The DOI matches its Crossref record; 51 of the 51 references it cites were found in a registry or an index.
Neutrophil extracellular trap cell death requires both autophagy and superoxide generation
Open accessAbstract
Neutrophil extracellular traps (NETs) are extracellular chromatin structures that can trap and degrade microbes. They arise from neutrophils that have activated a cell death program called NET cell death, or NETosis. Activation of NETosis has been shown to involve NADPH oxidase activity, disintegration of the nuclear envelope and most granule membranes, decondensation of nuclear chromatin and formation of NETs. We report that in phorbol myristate acetate (PMA)-stimulated neutrophils, intracellular chromatin decondensation and NET formation follow autophagy and superoxide production, both of which are required to mediate PMA-induced NETosis and occur independently of each other. Neutrophils from patients with chronic granulomatous disease, which lack NADPH oxidase activity, still exhibit PMA-induced autophagy. Conversely, PMA-induced NADPH oxidase activity is not affected by pharmacological inhibition of autophagy. Interestingly, inhibition of either autophagy or NADPH oxidase prevents intracellular chromatin decondensation, which is essential for NETosis and NET formation, and results in cell death characterized by hallmarks of apoptosis. These results indicate that apoptosis might function as a backup program for NETosis when autophagy or NADPH oxidase activity is prevented.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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
“NETotic cell death has been suggested to result from a signaling pathway that involves Raf-1 proto-oncogene, serine/threonine kinase (RAF1), mitogen-activated protein kinase kinases (MAP2Ks), and ERK2, culminating with NADPH oxidase activation and consequent ROS generation [736, 738, 739].”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [739]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
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
Autophagy in the Pathogenesis of Disease
Levine, B., & Kroemer, G. (2008) · Cell · doi:10.1016/j.cell.2007.12.018 · Cited by 7,069
Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009
Kroemer, G., Galluzzi, L., Vandenabeele, P., Abrams, J., Alnemri, E. S., Baehrecke, E. H., Blagosklonny, M. V., El-Deiry, W. S., Golstein, P., Green, D. R., et al. (2009) · Cell Death & Differentiation · doi:10.1038/cdd.2008.150 · Cited by 3,399
Self-citationNovel 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
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
BABIOR, B. M. (1999) · Blood · doi:10.1182/blood.v93.5.1464 · Cited by 2,147
Reactive oxygen species are essential for autophagy and specifically regulate the activity of Atg4
Scherz‐Shouval, R., Shvets, E., Fass, E., Shorer, H., Gil, L., & Elazar, Z. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601623 · Cited by 2,101
Identification of RIP1 kinase as a specific cellular target of necrostatins
Degterev, A., Hitomi, J., Germscheid, M., Ch'en, I. L., Korkina, O., Teng, X., Abbott, D., Cuny, G. D., Yuan, C., Wagner, G., et al. (2008) · Nature Chemical Biology · doi:10.1038/nchembio.83 · Cited by 2,059
Netting neutrophils in autoimmune small-vessel vasculitis
Kessenbrock, K., Krumbholz, M., Schönermarck, U., Back, W. E., Gross, W. L., Werb, Z., Gröne, H., Brinkmann, V., & Jenne, D. E. (2009) · Nature Medicine · doi:10.1038/nm.1959 · Cited by 1,687
Inhibition of Macroautophagy Triggers Apoptosis
Boya, P., González‐Polo, R. A., Casares, N., Perfettini, J., Dessen, P., Larochette, N., Métivier, D., Meley, D., Souquère, S., Yoshimori, T., et al. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.3.1025-1040.2005 · Cited by 1,669
Flagged first, then by citations
Cited by
Sorted by citations
Items 701–800 of 818
Dai, H., Zheng, Y., Li, C., Yang, B., Huang, Q., Ran, X., Ke, S., & Li, Y. (2026) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2026.05.287 · Cited by 1
Autophagy, NET formation, and inflammation crosstalk in thrombotic autoimmune diseases
Muralt, T., Buonomo, S. M., Tschan, M. P., & Schaller, M. M. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1844170 · Cited by 1
Zhang, X., Dallenga, T. K., & Krauss‐Etschmann, S. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1919974 · Cited by 1
Woo, S. (2012) · Journal of Bacteriology and Virology · doi:10.4167/jbv.2012.42.2.172 · Cited by 1
Generation of Unfolded DNA in Human Neutrophils Following Hypothermal Treatment
Kawata, J., Kikuchi, M., & Saitoh, H. (2013) · CellBio · doi:10.4236/cellbio.2013.23013 · Cited by 1
Basyreva, L. Y. (2014) · Immunome Research · doi:10.4172/1745-7580.1000065 · Cited by 1
Neutrophils in Acute Bacterial Pneumonia
Gomez, J. C., Wang, Q., & Doerschuk, C. M. (2012) · Springer eBooks · doi:10.1007/978-1-4614-5326-0_4 · Cited by 1
Dynamic regulation of neutrophil activation, migration and death
Itakura, A. (2013) · doi:10.6083/m43t9f7z · Cited by 1
Chronic Granulomatous Disease and Aspergillosis
Grimm, M. J., & Segal, B. H. (2017) · Springer eBooks · doi:10.1007/978-3-319-50842-9_4 · Cited by 1
The Impact of Age on Neutrophil Extracellular Trap Formation
Hazeldine, J., & Lord, J. M. (2019) · Springer eBooks · doi:10.1007/978-3-319-99375-1_102 · Cited by 1
Mitoxantrone Inhibits FMLP-Induced Degenerative Changes in Human Neutrophils
Ali, S., Shehwar, D., & Alam, M. R. (2021) · Molecular Biology · doi:10.1134/s0026893321040026 · Cited by 1
Role of Nitric Oxide Synthase and Nitric Oxide Signaling in the Neutrophil Ontogeny and Functions
Kumar, S., Sadaf, S., & Dikshit, M. (2023) · Advances in biochemistry in health and disease · doi:10.1007/978-3-031-24778-1_8 · Cited by 2
Raudszus, L., Bahreini, F., Allan, S., Kalies, K., Caldwell, C. C., & Kalies, K. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1494400 · Cited by 1
Iba, T., Murai, M., Nagaoka, I., & Tabe, Y. (2013) · Nihon Kyukyu Igakukai Zasshi Journal of Japanese Association for Acute Medicine · doi:10.3893/jjaam.24.827 · Cited by 1
FUNCTIONAL ACTIVITY OF NEUTROPHILS IN CHRONIC RECURRENT FURUNCULOSIS
Новикова, И. А., Гусакова, Н. В., & Hamaliaka, A. (2014) · Medical Immunology (Russia) · doi:10.15789/1563-0625-2014-1-81-88 · Cited by 1
Eosinophil extracellular traps: mechanisms of formation, functions
Minina, E., & Novikov, P. (2019) · Immunopathology Allergology Infectology · doi:10.14427/jipai.2019.2.38 · Cited by 1
Formación de trampas extracelulares de neutrófilos humanos In vitro: descripción de un método
Perez‐Zapata, L. J., Ramírez, A. M. T., Arias, A. A., & Quintero, J. Á. L. (2020) · Hechos Microbiológicos · doi:10.17533/udea.hm.v10n1a01 · Cited by 1
Neutrophil extracellular trap formation: an introduction
Rai, G. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-816147-0.00001-0 · Cited by 1
Cheng, L. (2015) · TSpace (University of Toronto) · Cited by 1
Dinsdale, R. J. (2017) · University of Birmingham Institutional Research Archive (University of Birmingham) · Cited by 1
BCG induced neutrophil extracellular traps formation and its regulatory mechanismPreprint
Sun, E., Liu, K., Lei, M., Wang, L., Nian, X., Li, L., & Gao, J. (2020) · doi:10.21203/rs.2.15638/v2 · Cited by 1
Ma, Y., Li, L., Hu, Y., Han, S., Yang, Q., Pu, W., Zhang, X., & Zhang, J. (2021) · Research Square · doi:10.21203/rs.3.rs-200054/v1 · Cited by 1
Antiphospholipid Antibodies and Syndrome
Cervera, R. (2018) · MDPI eBooks · doi:10.3390/books978-3-03842-948-7 · Cited by 3
Uremic Serum Damages Endothelium by Provoking Excessive Neutrophil Extracellular Trap FormationPreprint
Lee, H. W., Nizet, V., An, J. N., Lee, H., Song, Y. R., Kim, S. G., & Kim, J.-K. (2021) · Research Square · doi:10.21203/rs.3.rs-668603/v1 · Cited by 1
Li, T., Qian, Y., Li, H., Wang, T., Jiang, Q., Wang, Y., Zhu, Y., Li, S., He, X., Shi, G., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-3845429/v1 · Cited by 1
Lovell, C. D., Sierra, I., Welter, E. M., Sandoval-Heglund, D., Li, N., Vanderbeck, A., Lengner, C. J., Lepper, C., & Anguera, M. C. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.30.673230 · Cited by 1
Allen, J. P. (2011) · Human Biology
Kalra, S. (2014) · University of Birmingham Institutional Research Archive (University of Birmingham)
Mechanisms underlying innate immunesenescence
Hazeldine, J. (2013) · University of Birmingham Institutional Research Archive (University of Birmingham)
The Effect of Intravenous Immunoglobulin (IVIG) on Fibrosarcoma Growth in CBA and C57BL/6 Mice
Basyreva, L. Y. (2014) · Immunome Research · doi:10.4172/1745-7580.1000070
Neutrophils versus Pathogenic Fungi : through the magnifying glass of nutritional immunity
Niemiec, M. J. (2015) · DiVA at Umeå University (Umeå University)
Signal Inhibitory Receptor on Leukocytes-1 (SIRL-1), a potent regulator of neutrophil function
Avondt, K. V. (2014) · Utrecht University Repository (Utrecht University)
Funchal, G. A. (2014) · Americanae (AECID Library)
NOVEL BARRIERS TO THROMBOLYSIS: THE ROLE OF MECHANICAL STRESS AND NEUTROPHIL EXTRACELLULAR TRAPS
Varjú, I. (2015) · Semmelweis University Repository (Semmelweis University) · doi:10.14753/se.2015.1738
Neutrophil-Mediated Vascular Host Defense
Kim, J. H., & Yipp, B. G. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-801078-5.00002-9 · Cited by 1
Modulation of neutrophil extracellular trap formation in health and disease
Hosseinzadeh, A. (2015) · KTH Publication Database DiVA (KTH Royal Institute of Technology)
Sequential priming of neutrophils
Yao, Y. (2014) · OhioLink ETD Center (Ohio Library and Information Network)
Domingo-Gonzalez, R. (2014) · Deep Blue (University of Michigan)
The role of neutrophil extracellular traps (NETs) on infectious diseases
Hamaguchi, S., & TOMONO, K. (2016) · Japanese Journal of Thrombosis and Hemostasis · doi:10.2491/jjsth.27.34
Juneau, R. A. (2011) · WakeSpace Scholarship (Wake Forest University)
Su, D. (2016) · University of Liverpool · doi:10.17638/02029279
Transcriptional response of Mycobacterium tuberculosis on encounter with neutrophil in vitro
Bakir, A. (2016) · Leicester Research Archive (University of Leicester)
Nanofeatures of Biomaterials and their Impact on the Inflammatory Response
Pujari‐Palmer, S. (2016) · KTH Publication Database DiVA (KTH Royal Institute of Technology)
Autophagy in Chronic Inflammation
Arnold, J., Murera, D., & Gros, F. (2016) · Springer eBooks · doi:10.1007/978-3-319-30079-5_6
Necrobiology of Liver Cancer: Autophagy and Cellular Senescence
Zimmermann, A. (2016) · Springer eBooks · doi:10.1007/978-3-319-26587-2_179-1
Pathogenic Role of Autophagy in Rheumatic Diseases
Choi, Y. J., & Yoo, W. (2016) · Journal of Rheumatic Diseases · doi:10.4078/jrd.2016.23.4.202
Beneficial and Deleterious Effects of Neutrophil Extracellular Traps on Infection
Moreno-Altamirano, M. B., Cruz-Gómez, C. E., & López-Luis, L. E. (2017) · InTech eBooks · doi:10.5772/intechopen.68634
Vitamin C: A potential regulator of inflammatory response
Mohammed, B. M. (2015) · VCU Scholars Compass (Virginia Commonwealth University) · doi:10.25772/0kbv-0h96
Autophagy Regulates Inflammatory Responses in Antigen-Presenting Cells
Harris, J., Lang, T., & Sukkar, M. B. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-812146-7.00015-9
Armstrong, C. L. (2017) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/2769
Perioperative neutrophil immune function
Cain, D. J. (2017) · UCL Discovery (University College London)
The Effects of Mechanical Ventilation on Neutrophil Extracellular Trap Formation
Yildiz, C. (2013) · TSpace (University of Toronto)
Pijanowski, Ł., Homa, J., & Chadzińska, M. (2017) · Jagiellonian University Repository (Jagiellonian University)
Rai, G. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-816147-0.00003-4 · Cited by 1
Yuzeir, S., & Gercheva, L. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.93651
Group AStreptococcus-Mediated Host Cell Signaling
Pancholi, V. (2019) · ASM Press eBooks · doi:10.1128/9781683670131.ch9
Type-4 phosphodiesterase (PDE4) blockade prevents NETosis in cystic fibrosisPreprint
Totani, L., Amore, C., Piccoli, A. L., Jr., Dell’Elba, G., Santo, A. D., Plebani, R., Pecce, R., Martelli, N., Fino, I. D., Ranucci, S., et al. (2021) · doi:10.22541/au.161700109.94909942/v1
Elucidating the Role of Histone Acetylation in Regulating Neutrophil Extracellular Trap Formation
Hamam, H. J. (2019) · TSpace (University of Toronto)
The role of apoptosis during inflammation resolution in Lyme arthritis
Hilliard, K. A. (2019) · MOspace Institutional Repository (University of Missouri) · doi:10.32469/10355/75021
Intracellular Radicals in Neutrophils Processing and Functional Implications
Björnsdóttir, H. (2015) · Gothenburg University Publications Electronic Archive (Gothenburg University)
Ikegame, A., Kondo, A., Kitaguchi, K., Sasa, K., & Miyoshi, M. (2022) · Research Square · doi:10.21203/rs.3.rs-1346142/v1
Sapey, E. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.732544720.793558959
Sapey, E. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.731190977.793558956
Neutrophil Extracellular Traps
Marin‐Esteban, V., Barrientos, L., & Chollet‐Martin, S. (2013) · Encyclopedia of Inflammatory Diseases · doi:10.1007/978-3-0348-0620-6_181-1
Парамонова, Н. С., & Малолетникова, И. М. (2020) · Педиатрия Восточная Европа · doi:10.34883/pi.2020.8.2.002
BCG induced neutrophil extracellular traps formation and its regulatory mechanismPreprint
Sun, E., Liu, K., Lei, M., Wang, L., Nian, X., Li, L., & Gao, J. (2019) · doi:10.21203/rs.2.15638/v1
Necrobiology of Liver Cancer: Autophagy and Cellular Senescence
Zimmermann, A. (2016) · Springer eBooks · doi:10.1007/978-3-319-26956-6_179
Lionakis, M. S. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.727458344.793572027
BCG-induced neutrophil extracellular traps formation and its regulatory mechanismPreprint
Sun, E., Liu, K., Lei, M., Wang, L., Nian, X., Li, L., & Gao, J. (2020) · doi:10.21203/rs.2.15638/v3
Neutrophil extracellular traps in autoimmunity, renal diseases, and transplantation
Vega-Roman, C., Melo, Z., & Echavarría, R. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-85389-7.00021-1
Hyper-coagulopathy State in COVID-19: A Pivotal Challenge
Fard, N. N. G., Vaghf, A., Torfi, E., Shahrabi, S., & Pezeshki, S. M. S. (2023) · Current Respiratory Medicine Reviews · doi:10.2174/1573398x19666230703094330
Sphingosine and Other Amine-Containing Compounds Induce Rapid NOX-Independent NETosis
Voitenok, A. A., Lotosh, N. Y., Kulikov, E. A., Rogov, A. G., Vasilov, R. G., & Селищева, А. А. (2023) · Nanobiotechnology Reports · doi:10.1134/s2635167623601080
Secretagogin deficiency causes abnormal extracellular trap formation in microglia
Kim, Y. G., & Kim, D. (2024) · International Journal of Oral Biology · doi:10.11620/ijob.2024.49.2.34
Therapy of Allergic Rhinitis Using Ribavirin Spray to Clear Nasal Commensal VirusesPreprint
Dong, Y., Wang, T., Fan, Y., Zhou, Y., Li, Z., Qin, Y., Wang, Z., Liu, Y., Liu, S., Liang, C., et al. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.5005077
The pathophysiology of sepsis and autophagy
Watanabe, E., & Honda, G. (2024) · Japanese Journal of Thrombosis and Hemostasis · doi:10.2491/jjsth.35.702
Gao, Y., Hui, L., Dou, G., Chang, X., Tang, Y., Liu, H., Xu, Z., & Xu, B. (2025) · Brazilian Journal of Medical and Biological Research · doi:10.1590/1414-431x2024e13639
Aging changes the underlying mechanism of JAK2 modulation in neutrophil functionPreprint
Feldmann, J. W., Kays, M., McGinnis, F., Herron, E., Sati, N., Woods, C., & Coulibaly, A. P. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.21.649782
Cell Death Mechanisms, Associated Toxicity and Therapeutic Applications
Davila, J. C., Kovalova, N., & Radi, Z. A. (2025) · Elsevier eBooks · doi:10.1016/b978-0-323-95488-4.00265-5
Animal toxins and NETosis: A new frontier in innate immune modulation
de Oliveira, I. S., Ferreira, I. G., Jacob, B. D. C. D. S., Ramos, E., Agati, L., Vieira, B., Melo-dos-Santos, G., Magalhães, A., & Pucca, M. B. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.115758
Aging changes the mechanism that underlies JAK2 modulation of neutrophil function
Feldmann, J. W., Kays, M., McGinnis, F., Herron, E., Sati, N., Woods, C., & Coulibaly, A. P. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkaf323
Li, T., Qian, Y., Li, H., Wang, T., Jiang, Q., Wang, Y., Zhu, Y., Li, S., He, X., Shi, G., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25844531
Schroeder-Castagno, M., Serrato, A. D. R., Wilhelm, A., Romero‐Suárez, S., Schindler, P., Álvarez-González, C., Duchow, A.-S., Bellmann–Strobl, J., Ruprecht, K., Hastermann, M., et al. (2022) · Figshare · doi:10.6084/m9.figshare.21258302
Li, T., Qian, Y., Li, H., Wang, T., Jiang, Q., Wang, Y., Zhu, Y., Li, S., He, X., Shi, G., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25844429
Schroeder-Castagno, M., Serrato, A. D. R., Wilhelm, A., Romero‐Suárez, S., Schindler, P., Álvarez-González, C., Duchow, A.-S., Bellmann–Strobl, J., Ruprecht, K., Hastermann, M., et al. (2022) · Figshare · doi:10.6084/m9.figshare.21258299
Cuppen, J. J. M., & Savelkoul, H. F. J. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms27010143 · Cited by 1
Neutrophil S100a9 Deficiency Protects against Periodontal Bone Loss
Wei, Y. Y., Zheng, J. Q., Zhou, Y. L., Wu, H. L., Liu, X. Z., Yang, H. Y., Song, F. F., & Huang, C. (2026) · Journal of Dental Research · doi:10.1177/00220345251413516 · Cited by 1
Zhang, X., Guo, J., Zhang, D., Wang, Y., Shi, C., & Gong, Z. (2026) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2026.168215
Ramos, A., Aguilera‐Cortés, P., Farias, S., Pérez, I., Barros, V., Riveros, B., Soto, T., Ibáñez-Hernández, M. Á., Berríos-Pastén, C., Rojas, D., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.20.713133
Caractérisation de nouveaux inhibiteurs de la kinase RIPK1 et de la nécroptose
Cann, F. L. (2017) · theses.fr (ABES) · doi:10.70675/14750b73za612z432ezbf7cz5b72ea09e2e5
Régulation de la réponse immunitaire de la peau par le système nerveux sensoriel
Debroas, G. (2018) · theses.fr (ABES) · doi:10.70675/bbd33cc0z0f39z452bz9280zf155dc684d0f
Dynamique de la protéine Nox2 lors de la phagocytose
Joly, J. (2019) · theses.fr (ABES) · doi:10.70675/fc51395bzf826z4a8azaa87zfed7639d6143
Mazzoleni, V. (2020) · theses.fr (ABES) · doi:10.70675/e88b84afzf8b6z49cczb855z7c96c25470a2 · Cited by 2
Lysosomal autophagy in the treatment of inflammatory bowel disease
Retnakumar, S. V. (2022) · theses.fr (ABES) · doi:10.70675/addbfec8zdb85z4eddz9c05zb59b895dc6c0
Metadata
- Authors
- Remijsen, Q., Berghe, T. V., Wirawan, E., Asselbergh, B., Parthoens, E., De Rycke, R., Noppen, S., Delforge, M., Willems, J., & Vandenabeele, P.
- Affiliations
- KU Leuven (BE)
- Ghent University (BE)
- Universitair Ziekenhuis Leuven (BE)
- Corresponding author
- Willems, Jean
- Vandenabeele, Peter
- Venue
- Cell Research
- Published
- 2010-11-09
- Volume
- 21
- Issue
- 2
- Pages
- 290-304
- ISSN
- 1001-0602 (ISSN-L)
- 1748-7838
- PMC
- PMC3193439
- OpenAlex
- W2091512988
- Cited by
- 818
- References
- 51
- Citations by year
- 2026: 32 · 2025: 58 · 2024: 50 · 2023: 54 · 2022: 48 · 2021: 68 · 2020: 57 · 2019: 87 · 2018: 56 · 2017: 73 · 2016: 62 · 2015: 49 · 2014: 40 · 2013: 39 · 2012: 31
- FWCI
- 11.55
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- public-domain
- www.springer.com/tdm (tdm)
- Locations
- Cell Research (publishedVersion, public-domain)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Ghent University Academic Bibliography (Ghent University) (submittedVersion)
- Funders
- European Commission (200767)
- Universiteit Gent (01M00709)
- Vlaams Instituut voor Biotechnologie (BOF09/01M00709)
- Vlaamse regering (BOF09/01M00709)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Immunology and Microbiology › Microbiology › Antimicrobial Peptides and Activities
- Keywords
- neutrophil extracellular traps, NETosis, autophagy, superoxide, NADPH oxidase, chromatin decondensation, neutrophil cell death, apoptosis, chronic granulomatous disease, phorbol myristate acetate, innate immunity
- MeSH terms
- NADPH Oxidase 2, Autophagy, Granulomatous Disease, Chronic, Humans, Membrane Glycoproteins, NADH, NADPH Oxidoreductases, Neutrophils, Superoxides, Tetradecanoylphorbol Acetate, Apoptosis, NADPH Oxidases, Chromatin Assembly and Disassembly
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