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 301–400 of 818
Innate and Adaptive Cell Populations Driving Inflammation in Dry Eye Disease
Reyes, J. L., Vannan, D. T., Eksteen, B., Juárez‐Avelar, I., Rodríguez, T., González, M. I., & Vázquez-Mendoza, A. (2018) · Mediators of Inflammation · doi:10.1155/2018/2532314 · Cited by 53
Zhou, Z., Zhang, S., Ding, S., Abudupataer, M., Zhang, Z., Zhu, X., Zhang, W., Zou, Y., Yang, X., Ge, J., et al. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/1209307 · Cited by 52
Alghamdi, M., Ghamdi, K. A. A., Khan, R. H., Uversky, V. N., & Redwan, E. M. M. M. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03237-8 · Cited by 52
Kao, T., Chen, P., Wang, Y., Tseng, H., Chang, S., Wu, T., Yang, S., Lee, Y., & Hwang, T. (2021) · British Journal of Pharmacology · doi:10.1111/bph.15597 · Cited by 51
Ullah, I., Ritchie, N. D., & Evans, T. J. (2017) · Innate Immunity · doi:10.1177/1753425917704299 · Cited by 50
Cao, Y., Shengchen, W., Sun, J., Shuting, W., & Zhang, Z. (2020) · Environmental Pollution · doi:10.1016/j.envpol.2020.114295 · 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
Vlachou, K., Mintzas, K., Glymenaki, M., Ιωάννου, Μ., Papadaki, G., Bertsias, G. K., Sidiropoulos, P. I., Boumpas, D. T., & Verginis, P. (2015) · Arthritis & Rheumatology · doi:10.1002/art.39441 · Cited by 51
Extracellular DNA traps released by acute promyelocytic leukemia cells through autophagy
Ma, R., Li, T., Cao, M., Si, Y., Wu, X., Zhao, L., Yao, Z., Zhang, Y., Fang, S., Deng, R., et al. (2016) · Cell Death and Disease · doi:10.1038/cddis.2016.186 · Cited by 50
Human Amniotic Membrane Mesenchymal Stem Cells inhibit Neutrophil Extracellular Traps through TSG-6
Magaña‐Guerrero, F. S., Domínguez-López, A., Martínez-Aboytes, P., Buentello‐Volante, B., & Garfias, Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-10962-2 · Cited by 50
Therapeutic Modulation of Autophagy in Leukaemia and Lymphoma
Djavaheri‐Mergny, M., Giuriato, S., Tschan, M. P., & Humbert, M. (2019) · Cells · doi:10.3390/cells8020103 · Cited by 52
Neutrophil Extracellular Traps: A Walk on the Wild Side of Exercise Immunology
Beiter, T., Fragasso, A., Hartl, D., & Niess, A. M. (2014) · Sports Medicine · doi:10.1007/s40279-014-0296-1 · Cited by 49
Heart failure with preserved ejection fraction: Defining the function of ROS and NO
Zuo, L., Chuang, C., Hemmelgarn, B. T., & Best, T. M. (2015) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01149.2014 · Cited by 49
Spontaneous formation of neutrophil extracellular traps is associated with autophagy
Guo, Y., Gao, F., Wang, X., Pan, Z., Wang, Q., Xu, S. S., Pan, S., Li, L., Zhao, D., & Qian, J. (2021) · Scientific Reports · doi:10.1038/s41598-021-03520-4 · Cited by 55
Misunderstandings Between Platelets and Neutrophils Build in Chronic Inflammation
Ramirez, G. A., Manfredi, A. A., & Maugeri, N. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02491 · Cited by 49
Arsenic trioxide promoting ETosis in acute promyelocytic leukemia through mTOR-regulated autophagy
Li, T., Ma, R., Zhang, Y., Mo, H., Yang, X., Hu, S., Wang, L., Novakovic, V. A., Chen, H., Kou, J., et al. (2018) · Cell Death and Disease · doi:10.1038/s41419-017-0018-3 · Cited by 45
The regulation of autophagy in the pesticide-induced toxicity: Angel or demon?
He, B., Wang, X., Yang, C., Zhu, J., Jin, Y., & Fu, Z. (2019) · Chemosphere · doi:10.1016/j.chemosphere.2019.125138 · Cited by 46
The role of autophagy in regulating metabolism in the tumor microenvironment
Zhang, P., Cheng, S., Sheng, X., Dai, H., He, K., & Du, Y. (2021) · Genes & Diseases · doi:10.1016/j.gendis.2021.10.010 · Cited by 46
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
Ivey, A. D., Fagan, B. M., Murthy, P., Lotze, M. T., Zeh, H. J., Hazlehurst, L., Geldenhuys, W. J., & Boone, B. A. (2023) · Clinical & Experimental Immunology · doi:10.1093/cei/uxad005 · Cited by 45
Xu, L., Zhang, W., Kwak, M., Zhang, L., Lee, P. C.-W., & Jin, J. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01371 · Cited by 48
Han, Z. H., Zhang, Y., Wang, C., Liu, X., Jiang, A., Liu, Z., Wang, J., Yang, Z., & Wei, Z. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.9b03155 · Cited by 45
Chiang, C.-C., Cheng, W.-J., Lin, C.-Y., Lai, K.-H., Ju, S.-C., Lee, C., Yang, S., & Hwang, T. (2019) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2019.112246 · Cited by 45
Autophagy-driven NETosis is a double-edged sword – Review
Liang, X., Liu, L., Wang, Y., Guo, H., Fan, H., Zhang, C., Hou, L., & Liu, Z. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110065 · Cited by 47
Li, X., Gao, Q., Wu, W., Hai, S., Hu, J., You, J., Huang, D., Wang, H., Wu, D., Han, M., et al. (2022) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2022.07.014 · Cited by 44
The emerging role of neutrophil extracellular traps in ulcerative colitis
Long, D., Mao, C., Xu, Y., & Zhu, Y. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1425251 · Cited by 50
Calo, G., Sabbione, F., Vota, D., Paparini, D., Ramhorst, R., Trevani, A. S., & Leirós, C. P. (2016) · Human Reproduction · doi:10.1093/humrep/dew292 · Cited by 44
van Dam, L. S., Rabelink, T. J., van Kooten, C., & Teng, Y. K. O. (2018) · Kidney International Reports · doi:10.1016/j.ekir.2018.11.005 · Cited by 46
Sultan, A. R., Hoppenbrouwers, T., Toom, N. A. L.-D., Snijders, S. V., van Neck, J. W., Verbon, A., de Maat, M. P. M., & van Wamel, W. J. B. (2019) · Infection and Immunity · doi:10.1128/iai.00605-19 · Cited by 46
Suzuki, É., Maverakis, E. M., Sarin, R., Bouchareychas, L., Kuchroo, V. K., Nestle, F. O., & Adamopoulos, I. E. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1600383 · Cited by 43
Tripathi, J. K., Sharma, A., Sukumaran, P., Sun, Y., Mishra, B. B., Singh, B. B., & Sharma, J. (2018) · The FASEB Journal · doi:10.1096/fj.201800605 · Cited by 43
Autophagy-mediated regulation of neutrophils and clinical applications
Yu, Y., & Sun, B. (2020) · Burns & Trauma · doi:10.1093/burnst/tkz001 · Cited by 45
Xu, J., Guo, B. K., Jia, B., Wang, M., Wen, P., Kan, T., Zhang, S., Liu, A., Tang, H., Yang, H., et al. (2024) · Bioactive Materials · doi:10.1016/j.bioactmat.2024.04.027 · Cited by 42
Effects of the antioxidants Trolox, Tiron and Tempol on neutrophil extracellular trap formation
Vorobjeva, N. V., & Pinegin, B. V. (2015) · Immunobiology · doi:10.1016/j.imbio.2015.09.005 · Cited by 42
Immunothrombosis in COVID-19: Implications of Neutrophil Extracellular Traps
Bautista-Becerril, B., Campi-Caballero, R., Sevilla-Fuentes, S., Hernández-Regino, L. M., Hanono, A., Flores-Bustamante, A., González-Flores, J., García-Ávila, C., Aquino‐Gálvez, A., Castillejos-López, M. D. J., et al. (2021) · Biomolecules · doi:10.3390/biom11050694 · Cited by 44
Zhu, C., Xie, J., Zhao, Z., Li, P., Liu, Q., Guo, Y., Meng, Y., Wan, X., Bian, J., Deng, X., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.949217 · Cited by 42
Li, J., Li, W., Han, Z., Zhong, C., & Zhang, Q. (2020) · EBioMedicine · doi:10.1016/j.ebiom.2019.102600 · Cited by 41
Morandini, L., Avery, D., Angeles, B., Winston, P., Martin, R. K., Donahue, H. J., & Olivares-Navarrete, R. (2023) · Acta Biomaterialia · doi:10.1016/j.actbio.2023.05.016 · Cited by 40
Gunderson, C. W., & Seifert, H. S. (2015) · mBio · doi:10.1128/mbio.02452-14 · Cited by 40
Giaglis, S., Hahn, S., & Hasler, P. (2016) · Frontiers in Pediatrics · doi:10.3389/fped.2016.00097 · Cited by 40
“NETtling” the host: Breaking of tolerance in chronic inflammation and chronic infection
Skopelja‐Gardner, S., Jones, J. D. G., & Rigby, W. F. C. (2017) · Journal of Autoimmunity · doi:10.1016/j.jaut.2017.10.008 · Cited by 39
Zhang, Q., Wang, S., Zheng, S., Zhang, Z., & Xu, S. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/1763589 · Cited by 39
RetractedThe Immunomodulatory Effect of Alpha-Lipoic Acid in Autoimmune Diseases
Liu, W., Shi, L., & Li, S. (2019) · BioMed Research International · doi:10.1155/2019/8086257 · Cited by 40
The power from within – understanding the driving forces of neutrophil extracellular trap formation
Neubert, E., Meyer, D., Kruss, S., & Erpenbeck, L. (2020) · Journal of Cell Science · doi:10.1242/jcs.241075 · Cited by 42
Role of Neutrophils in Systemic Vasculitides
Michailidou, D., Mustelin, T., & Lood, C. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.619705 · Cited by 39
Mateo‐Otero, Y., Zambrano, F., Catalán, J., Sánchez, R., Yeste, M., Miró, J., & Fernández-Fuertes, B. (2021) · Equine Veterinary Journal · doi:10.1111/evj.13457 · Cited by 41
Arcos, J., Diangelo, L., Scordo, J. M., Sasindran, S. J., Moliva, J. I., Turner, J., & Torrelles, J. B. (2015) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiv146 · Cited by 38
Gillenius, E., & Urban, C. F. (2015) · Microbes and Infection · doi:10.1016/j.micinf.2014.12.014 · Cited by 39
Moussavi-Harami, S. F., Mladinich, K. M., Sackmann, E. K., Shelef, M. A., Starnes, T. W., Guckenberger, D. J., Huttenlocher, A., & Beebe, D. J. (2016) · Integrative Biology · doi:10.1039/c5ib00225g · Cited by 40
Roles of Autophagy and Autophagy-Related Proteins in Antifungal Immunity
Kanayama, M., & Shinohara, M. L. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00047 · Cited by 40
The role of autophagy in the pathogenesis of systemic lupus erythematosus
Liu, X., Qin, H., & Xu, J. (2016) · International Immunopharmacology · doi:10.1016/j.intimp.2016.09.017 · Cited by 39
Agarwal, S., Loder, S. J., Cholok, D. J., Li, J., Bian, G., Yalavarthi, S., Li, S., Carson, W. F., Hwang, C. D., Marini, S., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02148 · Cited by 39
Challenges in the characterization of neutrophil extracellular traps: The truth is in the details
Naccache, P. H., & Fernandes, M. J. (2015) · European Journal of Immunology · doi:10.1002/eji.201546022 · Cited by 38
Liu, C., Qi, J., Shan, B., Gao, R., Gao, F., Xie, H., Yuan, M., Liu, H., Jin, S., Wu, F., et al. (2018) · International Immunopharmacology · doi:10.1016/j.intimp.2018.10.030 · Cited by 37
Liu, S., Yue, Y., Pan, P., Zhang, L., Su, X., Li, H., Li, H., Li, Y., Dai, M., Li, Q., et al. (2018) · Inflammation · doi:10.1007/s10753-018-0903-7 · Cited by 39
Low Production of Reactive Oxygen Species Drives Systemic Lupus Erythematosus
Urbonaviciute, V., Luo, H., Sjöwall, C., Bengtsson, A. A., & Holmdahl, R. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2019.06.001 · Cited by 37
Dong, Y., Jin, C., Ding, Z., Zhu, Y., He, Q., Zhang, X., Ai, R., Yin, Y., & He, Y. (2020) · Pediatric Research · doi:10.1038/s41390-020-0964-9 · Cited by 37
Targeting neutrophil extracellular traps in severe acute pancreatitis treatment
Hu, J., Kang, H., Chen, H., Yao, J., Yi, X.-L., Tang, W., & Wan, M. (2020) · Therapeutic Advances in Gastroenterology · doi:10.1177/1756284820974913 · Cited by 37
Li, S., Ma, Y., Ye, S., Hu, D., & Xiao, F. (2021) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2021.126758 · Cited by 37
Li, H., Itagaki, K., Sandler, N., Gallo, D. J., Galenkamp, A., Kaczmarek, E., Livingston, D. H., Zeng, Y., Lee, Y. T., Tang, I. T., et al. (2015) · The Journal of Trauma: Injury, Infection, and Critical Care · doi:10.1097/ta.0000000000000509 · Cited by 37
Neutrophil extracellular traps in dermatology: Caught in the NET
Hoffmann, J. H. O., & Enk, A. (2016) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2016.07.001 · Cited by 37
Neutrophil Extracellular Traps: Inflammation and Biomaterial Preconditioning for Tissue Engineering
Fetz, A. E., & Bowlin, G. L. (2022) · Tissue Engineering Part B: Reviews · doi:10.1089/ten.teb.2021.0013 · Cited by 36
Fine-tuning neutrophil activation: Strategies and consequences
van der Linden, M., & Meyaard, L. (2016) · Immunology Letters · doi:10.1016/j.imlet.2016.05.015 · Cited by 36
Neutrophil Extracellular Traps: Formation and Involvement in Disease Progression.
Kumar, S., Gupta, E., Kaushik, S., & Jyoti, A. (2018) · PubMed · Cited by 34
Cannabidiol Modifies the Formation of NETs in Neutrophils of Psoriatic Patients
Wójcik, P., Garley, M., Wroński, A., Jabłońska, E., & Skrzydlewska, E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186795 · Cited by 36
Jiang, H., Lu, Q., Xu, J., Huo, G., Cai, Y., Geng, S., Xu, H., Zhang, J., Li, H., Yuan, K., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-30922-3 · Cited by 36
The emerging role of neutrophil extracellular traps in autoimmune and autoinflammatory diseases
Zeng, L., Xiang, W., Xiao, W., Wu, Y., & Sun, L. (2025) · MedComm · doi:10.1002/mco2.70101 · Cited by 37
Ostafin, M., Pruchniak, M. P., Ciepiela, O., Reznick, A. Z., & Demkow, U. A. (2016) · Analytical Biochemistry · doi:10.1016/j.ab.2016.05.003 · Cited by 35
Anthracyclines Suppress Both NADPH Oxidase- Dependent and -Independent NETosis in Human Neutrophils
Khan, M. A., D’Ovidio, A., Tran, H., & Palaniyar, N. (2019) · Cancers · doi:10.3390/cancers11091328 · Cited by 35
Ticagrelor Exerts Immune-Modulatory Effect by Attenuating Neutrophil Extracellular Traps
Mitsios, A., Chrysanthopoulou, A., Αραμπατζιόγλου, Α., Angelidou, I., Vidali, V. P., Ritis, K., Skendros, P., & Stakos, D. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103625 · Cited by 35
Yang, X., Ma, Y., Chen, X., Zhu, J., Xue, W., & Ning, K. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121867 · Cited by 36
Xiang, D.-D., Sun, Y.-X., Chen, J., Guo, Y.-Q., Fei, Y.-X., Ren, B.-Q., He, X.-T., & Li, X. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04441-z · Cited by 34
Zearalenone Induces Estrogen-Receptor-Independent Neutrophil Extracellular Trap Release in Vitro
Wang, J., Wei, Z., Han, Z. H., Liu, Z., Zhu, X., Li, X., Wang, K., & Yang, Z. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.8b05948 · Cited by 34
Besnoitia besnoitibradyzoite stages induce suicidal- and rapid vital-NETosis
Zhou, E., Silva, L. M. R., Conejeros, I., Velásquez, Z. D., Hirz, M., Gärtner, U., Jacquiet, P., Taubert, A., & Hermosilla, C. R. (2019) · Parasitology · doi:10.1017/s0031182019001707 · Cited by 35
Characteristics and Role of Neutrophil Extracellular Traps in Asthma
Chen, F., Yu, M. H., Zhong, Y., Wang, L., & Huang, H. (2021) · Inflammation · doi:10.1007/s10753-021-01526-8 · Cited by 36
Role of neutrophil extracellular traps in inflammatory evolution in severe acute pancreatitis
Kang, H., Yang, Y., Zhu, L., Zhao, X., Li, J., Tang, W., & Wan, M. (2022) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002359 · Cited by 34
Autophagy mediates neutrophil responses to bacterial infection
Chargui, A., & May, M. V. E. (2014) · Apmis · doi:10.1111/apm.12271 · Cited by 35
In vitro study: HIF-1α-dependent glycolysis enhances NETosis in hypoxic conditions
Ye, Y., Wang, Y., Xu, Q., Liu, J., Yang, Z., Wuren, T., & Ge, R.-L. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1583587 · Cited by 35
Molecular analyses on Neospora caninum -triggered NETosis in the caprine system
Villagra-Blanco, R., Silva, L. M. R., Gärtner, U., Wagner, H., Failing, K., Wehrend, A., Taubert, A., & Hermosilla, C. R. (2017) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2017.02.020 · Cited by 33
Martín‐Sánchez, D., Fontecha‐Barriuso, M., Sánchez-Niño, M. D., Ramos, A. M., Benavente, R. C., Enguita, C. G., Linkermann, A., Sanz, A. B., & Ortíz, A. (2018) · Cell Death and Disease · doi:10.1038/s41419-017-0043-2 · Cited by 35
Kim, J.-K., Park, M. J., Lee, H. W., Lee, H., Choi, S. R., Song, Y. R., Kim, H. J., Park, H. C., & Kim, S. G. (2018) · Clinical Immunology · doi:10.1016/j.clim.2018.10.003 · Cited by 33
Furanoid F-Acid F6 Uniquely Induces NETosis Compared to C16 and C18 Fatty Acids in Human Neutrophils
Khan, M. A., Pace-Asciak, C. R., Al‐Hassan, J. M., Afzal, M., Liu, Y., Oommen, S., Paul, B. M., Nair, D., & Palaniyar, N. (2018) · Biomolecules · doi:10.3390/biom8040144 · Cited by 33
Zhou, E., Conejeros, I., Velásquez, Z. D., Muñoz-Caro, T., Gärtner, U., Hermosilla, C. R., & Taubert, A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01131 · Cited by 33
The IRE1α Stress Signaling Axis Is a Key Regulator of Neutrophil Antimicrobial Effector Function
Abuaita, B. H., Sule, G. J., Schultz, T. L., Gao, F., Knight, J. S., & O’Riordan, M. X. (2021) · The Journal of Immunology · doi:10.4049/jimmunol.2001321 · Cited by 33
Extracellular DNA Traps: Origin, Function and Implications for Anti-Cancer Therapies
Mamtimin, M., Pinarci, A., Han, C., Braun, A., Anders, H., Gudermann, T. W., & Mammadova‐Bach, E. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.869706 · Cited by 35
Myocardial injury: where inflammation and autophagy meet
Liu, C., Liu, Y., Chen, H., Yang, X., Lu, C., Wang, L., & Lu, J. (2023) · Burns & Trauma · doi:10.1093/burnst/tkac062 · Cited by 33
Svobodová, E., Staib, P., Losse, J., Hennicke, F., Barz, D., & Józsi, M. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1200185 · Cited by 35
Oxidation and mitochondrial origin of NET DNA in the pathogenesis of lupus
Muller, S., & Radic, M. Z. (2016) · Nature Medicine · doi:10.1038/nm.4044 · Cited by 33
Neutrophil extracellular traps in fungal infections: A seesaw battle in hosts
Zhong, H., Lu, R.-Y., & Wang, Y. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.977493 · Cited by 33
Itoh, H., Matsuo, H., Kitamura, N., Yamamoto, S., Higuchi, T., Takematsu, H., Kamikubo, Y., Kondo, T., Yamashita, K., Sasada, M., et al. (2015) · Journal of Leukocyte Biology · doi:10.1189/jlb.4a0813-422rrr · Cited by 33
Neutrophil Extracellular Traps Open the Pandora’s Box in Severe Malaria
Boeltz, S., Munoz, L. E., Fuchs, T. A., & i, M. H. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00874 · Cited by 32
Lv, X., Liu, S., Li, K., Cui, B., Liu, C., & Hu, Z. (2017) · Oncotarget · doi:10.18632/oncotarget.20353 · Cited by 32
Yin, K., Yang, Z., Gong, Y., Wang, D., & Lin, H. (2019) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2019.02.033 · Cited by 32
Neutrophil Extracellular Traps: Current Perspectives in the Eye
Estúa-Acosta, G. A., Zamora-Ortiz, R., Buentello‐Volante, B., García-Mejía, M., & Garfias, Y. (2019) · Cells · doi:10.3390/cells8090979 · Cited by 34
Yin, K., Cui, Y., Qu, Y., Zhang, J., Zhang, H., & Lin, H. (2020) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2020.110412 · Cited by 32
Mazzoleni, V., Zimmermann, K., Smirnova, A., Tarassov, I., & Prévost, G. (2020) · The FASEB Journal · doi:10.1096/fj.201902981r · Cited by 32
Role of Neutrophils on the Ocular Surface
Mun, Y., Hwang, J. S., & Shin, Y. J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910386 · Cited by 35
Hwang, T., Hsu, C., Aljuffali, I. A., Chen, C.-H., Chang, Y.-T., & Fang, J. (2015) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2015.02.022 · Cited by 32
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