediated (immune) transfusion-related acute lung injury. Vox Sang 2011; 100: 122-128.
11. Sachs UJ, Hattar K, Weissmann N, et al. Antibody-induced neutrophil activation as a trigger for transfusion-related acute lung injury in an ex vivo rat lung model. Blood 2006; 107: 1217-1219.
12. Khan SY, Kelher MR, Heal JM, et al. Soluble CD40 ligand accumulates in stored blood components, primes neutrophils through CD40, and is a potential cofactor in the development of transfusion-related acute lung injury. Blood 2006; 108: 2455-2462.
13. Silliman CC, Bjornsen AJ, Wyman TH, et al. Plasma and lipids from stored platelets cause acute lung injury in an animal model. Transfusion 2003; 43: 633-640.
14. Hishizawa M, Mitsuhashi R, Ohno T,. Transfusion-related acute lung injury (TRALI) induced by donor-derived anti-HLA antibodies in aplastic anemia: possible priming effect of granulocyte-colony stimulating factor (G-CSF) on the recipient neutrophils. Intern Med 2009; 48: 1979-1983.
15. Eder AF, Herron R, Strupp A, et al. Transfusion-related acute lung injury surveillance (2003-2005) and the potential impact of the selective use of plasma from male donors in the American Red Cross. Transfusion 2007; 47: 599-607.
16. Kono M, Saigo K, Takagi Y, et al. Morphological and flow-cytometric analysis of haemin-induced human neutrophil activation: implications for transfusion-related acute lung injury. Blood Transfus 2013; 11: 53-60.
17. Graca-Souza AV, Arruda MA, de Freitas MS, et al. Neutrophil activation by heme: implications for inflammatory processes. Blood 2002; 99: 4160-4165.
18. Porto BN, Alves LS, Fernandez PL, et al. Heme induces neutrophil migration and reactive oxygen species generation through signaling pathways characteristic of chemotactic receptors. J Biol Chem 2007; 282: 24430-24436.
19. Saigo K, Hashimoto M, Jyokei Y, et al. [Activation of human neutrophils by hemin]. Rinsho Byori 2008; 56: 967-972.
20. Zimmermann R, Wintzheimer S, Weisbach V, et al. Influence of prestorage leukoreduction and subsequent irradiation on in vitro red blood cell (RBC) storage variables of RBCs in additive solution saline-adenine-glucose-mannitol. Transfusion 2009; 49: 75-80.
21. Gandhi MJ, Shapiro E, Emmert L, et al. Prestorage leukoreduction does not increase hemolysis of stored red cell concentrates. Transfus Apher Sci 2007; 36: 17-22.
22. Ghosh S, Adisa OA, Chappa P, et al. Extracellular hemin crisis triggers acute chest syndrome in sickle mice. J Clin Invest 2013; 123: 4809-4820.
23. Orino K,. Functional binding analysis of human fibrinogen as an iron- and heme-binding protein. Biometals 2013; 26: 789-794.
24. Zunszain PA, Ghuman J, Komatsu T, et al. Crystal structural analysis of human serum albumin complexed with hemin and fatty acid. BMC Struct Biol 2003; 3: 6.
25. Djalali AG, Moore KA, Kelly E,. Report of a patient with severe transfusion-related acute lung injury after multiple transfusions, resuscitated with albumin. Resuscitation 2005; 66: 225-230.
26. Walter PB, Macklin EA, Porter J, et al. Inflammation and oxidant-stress in beta-thalassemia patients treated with iron chelators deferasirox (ICL670) or deferoxamine: an ancillary study of the Novartis CICL670A0107 trial. Haematologica 2008; 93: 817-825.
27. Zarogiannis SG, Jurkuvenaite A, Fernandez S, et al. Ascorbate and deferoxamine administration after chlorine exposure decrease mortality and lung injury in mice. Am J Respir Cell Mol Biol 2011; 45: 386-392.
28. Vlahakos D, Arkadopoulos N, Kostopanagiotou G, et al. Deferoxamine attenuates lipid peroxidation, blocks interleukin-6 production, ameliorates sepsis inflammatory response syndrome, and confers renoprotection after acute hepatic ischemia in pigs. Artif Organs 2012; 36: 400-408.
29. Kostopanagiotou GG, Kalimeris KA, Arkadopoulos NP, et al. Desferrioxamine attenuates minor lung injury following surgical acute liver failure. Eur Respir J 2009; 33: 1429-1436.
30. Saigo K, Kono M, Takagi Y, et al. Deferasirox reduces oxidative stress in patients with transfusion dependency. J. Clin Med Res 2013; 5: 57-60.
31. Thomas GM, Carbo C, Curtis BR, et al. Extracellular DNA traps are associated with the pathogenesis of TRALI in humans and mice. Blood 2012; 119: 6335-6343.
32. Caudrillier A, Kessenbrock K, Gilliss BM, et al. Platelets induce neutrophil extracellular traps in transfusion-related acute lung injury. J Clin Invest 2012; 122: 2661-2671.
33. Brinkmann V, Reichard U, Goosmann C, et al. Neutrophil extracellular traps kill bacteria. Science 2004; 303: 1532-1535.
34. Gardiner EE, Andrews RK,. Neutrophil extracellular traps (NETs) and infection-related vascular dysfunction. Blood Rev 2012; 26: 255-259.
35. Fuchs TA, Abed U, Goosmann C, et al. Novel cell death program leads to neutrophil extracellular traps. J Cell Biol 2007; 176: 231-241.
36. Brinkmann V, Zychlinsky A,. Beneficial suicide: why neutrophils die to make NETs. Nat Rev Microbiol 2007; 5: 577-582.
37. Pilsczek FH, Salina D, Poon KK, et al. A novel mechanism of rapid nuclear neutrophil extracellular trap formation in response to Staphylococcus aureus. J Immunol 2010; 185: 7413-7425.
38. Hirayama J, Abe H, Azuma H, et al. Leakage of potassium from red blood cells following gamma ray irradiation in the presence of dipyridamole, trolox, human plasma or mannitol. Biol Pharm Bull 2005; 28: 1318-1320.
39. Nakamura A, Abe K, Masuya M, et al. Efficiency of diversion of the first aliquot of blood and prestorage leukoreduction for preventing bacterial contamination in red blood cell concentrates assessed using a rapid polymerase chain reaction-based bacterial detection system. Transfus Med 2011; 21: 365-370.
40. Lombardo ME, Araujo LS, Ciccarelli AB, et al. A spectrophotometric method for estimating hemin in biological systems. Anal Biochem 2005; 341: 199-203.
41. Silliman CC, Ambruso DR, Boshkov LK,. Transfusion-related acute lung injury. Blood 2005; 105: 2266-2273.
42. Zimmerman JL, Shen MC,. Rhabdomyolysis. Chest 2013; 144: 1058-1065.
43. Almyroudis NG, Grimm MJ, Davidson BA, et al. NETosis and NADPH oxidase: at the intersection of host defense, inflammation, and injury. Front Immunol 2013; 4: 45.
44. Marcos V, Zhou Z, Yildirim AO, et al. CXCR2 mediates NADPH oxidase-independent neutrophil extracellular trap formation in cystic fibrosis airway inflammation. Nat Med 2010; 16: 1018-1023.
45. Chaudhary R, Katharia R,. Oxidative injury as contributory factor for red cells storage lesion during twenty eight days of storage. Blood Transfus 2012; 10: 59-62.