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NETosis: Molecular Mechanisms, Role in Physiology and Pathology
Open accessAbstract
NETosis is a program for formation of neutrophil extracellular traps (NETs), which consist of modified chromatin decorated with bactericidal proteins from granules and cytoplasm. Various pathogens, antibodies and immune complexes, cytokines, microcrystals, and other physiological stimuli can cause NETosis. Induction of NETosis depends on reactive oxygen species (ROS), the main source of which is NADPH oxidase. Activation of NADPH oxidase depends on increase in the concentration of Ca2+ in the cytoplasm and in some cases on the generation of ROS in mitochondria. NETosis includes release of the granule components into the cytosol, modification of histones leading to chromatin decondensation, destruction of the nuclear envelope, as well as formation of pores in the plasma membrane. In this review, basic mechanisms of NETosis, as well as its role in the pathogenesis of some diseases including COVID-19 are discussed.
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“Vital NETosis helps contain local infections by allowing PMNs to rapidly release NETs and continue to phagocytose live bacteria.”
From The Role of Reactive Species on Innate Immunity (2022) · cites this paper as [66]
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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
COVID-19: consider cytokine storm syndromes and immunosuppression
Mehta, P., McAuley, D. F., Brown, M., Sanchez, E., Tattersall, R. S., & Manson, J. J. (2020) · The Lancet · doi:10.1016/s0140-6736(20)30628-0 · Cited by 9,664
Galluzzi, L., Vitale, I., Aaronson, S. A., Abrams, J. M., Adam, D., Agostinis, P., Alnemri, E. S., Altucci, L., Amelio, I., Andrews, D. W., et al. (2018) · Cell Death & Differentiation · doi:10.1038/s41418-017-0012-4 · Cited by 6,680
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
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
Neutrophil elastase and myeloperoxidase regulate the formation of neutrophil extracellular traps
Papayannopoulos, V., Metzler, K. D., Hakkim, A., & Zychlinsky, A. (2010) · Journal of Cell Biology · doi:10.1083/jcb.201006052 · Cited by 2,103
THE MITOCHONDRIAL DEATH/LIFE REGULATOR IN APOPTOSIS AND NECROSIS
Kroemer, G., Dallaporta, B., & Resche-Rigon, M. (1998) · Annual Review of Physiology · doi:10.1146/annurev.physiol.60.1.619 · Cited by 1,975
Neutrophil extracellular traps in COVID-19
Zuo, Y., Yalavarthi, S., Shi, H., Gockman, K., Zuo, M., Madison, J. A., Blair, C., Weber, A. G., Barnes, B. J., Egeblad, M., et al. (2020) · JCI Insight · doi:10.1172/jci.insight.138999 · Cited by 1,598
Lood, C., Blanco, L. P., Purmalek, M. M., Carmona-Rivera, C., De Ravin, S. S., Smith, C. K., Malech, H. L., Ledbetter, J. A., Elkon, K. B., & Kaplan, M. J. (2016) · Nature Medicine · doi:10.1038/nm.4027 · Cited by 1,570
Rogers, C., Fernandes-Alnemri, T., Mayes, L., Alnemri, D., Cingolani, G., & Alnemri, E. S. (2017) · Nature Communications · doi:10.1038/ncomms14128 · Cited by 1,510
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Favale, G., Donnarumma, F., Capone, V., Torre, L. D., Beato, A., Carannante, D., Verrilli, G., Nawaz, A., Grimaldi, F., Simone, M. C. D., et al. (2024) · Cancers · doi:10.3390/cancers16091657 · Cited by 6
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Wang, Y., Guo, J., Zhang, D., Shi, C., Zhang, X., & Gong, Z. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113270 · Cited by 6
Sharma, N., Bhat, S. H., Mathew, B., Yadav, M., Tripathi, G., Bindal, V., Yadav, S., Sharma, N., Pandey, S., Hemati, H., et al. (2024) · Molecular Therapy Oncology · doi:10.1016/j.omton.2024.200904 · Cited by 7
Wu, C., Ren, Y., Yang, L., Cui, Y., Zhang, L., Zhang, P., Zhang, X., Kan, S., Zhang, C., & Xiong, Y. (2025) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.4c02318 · Cited by 6
Şahin, F., Breinbauer, R., Linnemann, C., Tombaz, M., Nussler, A. K., & Ehnert, S. (2025) · Methods and Protocols · doi:10.3390/mps8020042 · Cited by 6
Sun, Y., Liu, H., Jiang, J., Hu, L., Ma, Q., Li, X., Liu, T., & Gu, X. (2025) · Nutrients · doi:10.3390/nu17132242 · Cited by 6
Al-Sharif, N., Qaisi, M., Shaul, M. E., Kaisar-Iluz, N., Padawer, D., Bouhanna, O., Volman, Y., & Fridlender, Z. G. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1643609 · Cited by 6
Velur, V., McCulloch, P. C., Taraballi, F., & Niclot, F. B. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262010117 · Cited by 6
Melamud, M. M., Tolmacheva, A. S., Сизиков, А. Э., Klyaus, N. A., Zhuravlev, E. S., Stepanov, G. A., Nevinsky, G. A., Buneva, V. N., & Ermakov, E. A. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262412127 · Cited by 7
Effector function and neutrophil cell death in the severity of sepsis with diabetes mellitus
Margalin, B., Arfijanto, M. V., & Hadi, U. (2024) · Narra J · doi:10.52225/narra.v4i1.532 · Cited by 6
Sveshnikova, A. N., Adamanskaya, E.-I. A., & Panteleev, M. A. (2024) · Pediatric Hematology/Oncology and Immunopathology · doi:10.24287/1726-1708-2024-23-1-211-218 · Cited by 6
Ji, Z., Zhang, C., Yuan, J., He, Q., Zhang, X., Yang, D., Xu, N., & Chu, J. (2024) · PLoS ONE · doi:10.1371/journal.pone.0298775 · Cited by 6
Investigation of Extracted Plasma Cell-Free DNA as a Biomarker in Foals with Sepsis
Hobbs, K. J., Cooper, B. L., Dembek, K. A., & Sheats, M. K. (2024) · Veterinary Sciences · doi:10.3390/vetsci11080346 · Cited by 6
Berillo, O., & Schiffrin, E. L. (2024) · Canadian Journal of Cardiology · doi:10.1016/j.cjca.2024.08.270 · Cited by 6
Tzang, B., Chin, H.-Y., Tzang, C.-C., Chuang, P.-H., Chen, D., & Hsu, T. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25189917 · Cited by 6
Paramasivam, S., Murugesan, J., Vedagiri, H., Perumal, S. S., & Ekambaram, S. P. (2024) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-024-01600-6 · Cited by 6
Structural studies of the IFNλ4 receptor complex using cryoEM enabled by protein engineering
Grubbe, W. S., Zhang, B., Kauffman, A., Byléhn, F., Padoł, K., Jung, H.-G., Park, S. B., Priest, J. M., Özkan, E., Pablo, J., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-56119-y · Cited by 6
Vaspin identified as a DNA ‐binding serpin with functional consequences for protease inhibition
Möhlis, K., Useini, A., Betat, H., Bonin, S., Broghammer, H., Nuwayhid, R., Langer, S., Mörl, M., Sträter, N., & Heiker, J. T. (2025) · FEBS Journal · doi:10.1111/febs.70270 · Cited by 6
Ciepiela, O., Małecka‐Giełdowska, M., & Czyżewska, E. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10225243 · Cited by 6
Michalska, M. N., Grochowiecki, T., Jakimowicz, T., & Nazarewski, S. (2021) · Medical Science Monitor · doi:10.12659/msm.935134 · Cited by 6
Lü, P., Zhu, X., Qin, Z., Liu, J., Song, E., & Song, Y. (2022) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.1c00375 · Cited by 6
Bonilla, M. C., Lassnig, S., Corella, A. O., Imker, R., Valentin‐Weigand, P., von Köckritz‐Blickwede, M., Luther, A., Hennig‐Pauka, I., & de Buhr, N. (2022) · Pathogens · doi:10.3390/pathogens11080880 · Cited by 6
Metadata
- Authors
- Vorobjeva, N. V., & Chernyak, B. V.
- Affiliations
- Lomonosov Moscow State University (RU)
- Corresponding author
- Vorobjeva, N. V.
- Venue
- Biochemistry (Moscow)
- Publisher
- Pleiades Publishing Ltd
- Published
- 2020-10
- Volume
- 85
- Issue
- 10
- Pages
- 1178-1190
- ISSN
- 0006-2979 (ISSN-L)
- 1608-3040
- PMC
- PMC7590568
- OpenAlex
- W3095535158
- Cited by
- 559
- References
- 111
- Citations by year
- 2026: 84 · 2025: 128 · 2024: 149 · 2023: 96 · 2022: 71 · 2021: 31
- FWCI
- 4.83
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Biochemistry (Moscow) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Russian Foundation for Basic Research
- Lomonosov Moscow State University
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Life Sciences › Immunology and Microbiology › Microbiology › Antimicrobial Peptides and Activities
- Health Sciences › Medicine › Hematology › Blood disorders and treatments
- Keywords
- NETosis, neutrophil extracellular traps, neutrophils, NADPH oxidase, reactive oxygen species, calcium signaling, mitochondrial reactive oxygen species, histone modifications, chromatin decondensation, granule exocytosis, immune complexes, cytokines, microcrystals, COVID-19 pathogenesis
- MeSH terms
- COVID-19, SARS-CoV-2, Calcium, Chromatin, Histones, Humans, Mitochondria, Neutrophils, Reactive Oxygen Species, Oxidative Stress, NADPH Oxidases, Extracellular Traps
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