The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.
Viable neutrophils release mitochondrial DNA to form neutrophil extracellular traps
Abstract
Neutrophil extracellular traps (NETs) represent extracellular structures able to bind and kill microorganisms. It is believed that they are generated by neutrophils undergoing cell death, allowing these dying or dead cells to kill microbes. We show that, following priming with granulocyte/macrophage colony-stimulating factor (GM-CSF) and subsequent short-term toll-like receptor 4 (TLR4) or complement factor 5a (C5a) receptor stimulation, viable neutrophils are able to generate NETs. Strikingly, NETs formed by living cells contain mitochondrial, but no nuclear, DNA. Pharmacological or genetic approaches to block reactive oxygen species (ROS) production suggested that NET formation is ROS dependent. Moreover, neutrophil populations stimulated with GM-CSF and C5a showed increased survival compared with resting neutrophils, which did not generate NETs. In conclusion, mitochondrial DNA release by neutrophils and NET formation do not require neutrophil death and do also not limit the lifespan of these cells.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Different cellular lineages (10–18) may extrude their mitochondria upon activation.”
From Autoantibodies in Systemic Lupus Erythematosus Target Mitochondrial RNA (2019) · cites this paper as [10]
In the citing paper
“Various cellular lineages are capable of extruding their mitochondria. Activated mast cells10, T-cells11, eosinophils12, hepatocytes13, neutrophils14–16 and platelets17,18, in addition to damaged organs or tissues7,13,19,20, release extracellular mitochondria.”
From Anti-mitochondrial autoantibodies in systemic lupus erythematosus and their association with disease manifestations (2019) · cites this paper as [14]
In the citing paper
“during immune response, neutrophils utilize mtDNA as a structural molecule to bind cytotoxic proteins into neutrophil extracellular traps (NETs), which are then released onto advancing plaque biofilms (Yousefi et al., 2009)”
From Successful enrichment and recovery of whole mitochondrial genomes from ancient human dental calculus (2016) · cites this paper as Yousefi et al., 2009
In the citing paper
“Several reports demonstrate that a considerable fraction of the nucleic acids contained in NETs is of mitochondrial, rather than nuclear, origin [724–728].”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [724]
In the citing paper
“both NETotic cell death and NET extrusion in the absence of RCD appears to rely on the activity of NADPH oxidases [724, 736, 737].”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [724]
In the citing paper
“NET extrusion per se does not necessarily result in cellular lysis [722, 724, 735].”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [724]
Citations
Cites
Neutrophil Extracellular Traps Kill Bacteria
Brinkmann, V., Reichard, U., Goosmann, C., Fauler, B., Uhlemann, Y., Weiss, D. S., Weinrauch, Y., & Zychlinsky, A. (2004) · Science · doi:10.1126/science.1092385 · Cited by 10,268
Novel cell death program leads to neutrophil extracellular traps
Fuchs, T. A., Abed, U., Goosmann, C., Hurwitz, R., Schulze, I., Wahn, V., Weinrauch, Y., Brinkmann, V., & Zychlinsky, A. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200606027 · Cited by 3,197
Neutrophils and immunity: challenges and opportunities
Nathan, C. (2006) · Nature reviews. Immunology · doi:10.1038/nri1785 · Cited by 2,971
Platelet TLR4 activates neutrophil extracellular traps to ensnare bacteria in septic blood
Clark, S. R., Ma, A. C., Tavener, S. A., McDonald, B., Goodarzi, Z., Kelly, M. M., Patel, K. D., Chakrabarti, S., McAvoy, E., Sinclair, G. D., et al. (2007) · Nature Medicine · doi:10.1038/nm1565 · Cited by 2,309
Calpain-mediated cleavage of Atg5 switches autophagy to apoptosis
Yousefi, S., Perozzo, R., Schmid, I., Ziemiecki, A., Schaffner, T., Scapozza, L., Brunner, T., & Simon, H.-U. (2006) · Nature Cell Biology · doi:10.1038/ncb1482 · Cited by 1,158
Self-citationCatapult-like release of mitochondrial DNA by eosinophils contributes to antibacterial defense
Yousefi, S., Gold, J. A., Andina, N., Lee, J. J., Kelly, A. M., Kozlowski, E., Schmid, I., Straumann, A., Reichenbach, J., Gleich, G. J., et al. (2008) · Nature Medicine · doi:10.1038/nm.1855 · Cited by 967
Self-citationBeneficial suicide: why neutrophils die to make NETs
Brinkmann, V., & Zychlinsky, A. (2007) · Nature Reviews Microbiology · doi:10.1038/nrmicro1710 · Cited by 937
Selective fluorescent imaging of superoxide in vivo using ethidium-based probes
Robinson, K. M., Janes, M. S., Pehar, M., Monette, J. S., Ross, M. F., Hagen, T. M., Murphy, M. P., & Beckman, J. S. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601945103 · Cited by 777
von Köckritz‐Blickwede, M., Goldmann, O., Thulin, P., Heinemann, K., Norrby‐Teglund, A., Rohde, M., & Medina, E. (2008) · Blood · doi:10.1182/blood-2007-07-104018 · Cited by 566
Gupta, A. K., Hasler, P., Holzgreve, W., Gebhardt, G., & Hahn, S. (2005) · Human Immunology · doi:10.1016/j.humimm.2005.11.003 · Cited by 412
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 1,000
ATP amplifies NADPH-dependent and -independent neutrophil extracellular trap formation
Sofoluwe, A., Bacchetta, M., Badaoui, M., Kwak, B. R., & Chanson, M. (2019) · Scientific Reports · doi:10.1038/s41598-019-53058-9 · Cited by 68
The emerging role for metabolism in fueling neutrophilic inflammation
Morrison, T., Watts, E., Sadiku, P., & Walmsley, S. R. (2022) · Immunological Reviews · doi:10.1111/imr.13157 · Cited by 67
Lu, T., Kobayashi, S. D., Quinn, M. T., & DeLeo, F. R. (2012) · Frontiers in Immunology · doi:10.3389/fimmu.2012.00365 · Cited by 71
Histophilus somni causes extracellular trap formation by bovine neutrophils and macrophages
Hellenbrand, K. M., Forsythe, K. M., Rivera-Rivas, J. J., Czuprynski, C. J., & Aulik, N. A. (2012) · Microbial Pathogenesis · doi:10.1016/j.micpath.2012.09.007 · Cited by 70
Stawski, R. S., Walczak, K., Kosielski, P., Meissner, P., Budlewski, T., Padula, G., & Nowak, D. (2017) · PLoS ONE · doi:10.1371/journal.pone.0178216 · Cited by 67
Sources of Pathogenic Nucleic Acids in Systemic Lupus Erythematosus
Mustelin, T., Lood, C., & Giltiay, N. V. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01028 · Cited by 69
Neutrophil Extracellular Traps and Liver Disease
Hilscher, M. B., & Shah, V. H. (2019) · Seminars in Liver Disease · doi:10.1055/s-0039-3399562 · Cited by 66
G-CSF and GM-CSF Modify Neutrophil Functions at Concentrations found in Cystic Fibrosis
Castellani, S., D’Oria, S., Diana, A., Polizzi, A. M., Gioia, S. D., Mariggiò, M. A., Guerra, L., Favia, M., Vinella, A., Leonetti, G., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-49419-z · Cited by 65
Huang, S. U.-S., & O’Sullivan, K. M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23073793 · Cited by 72
Orchestration of Adaptive T Cell Responses by Neutrophil Granule Contents
Minns, D., Smith, K. J., & Findlay, E. G. (2019) · Mediators of Inflammation · doi:10.1155/2019/8968943 · Cited by 68
Recent progress in the mechanistic understanding of NET formation in neutrophils
Liu, M., Lyu, X., & Werth, V. P. (2021) · FEBS Journal · doi:10.1111/febs.16036 · Cited by 69
Targeting GM-CSF in inflammatory and autoimmune disorders
Achuthan, A. A., Lee, M.-C., & Hamilton, J. A. (2021) · Seminars in Immunology · doi:10.1016/j.smim.2021.101523 · Cited by 66
Chen, Y., Li, X., Lin, X., Liang, H., Liu, X., Zhang, X., Zhang, Q., Zhou, F., Chen, Y., Lei, L., et al. (2022) · Thrombosis Journal · doi:10.1186/s12959-022-00384-0 · Cited by 68
NETosis: an emerging therapeutic target in renal diseases
Juha, M., Molnár, A., Jakus, Z., & Ledó, N. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1253667 · Cited by 67
Neutrophils’ Contribution to Periodontitis and Periodontitis-Associated Cardiovascular Diseases
Bassani, B., Cucchiara, M., Butera, A., Kayali, O., Chiesa, A., Palano, M. T., Olmeo, F., Gallazzi, M., Dellavia, C. P. B., Mortara, L., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242015370 · Cited by 71
Guo, Y., Gao, F., Wang, Q., Wang, K., Pan, S., Pan, Z., Xu, S. S., Li, L., & Zhao, D. (2021) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2021.9784 · Cited by 68
Moonlighting chromatin: when DNA escapes nuclear control
Singh, J., Boettcher, M., Dölling, M., Heuer, A., Hohberger, B., Leppkes, M., Naschberger, E., Schapher, M., Schauer, C., Schoen, J., et al. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-023-01124-1 · Cited by 66
NETopathies? Unraveling the Dark Side of Old Diseases through Neutrophils
Mitsios, A., Αραμπατζιόγλου, Α., Arelaki, S., Mitroulis, I., & Ritis, K. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00678 · Cited by 68
On Neutrophil Extracellular Trap (NET) Removal: What We Know Thus Far and Why So Little
Santocki, M., & Kołaczkowska, E. (2020) · Cells · doi:10.3390/cells9092079 · Cited by 63
Neutrophil extracellular traps in central nervous system pathologies: A mini review
Shafqat, A., Eddin, A. N., Adi, G., Al-Rimawi, M., Rab, S. A., Abu-Shaar, M., Adi, K., AlKattan, K. M., & Yaqinuddin, A. (2023) · Frontiers in Medicine · doi:10.3389/fmed.2023.1083242 · Cited by 62
Konstantinov, Y. M., Dietrich, A., Weber‐Lotfi, F., Ibrahim, N., Клименко, Е. С., Тарасенко, В. И., Болотова, Т. А., & Koulintchenko, M. V. (2016) · Biochemistry (Moscow) · doi:10.1134/s0006297916100035 · Cited by 380
NETosis as a Pathogenic Factor for Heart Failure
Ling, S., & Xu, J. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/6687096 · Cited by 64
The role of neutrophils in alcohol-related hepatitis
Khan, R. S., Lalor, P. F., Thursz, M. R., & Newsome, P. N. (2023) · Journal of Hepatology · doi:10.1016/j.jhep.2023.05.017 · Cited by 63
A Narrative Review: The Role of NETs in Acute Respiratory Distress Syndrome/Acute Lung Injury
Zhou, X., Jin, J., Lv, T., & Song, Y. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25031464 · Cited by 62
Cell necrosis–independent sustained mitochondrial and nuclear DNA release following trauma surgery
McIlroy, D. J., Bigland, M. J., White, A. E., Hardy, B. M., Lott, N. J., Smith, D. W., & Balogh, Z. J. (2015) · The Journal of Trauma: Injury, Infection, and Critical Care · doi:10.1097/ta.0000000000000519 · Cited by 62
Morales-Primo, A. U., Becker, I., & Zamora‐Chimal, J. (2021) · International Reviews of Immunology · doi:10.1080/08830185.2021.1921174 · Cited by 64
Emerging role of neutrophil extracellular traps in the complications of diabetes mellitus
Shafqat, A., Rab, S. A., Ammar, O., Alsalameh, S., Alkhudairi, A., Kashir, J., AlKattan, K. M., & Yaqinuddin, A. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.995993 · Cited by 62
Gao, F., Peng, H., Gou, R., Zhou, Y., Ren, S., & Li, F. (2025) · Experimental Hematology and Oncology · doi:10.1186/s40164-025-00670-3 · Cited by 68
Immunometabolism in systemic lupus erythematosus
Patiño‐Martínez, E., & Kaplan, M. J. (2025) · Nature Reviews Rheumatology · doi:10.1038/s41584-025-01267-0 · Cited by 72
The Immune System Throws Its Traps: Cells and Their Extracellular Traps in Disease and Protection
Conceição‐Silva, F., Reis, C. S. M., Luca, P. M. D., Leite-Silva, J., Santiago, M. A., Morrot, A., & Morgado, F. N. (2021) · Cells · doi:10.3390/cells10081891 · Cited by 63
Autoantibodies in Systemic Lupus Erythematosus Target Mitochondrial RNA
Becker, Y., Marcoux, G., Allaeys, I., Julien, A.-S., Loignon, R.-C., Benk-Fortin, H., Rollet-Labelle, E., Rauch, J., Fortin, P. R., & Boilard, E. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01026 · Cited by 59
Stojkov, D., Gigon, L., Peng, S., Łukowski, R., Ruth, P., Karaulov, A. V., Rizvanov, A. A., Barlev, N. A., Yousefi, S., & Simon, H. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.826515 · Cited by 63
Self-citationROS fine-tunes the function and fate of immune cells
Liu, S., Huang, B., Cao, J., Wang, Y., Xiao, H., Zhu, Y., & Zhang, H. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110069 · Cited by 62
From neutrophil extracellular traps release to thrombosis: an overshooting host‐defense mechanism?
Borissoff, J. I., & Cate, H. T. (2011) · Journal of Thrombosis and Haemostasis · doi:10.1111/j.1538-7836.2011.04425.x · Cited by 62
Visualization and Functional Evaluation of Phagocyte Extracellular Traps
von Köckritz‐Blickwede, M., Chow, O. A., Ghochani, M., & Nizet, V. (2010) · Methods in microbiology · doi:10.1016/s0580-9517(10)37007-3 · Cited by 59
Neutrophil Extracellular Traps in Autoimmune Diseases
He, Y., Yang, F., & Sun, E. (2018) · Chinese Medical Journal · doi:10.4103/0366-6999.235122 · Cited by 59
Role of Neutrophil Extracellular Traps in Asthma and Chronic Obstructive Pulmonary Disease
Liu, T., Wang, F., Wang, G., & Mao, H. Z. (2017) · Chinese Medical Journal · doi:10.4103/0366-6999.201608 · Cited by 58
Mechanisms and disease relevance of neutrophil extracellular trap formation
Avondt, K. V., & Hartl, D. (2018) · European Journal of Clinical Investigation · doi:10.1111/eci.12919 · Cited by 60
Díaz-Godínez, C., Fonseca, Z., Néquiz, M., Laclette, J. P., Rosales, C., & Carrero, J. C. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00184 · Cited by 59
Therapeutic Targeting of Neutrophil Granulocytes in Inflammatory Liver Disease
Bartneck, M., & Wang, J. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02257 · Cited by 58
Pulp Innate Immune Defense: Translational Opportunities
Duncan, H. F., & Cooper, P. R. (2020) · Journal of Endodontics · doi:10.1016/j.joen.2020.06.019 · Cited by 57
Hippo/YAP signaling pathway protects against neomycin-induced hair cell damage in the mouse cochlea
Wang, M., Dong, Y., Gao, S., Zhong, Z., Cheng, C., Qiang, R., Zhang, Y., Shi, X., Qian, X., Gao, X., et al. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-04029-9 · Cited by 58
Neutrophil extracellular trap: A key player in the pathogenesis of autoimmune diseases
Sadeghi, M., Dehnavi, S., Jamialahmadi, T., Johnston, T. P., & Sahebkar, A. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.109843 · Cited by 59
Neutrophil dysfunction in bronchiectasis: an emerging role for immunometabolism
Giam, Y. H., Shoemark, A., & Chalmers, J. D. (2021) · European Respiratory Journal · doi:10.1183/13993003.03157-2020 · Cited by 58
Neutrophils in host defense, healing, and hypersensitivity: Dynamic cells within a dynamic host
Siwicki, M. R., & Kubes, P. (2023) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2022.12.004 · Cited by 59
Wang, C. J., Ko, G. R., Lee, Y. Y., Park, J., Park, W., Park, T., Jin, Y., Kim, S.-N., Lee, J. S., & Park, C. G. (2024) · Nano Convergence · doi:10.1186/s40580-024-00414-9 · Cited by 61
Bmi1 regulates auditory hair cell survival by maintaining redox balance
Chen, Y., Li, H., Ni, W., Zhang, Y., Sun, S., Miao, D., Chai, R., & Li, H. (2015) · Cell Death and Disease · doi:10.1038/cddis.2014.549 · Cited by 54
Does NETosis Contribute to the Bacterial Pathoadaptation in Cystic Fibrosis?
Rahman, S., & Gadjeva, M. G. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00378 · Cited by 56
Mechanisms of toxicity mediated by neutrophil and eosinophil granule proteins
Gigon, L., Yousefi, S., Karaulov, A. V., & Simon, H. (2020) · Allergology International · doi:10.1016/j.alit.2020.11.003 · Cited by 58
Self-citationNETosis in Wound Healing: When Enough Is Enough
Sabbatini, M., Magnelli, V., & Renò, F. (2021) · Cells · doi:10.3390/cells10030494 · Cited by 61
Neutrophil Extracellular Traps: New Aspects
Vorobjeva, N. V. (2020) · Moscow University Biological Sciences Bulletin · doi:10.3103/s0096392520040112 · Cited by 57
NET formation is independent of gasdermin D and pyroptotic cell death
Stojkov, D., Claus, M., Kozlowski, E., Oberson, K., Schären, O. P., Benarafa, C., Yousefi, S., & Simon, H. (2023) · Science Signaling · doi:10.1126/scisignal.abm0517 · Cited by 60
Self-citationAutophagy regulation in macrophages and neutrophils
Mihalache, C. C., & Simon, H. (2012) · Experimental Cell Research · doi:10.1016/j.yexcr.2011.12.021 · Cited by 55
Self-citationMuñoz-Caro, T., Conejeros, I., Zhou, E., Pikhovych, A., Gärtner, U., Hermosilla, C. R., Kulke, D., & Taubert, A. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00968 · Cited by 55
Therapeutic Targeting of Neutrophil Extracellular Traps in Atherogenic Inflammation
Avondt, K. V., Mäegdefessel, L., & Soehnlein, O. (2019) · Thrombosis and Haemostasis · doi:10.1055/s-0039-1678664 · Cited by 56
The involvement of NETs in ANCA-associated vasculitis
Shiratori‐Aso, S., & Nakazawa, D. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1261151 · Cited by 59
The impact of aging on neutrophil functions and the contribution to periodontitis
Wang, Z., Saxena, A., Yan, W., Uriarte, S. M., de Siqueira, R. A. C., & Li, X. (2025) · International Journal of Oral Science · doi:10.1038/s41368-024-00332-w · Cited by 65
Silva, L. M. R., Muñoz-Caro, T., Burgos, R. A., Hidalgo, M. A., Taubert, A., & Hermosilla, C. R. (2016) · Mediators of Inflammation · doi:10.1155/2016/5898074 · Cited by 54
Ma, F., Chang, X., Wang, G., Zhou, H., Ma, Z., Lin, H., & Fan, H. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02854 · Cited by 53
Peripheral Blood Mononuclear Cells Demonstrate Mitochondrial Damage Clearance During Sepsis
Kraft, B. D., Chen, L., Suliman, H. B., Piantadosi, C. A., & Welty‐Wolf, K. E. (2019) · Critical Care Medicine · doi:10.1097/ccm.0000000000003681 · Cited by 55
Diverse Neutrophil Functions in Cancer and Promising Neutrophil-Based Cancer Therapies
Sounbuli, K., Mironova, N. L., & Alekseeva, L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232415827 · Cited by 54
Neutrophils: game changers in glomerulonephritis?
Mayadas, T. N., Rosetti, F., Ernandez, T., & Sethi, S. M. (2010) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2010.06.002 · Cited by 53
Mitochondrial DNA in cell death and inflammation
Heilig, R., Lee, J., & Tait, S. W. G. (2023) · Biochemical Society Transactions · doi:10.1042/bst20221525 · Cited by 56
Colicchia, M., Perrella, G., Gant, P., & Rayes, J. (2023) · Research and Practice in Thrombosis and Haemostasis · doi:10.1016/j.rpth.2023.100116 · Cited by 58
Relevance of Macrophage Extracellular Traps in C. albicans Killing
Loureiro, A., Pais, C., & Sampaio, P. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02767 · Cited by 52
Neutrophil extracellular traps: New players in cancer research
Zhao, J., & Jin, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.937565 · Cited by 54
Torp, M., Vaage, J., & Stensløkken, K. (2023) · Acta Physiologica · doi:10.1111/apha.13920 · Cited by 54
Melbouci, D., Ahmad, A. H., & Decker, P. (2023) · RMD Open · doi:10.1136/rmdopen-2023-003104 · Cited by 54
Neutrophils and neutrophil extracellular traps in oral health and disease
Kim, T. S., & Moutsopoulos, N. M. (2024) · Experimental & Molecular Medicine · doi:10.1038/s12276-024-01219-w · Cited by 59
Extracellular Traps: An Ancient Weapon of Multiple Kingdoms
Neumann, A., Brogden, G., & von Köckritz‐Blickwede, M. (2020) · Biology · doi:10.3390/biology9020034 · Cited by 54
Damage associated molecular patterns and neutrophil extracellular traps in acute pancreatitis
Zhou, X., Jin, S., Pan, J., Lin, Q., Yang, S., Ambe, P. C., Basharat, Z., Zimmer, V., Wang, W., & Hong, W. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.927193 · Cited by 51
Zhao, H., Liang, Y., Sun, C., Zhai, Y., Li, X., Jiang, M., Yang, R., Li, X., Shu, Q., Kai, G., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232315180 · Cited by 50
Mycobacterium massiliense Induces Macrophage Extracellular Traps with Facilitating Bacterial Growth
Je, S., Quan, H., Yoon, Y., Na, Y., Kim, B., & Seok, S. H. (2016) · PLoS ONE · doi:10.1371/journal.pone.0155685 · Cited by 49
Neutrophil Extracellular Traps in the Establishment and Progression of Renal Diseases
Salazar-González, H., Zepeda-Hernandez, A., Melo, Z., Saavedra-Mayorga, D. E., & Echavarría, R. (2019) · Medicina · doi:10.3390/medicina55080431 · Cited by 52
Neutrophil Extracellular Traps in Candida albicans Infection
He, Y., Liu, J., Chen, Y., Yan, L., & Wu, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.913028 · Cited by 50
Pisareva, E., Mihalovičová, L., Pastor, B., Kudriavtsev, A., Mirandola, A., Mazard, T., Badiou, S., Maus, U. A., Ostermann, L., Weinmann‐Menke, J., et al. (2022) · Genome Medicine · doi:10.1186/s13073-022-01125-8 · Cited by 48
Expanding Neutrophil Horizons: New Concepts in Inflammation
Chatfield, S. M., Thiéblemont, N., & Witko‐Sarsat, V. (2018) · Journal of Innate Immunity · doi:10.1159/000493101 · Cited by 52
Extracellular Trap by Blood Cells: Clinical Implications
Nija, R. J., Sanju, S., Sidharthan, N., & Mony, U. (2020) · Tissue Engineering and Regenerative Medicine · doi:10.1007/s13770-020-00241-z · Cited by 50
Kratochvil, M. J., Kaber, G., Demirdjian, S., Cai, P. C., Burgener, E. B., Nagy, N., Barlow, G. L., Popescu, M. C., Nicolls, M. R., Ozawa, M. G., et al. (2022) · JCI Insight · doi:10.1172/jci.insight.152629 · Cited by 46
Sekheri, M., Othman, A., & Filep, J. G. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.660760 · Cited by 51
Singh, B., Modica-Napolitano, J. S., & Singh, K. K. (2017) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2017.05.004 · Cited by 49
NET Formation in Bullous Pemphigoid Patients With Relapse Is Modulated by IL-17 and IL-23 Interplay
Giusti, D., Bini, E. I., Terryn, C., Didier, K., Jan, S. L., Gatouillat, G., Durlach, A., Nesmond, S., Muller, C. B., Bernard, P., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00701 · Cited by 48
Chen, X., Li, Y., Qin, L., He, R., & Hu, C. (2020) · Immunological Investigations · doi:10.1080/08820139.2020.1778720 · Cited by 48
Phagocytosis and neutrophil extracellular traps
DeLeo, F. R., & Allen, L. H. (2020) · Faculty Reviews · doi:10.12703/r/9-25 · Cited by 53
Neumann, A., Brogden, G., Jerjomiceva, N., Brodesser, S., Naim, H. Y., & von Köckritz‐Blickwede, M. (2014) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2014.07.005 · Cited by 47
Neutrophil extracellular traps in bacterial infections: Strategies for escaping from killing
Araźna, M., Pruchniak, M. P., & Demkow, U. A. (2013) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2013.03.002 · Cited by 47
Uddin, M., Lau, L. C., Seumois, G., Vijayanand, P., Staples, K. J., Bagmane, D., Cornelius, V. R., Dorinsky, P., Davies, D. E., & Djukanović, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0072502 · Cited by 47
Understanding the molecular mechanisms of NETs and their role in antiviral innate immunity
Agraz‐Cibrián, J. M., Giraldo, D. M., Mary, F.-M., & Inchima, S. U. (2016) · Virus Research · doi:10.1016/j.virusres.2016.11.033 · Cited by 50
Hyperoxidation of ether-linked phospholipids accelerates neutrophil extracellular trap formation
Yotsumoto, S., Muroi, Y., Chiba, T., Ohmura, R., Yoneyama, M., Magarisawa, M., Dodo, K., Terayama, N., Sodeoka, M., Aoyagi, R., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-15668-z · Cited by 47
Mitochondrial DNA and Exercise: Implications for Health and Injuries in Sports
Zanini, G., De Gaetano, A., Selleri, V., Savino, G., Cossarizza, A., Pinti, M., Mattioli, A. V., & Nasi, M. (2021) · Cells · doi:10.3390/cells10102575 · Cited by 46
Neutrophil extracellular traps in tumor progression and immunotherapy
Yan, M., Gu, Y., Sun, H., & Ge, Q. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1135086 · Cited by 48
Schneider, A. E., Sándor, N., Kárpáti, É., & Józsi, M. (2016) · Molecular Immunology · doi:10.1016/j.molimm.2016.02.011 · Cited by 45
Neutrophil Extracellular Traps in Respiratory Disease: guided anti-microbial traps or toxic webs?
Cortjens, B., van Woensel, J. B. M., & Reinout, A. (2016) · Paediatric Respiratory Reviews · doi:10.1016/j.prrv.2016.03.007 · Cited by 50
von Köckritz‐Blickwede, M., & Winstel, V. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.836278 · Cited by 46
The emerging role of neutrophilic extracellular traps in intestinal disease
Chen, F., Liu, Y., Shi, Y., Zhang, J., Liu, X., Liu, Z., Lv, J., & Leng, Y. (2022) · Gut Pathogens · doi:10.1186/s13099-022-00497-x · Cited by 48
The emerging role of neutrophil extracellular traps in fungal infection
Liang, C.-T., Lian, N., & Li, M. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.900895 · Cited by 48
Clinical significance of neutrophil extracellular traps biomarkers in thrombosis
Xu, X., Wu, Y., Xu, S., Yin, Y., Ageno, W., Stefano, V. D., Zhao, Q., & Qi, X. (2022) · Thrombosis Journal · doi:10.1186/s12959-022-00421-y · Cited by 52
Sudakov, N. P., Апарцин, К. А., Lepekhova, S. A., Nikiforov, S. B., Katyshev, A. I., Израйлевна, Л. Г., Vybivantseva, A. V., & Konstantinov, Y. M. (2017) · European journal of medical research · doi:10.1186/s40001-016-0241-x · Cited by 45
Wang, Y., Guo, Y., Wen, P., Zhao, Z., Xie, J., Yang, K. C., Yang, Q., Wang, J.-F., & Deng, X. (2020) · Mediators of Inflammation · doi:10.1155/2020/2720369 · Cited by 45
Sanchez‐Pino, M. D., Richardson, W. S., Zabaleta, J., Puttalingaiah, R. T., Chapple, A. G., Liu, J., Kim, Y., Ponder, M. M., DeArmitt, R., Baiamonte, L. B., et al. (2022) · EBioMedicine · doi:10.1016/j.ebiom.2022.103910 · Cited by 44
Metadata
- Authors
- Yousefi, S., Mihalache, C., Kozlowski, E., Schmid, I., & Simon, H. U.
- Affiliations
- University of Bern (CH)
- Corresponding author
- Yousefi, S
- ORCID
- Venue
- Cell Death & Differentiation
- Published
- 2009-07-17
- Volume
- 16
- Issue
- 11
- Pages
- 1438-1444
- ISSN
- 1350-9047 (ISSN-L)
- 1476-5403
- OpenAlex
- W2056112680
- Cited by
- 1,036
- References
- 17
- Citations by year
- 2026: 84 · 2025: 82 · 2024: 67 · 2023: 89 · 2022: 92 · 2021: 93 · 2020: 84 · 2019: 79 · 2018: 66 · 2017: 57 · 2016: 66 · 2015: 43 · 2014: 28 · 2013: 36 · 2012: 36
- FWCI
- 9.90
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Cell Death and Differentiation (publishedVersion)
- PubMed (publishedVersion)
- Bern Open Repository and Information System (University of Bern) (submittedVersion)
- Funders
- National Science Foundation
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (107526, 112078)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Life Sciences › Immunology and Microbiology › Microbiology › Antimicrobial Peptides and Activities
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Keywords
- neutrophil extracellular traps, mitochondrial DNA release, neutrophil survival, reactive oxygen species, GM-CSF, TLR4, C5a receptor, innate immunity, antimicrobial defense
- MeSH terms
- DNA, Mitochondrial, Humans, Neutrophils, Complement C5a, Granulocyte-Macrophage Colony-Stimulating Factor, Apoptosis, Reactive Oxygen Species, Neutrophil Activation, Toll-Like Receptor 4
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review