The DOI matches its Crossref record; 61 of the 61 references it cites were found in a registry or an index.
Mitochondrial permeability transition pore is involved in oxidative burst and NETosis of human neutrophils
Open accessAbstract
Neutrophils release neutrophil extracellular traps (NETs) in response to numerous pathogenic microbes as the last suicidal resource (NETosis) in the fight against infection. Apart from the host defense function, NETs play an essential role in the pathogenesis of various autoimmune and inflammatory diseases. Therefore, understanding the molecular mechanisms of NETosis is important for regulating aberrant NET release. The initiation of NETosis after the recognition of pathogens by specific receptors is mediated by an increase in intracellular Ca 2+ concentration, therefore, the use of Ca 2+ ionophore A23187 can be considered a semi-physiological model of NETosis. Induction of NETosis by various stimuli depends on reactive oxygen species (ROS) produced by NADPH oxidase, however, NETosis induced by Ca 2+ ionophores was suggested to be mediated by ROS produced in mitochondria (mtROS). Using the mitochondria-targeted antioxidant SkQ1 and specific inhibitors of NADPH oxidase, we showed that both sources of ROS, mitochondria and NADPH oxidase, are involved in NETosis induced by A23187 in human neutrophils. In support of the critical role of mtROS, SkQ1-sensitive NETosis was demonstrated to be induced by A23187 in neutrophils from patients with chronic granulomatous disease (CGD). We assume that Ca 2+-triggered mtROS production contributes to NETosis either directly (CGD neutrophils) or by stimulating NADPH oxidase. The opening of the mitochondrial permeability transition pore (mPTP) in neutrophils treated by A23187 was revealed using the electron transmission microscopy as a swelling of the mitochondrial matrix. Using specific inhibitors, we demonstrated that the mPTP is involved in mtROS production, NETosis, and the oxidative burst induced by A23187.
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
“Mitochondrial ROS are involved in NOx activation and in the induction of classical NETosis by various stimuli [63,64].”
From The Role of Reactive Species on Innate Immunity (2022) · cites this paper as [64]
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
Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release
Zorov, D. B., Juhaszova, M., & Sollott, S. J. (2014) · Physiological Reviews · doi:10.1152/physrev.00026.2013 · Cited by 5,383
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
García-Romo, G. S., Caielli, S., Vega, B., Connolly, J., Allantaz, F., Xu, Z., Punaro, M., Baisch, J. M., Guiducci, C., Coffman, R. L., et al. (2011) · Science Translational Medicine · doi:10.1126/scitranslmed.3001201 · Cited by 1,429
Calcineurin: Form and Function
Rusnak, F. M., & Mertz, P. S. (2000) · Physiological Reviews · doi:10.1152/physrev.2000.80.4.1483 · Cited by 1,375
Neutrophil extracellular traps license macrophages for cytokine production in atherosclerosis
Warnatsch, A., Ιωάννου, Μ., Wang, Q., & Papayannopoulos, V. (2015) · Science · doi:10.1126/science.aaa8064 · Cited by 1,309
A Distinct Pathway Remodels Mitochondrial Cristae and Mobilizes Cytochrome c during Apoptosis
Scorrano, L., Ashiya, M., Buttle, K., Weiler, S., Oakes, S. A., Mannella, C. A., & Korsmeyer, S. J. (2002) · Developmental Cell · doi:10.1016/s1534-5807(01)00116-2 · Cited by 1,072
What is the mitochondrial permeability transition pore?
Halestrap, A. P. (2009) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2009.02.021 · Cited by 966
The Ca2+-induced membrane transition in mitochondria
Hunter, D. R., & Haworth, R. A. (1979) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(79)90371-0 · Cited by 872
Mitochondrial non-specific pores remain closed during cardiac ischaemia, but open upon reperfusion
Griffiths, E. J., & Halestrap, A. P. (1995) · Biochemical Journal · doi:10.1042/bj3070093 · Cited by 838
Cited by
Sorted by citations
NETosis: Molecular Mechanisms, Role in Physiology and Pathology
Vorobjeva, N. V., & Chernyak, B. V. (2020) · Biochemistry (Moscow) · doi:10.1134/s0006297920100065 · Cited by 559
Self-citationDiversity and complexity of cell death: a historical review
Park, W., Wei, S., Kim, B., Kim, B., Bae, S., Chae, Y. C., Ryu, D., & Ha, K. (2023) · Experimental & Molecular Medicine · doi:10.1038/s12276-023-01078-x · Cited by 381
The mitochondrial permeability transition pore: an evolving concept critical for cell life and death
Morciano, G., Naumova, N., Koprowski, P., Valente, S. A., Sardão, V. A., Potes, Y., Rimessi, A., Wieckowski, M. R., & Oliveira, P. J. (2021) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12764 · Cited by 161
Lu, T., Zhang, J., Cai, J., Xiao, J., Sui, X. Y., Yuan, X., Li, R., Li, Y., Yao, J., Lv, G., et al. (2022) · Biomaterials · doi:10.1016/j.biomaterials.2022.121486 · Cited by 150
The Role of Reactive Species on Innate Immunity
Andrés, C., Pérez de la Lastra, J., Juan, C., Plou, F., & Pérez-Lebeña, E. (2022) · Vaccines · doi:10.3390/vaccines10101735 · Cited by 142
Silwal, P., Kim, J. K., Kim, Y. J., & Jo, E. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01649 · Cited by 129
Mitochondria Related Cell Death Modalities and Disease
Tian, C., Liu, Y., Li, Z., Zhu, P., & Zhao, M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.832356 · Cited by 113
Mitochondria as Key Players in the Pathogenesis and Treatment of Rheumatoid Arthritis
Clayton, S. A., MacDonald, L., Kurowska‐Stolarska, M., & Clark, A. R. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.673916 · Cited by 100
Mitochondrial Reactive Oxygen Species in Infection and Immunity
Mukherjee, A., Ghosh, K. K., Chakrabortty, S., Gulyás, B. Z., Padmanabhan, P., & Ball, W. B. (2024) · Biomolecules · doi:10.3390/biom14060670 · Cited by 99
Mitochondrial control of innate immune responses
Chen, S., Liao, Z., & Xu, P. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1166214 · Cited by 87
Role of Extracellular Trap Release During Bacterial and Viral Infection
Schultz, B. M., Acevedo, O. A., Kalergis, A. M., & Bueno, S. M. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.798853 · Cited by 77
Yang, S., Li, X., Li, X., Wang, Z., Zhao, C., Li, Q., & Zhang, L. (2024) · International Journal of Biological Sciences · doi:10.7150/ijbs.97150 · Cited by 70
Mechanistic connections between mitochondrial biology and regulated cell death
Chipuk, J. E., Mohammed, J. N., Gelles, J. D., & Chen, Y. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.03.033 · Cited by 69
Redox signaling in innate immunity and inflammation: focus on macrophages and neutrophils
Braunstein, I., Motohashi, H., Dallenga, T. K., Schaible, U. E., & Benhar, M. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.06.006 · Cited by 75
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
NETosis as an oncologic therapeutic target: a mini review
Jaboury, S., Wang, K., O’Sullivan, K. M., Ooi, J. D., & Ho, G. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1170603 · Cited by 62
Yan, Z., He, Z., Jiang, H., Zhang, Y., Xu, Y., & Zhang, Y. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110651 · Cited by 59
Neutrophil Extracellular Traps: New Aspects
Vorobjeva, N. V. (2020) · Moscow University Biological Sciences Bulletin · doi:10.3103/s0096392520040112 · Cited by 57
Self-citationChen, J., Zhang, M., Zou, H., Aniagu, S. O., Jiang, Y., & Chen, T. (2023) · Toxicology · doi:10.1016/j.tox.2023.153466 · Cited by 50
Poles, M. Z., Nászai, A., Gulácsi, L., Czakó, B. L., Gál, K. G., Glenz, R. J., Dookhun, D., Rutai, A., Tallósy, S. P., Szabó, A., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.717157 · Cited by 49
Diverse Roles of NETosis in the Pathogenesis of Lupus
Wang, M., Ishikawa, T., Lai, Y., Nallapothula, D., & Singh, R. R. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.895216 · Cited by 51
Herring, S. E., Mao, S., Bhalla, M., Tchalla, E. Y. I., Kramer, J. M., & Ghanem, E. N. B. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1010700 · Cited by 45
Protein Kinase C Isoforms Mediate the Formation of Neutrophil Extracellular Traps
Vorobjeva, N. V., Dagil, Y. A., Pashenkov, M. V., Pinegin, B. V., & Chernyak, B. V. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.109448 · Cited by 43
Self-citationThe 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
Metabolic regulation of neutrophil functions in homeostasis and diseases
Leblanc, P.-O., Bourgoin, S. G., Poubelle, P. E., Tessier, P. A., & Pelletier, M. (2024) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiae025 · Cited by 44
Zhang, M., He, Q., Chen, G., & Li, P. A. (2020) · Neurodegenerative Diseases · doi:10.1159/000511207 · Cited by 42
Significance of Mast Cell Formed Extracellular Traps in Microbial Defense
Komi, D. E. A., & Kuebler, W. M. (2021) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-021-08861-6 · Cited by 45
Role of mitochondria in inflammatory lung diseases
Narala, V. R., Narala, S. R., Subramani, P. A., Panati, K., & Kolliputi, N. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1433961 · Cited by 43
Role of NETosis in Central Nervous System Injury
Chen, Y., Zhang, H., Hu, X., Cai, W., Ni, W., & Zhou, K. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/3235524 · Cited by 39
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
Zhu, Y., Wang, D., Luo, J., Jie, J., Liu, H., Peng, L., Bai, X., & Li, D. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/3990607 · Cited by 35
Established and emerging roles for mitochondria in neutrophils
Peng, S., Gao, J., Stojkov, D., Yousefi, S., & Simon, H. (2022) · Immunological Reviews · doi:10.1111/imr.13158 · Cited by 34
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
Neutrophils extracellular traps and ferroptosis in diabetic wounds
Huang, Y., Ding, Y., Wang, B., Ji, Q., Peng, C., & Tan, Q. (2023) · International Wound Journal · doi:10.1111/iwj.14231 · Cited by 34
Neutrophil extracellular traps in tumor metabolism and microenvironment
Liu, Z., Dou, Y., Lu, C., Han, R., & He, Y. (2025) · Biomarker Research · doi:10.1186/s40364-025-00731-z · Cited by 35
Neutrophils and NETs in Pathophysiology and Treatment of Inflammatory Bowel Disease
Ortega-Zapero, M., Gómez-Bris, R., Pascual-Laguna, I., Saéz, Á., & González, J. M. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26157098 · Cited by 41
A promising frontier: targeting NETs for stroke treatment breakthroughs
Fang, H., Bo, Y., Hao, Z., Mang, G., Jin, J., & Wang, H. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01563-4 · Cited by 32
Ferroptosis: A new strategy for traditional Chinese medicine treatment of stroke
Lou, Y., Ma, M., Jiang, Y., Xu, H., Gao, Z., Gao, L., & Wang, Y. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113806 · Cited by 32
Skulachev, V. P., Vyssokikh, M. Y., Chernyak, B. V., Mulkidjanian, A. Y., Skulachev, M. V., Shilovsky, G. A., Lyamzaev, K. G., Borisov, V. B., Severin, F. F., & Садовничий, В. А. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612540 · Cited by 35
Self-citationStages of NETosis Development upon Stimulation of Neutrophils with Activators of Different Types
Inozemtsev, V. A., Sergunova, V. A., Vorobjeva, N. V., Kozlova, E. K., Sherstyukova, E. A., Kandrashina, S., & Черныш, А. М. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241512355 · Cited by 30
Self-citationFedorov, A. V., Chelombitko, M. A., Chernyavskij, D. A., Galkin, I. I., Pletjushkina, O. Y., Vasilieva, T. V., Zinovkin, R. A., & Chernyak, B. V. (2022) · Cells · doi:10.3390/cells11213441 · Cited by 33
Self-citationXu, C., Ye, Z., Jiang, W., Wang, S., & Zhang, H. (2023) · Molecular Medicine · doi:10.1186/s10020-023-00758-8 · Cited by 30
Role of Mitochondria in the Regulation of Effector Functions of Granulocytes
Vorobjeva, N. V., Chelombitko, M. A., Sud’ina, G. F., Zinovkin, R. A., & Chernyak, B. V. (2023) · Cells · doi:10.3390/cells12182210 · Cited by 28
Self-citationPhenotypes and functions of “aged” neutrophils in cardiovascular diseases
Ling, S., & Xu, J. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.117324 · Cited by 29
A Web of Challenges: The Therapeutic Struggle to Target NETs in Disease
Espiritu, A., & O’Sullivan, K. M. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26104773 · Cited by 30
Sennett, C., & Pula, G. (2025) · Cells · doi:10.3390/cells14050335 · Cited by 28
Neutrophil extracellular traps: new aspects
Воробьева, Н. В. (2020) · Bulletin of Moscow University, Series 16. Biology (Moscow University) · Cited by 25
Cold air plasma improving rheumatoid arthritis via mitochondrial apoptosis pathway
Ding, C., Ni, L., Liu, Q., Zhou, C., Wang, G., Chu, P. K.-H., & Wu, Z. (2022) · Bioengineering & Translational Medicine · doi:10.1002/btm2.10366 · Cited by 21
Lou, X., Chen, H., Chen, S., Ji, H., He, T., Chen, H., Zhu, R., Le, Y., Sang, A., & Yu, Y. (2024) · The FASEB Journal · doi:10.1096/fj.202400656r · Cited by 21
Mitoptosis, Twenty Years After
Lyamzaev, K. G., Кнорре, Д. А., & Chernyak, B. V. (2020) · Biochemistry (Moscow) · doi:10.1134/s0006297920120020 · Cited by 21
Self-citationNeutrophils initiate proinflammatory immune responses in early endometriosis lesion development
Wilson, T. R., Peterson, K. R., Morris, S. A., Kuhnell, D., Kasper, S., & Burns, K. A. (2025) · JCI Insight · doi:10.1172/jci.insight.186133 · Cited by 22
Jie, S., Sun, H., Liu, J., Gao, Y., Bai, D., Zhu, L., Zhao, H., Zeng, H., & Ma, Y. (2022) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2022.116119 · Cited by 19
An emerging role for neutrophils in the pathogenesis of endometriosis
Wilson, T. R., Kasper, S., & Burns, K. A. (2025) · npj Women s Health · doi:10.1038/s44294-025-00059-x · Cited by 21
Sepsis‐induced NET formation requires MYD88 but is independent of GSDMD and PAD4
Englert, H., Rangaswamy, C., Kullik, G. A., Divivier, M., Göbel, J., Hermans‐Borgmeyer, I., Borgmeyer, U., Mowen, K. A., Beerens, M., Frye, M., et al. (2025) · The FASEB Journal · doi:10.1096/fj.202402514r · Cited by 18
NETosis in myocardial ischemia‑reperfusion injury: From mechanisms to therapies (Review)
Zhang, Z., Wang, Y., Li, T., & Wang, H. (2025) · Biomedical Reports · doi:10.3892/br.2025.1991 · Cited by 18
Zhang, T., Luu, M. D. A., Dolga, A. M., Eisel, U. L. M., & Schmidt, M. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1207280 · Cited by 16
Han, Y., Zhang, Q., Chen, L., Yang, D., & Zhao, J. (2021) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2021.104094 · Cited by 16
Immune landscape and redox imbalance during neurological disorders in COVID-19
Thakur, A., Sharma, V., Averbek, S., Liang, L., Pandya, N., Kumar, G., Cili, A., & Zhang, K. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06102-6 · Cited by 15
The role of selenoproteins in neutrophils during inflammation
Lee, T.-J., Nettleford, S. K., McGlynn, A., Carlson, B. A., Kirimanjeswara, G. S., & Prabhu, K. S. (2022) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2022.109452 · Cited by 15
Cell life-or-death events in osteoporosis: All roads lead to mitochondrial dynamics
Li, Z., Liang, S., Ke, L., Wang, M., Gao, K., Li, D., Xu, Z., Li, N., Zhang, P., & Cheng, W. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107383 · Cited by 14
Wang, Y., Shi, C., Guo, J., Zhang, Y., & Gong, Z. (2023) · Journal of Clinical and Translational Hepatology · doi:10.14218/jcth.2023.00132 · Cited by 13
Mitochondria-targeted antioxidant SkQ1 inhibits leukotriene synthesis in human neutrophils
Sud’ina, G. F., Golenkina, E. A., Prikhodko, A. S., Kondratenko, N. D., Gaponova, T. V., & Chernyak, B. V. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1023517 · Cited by 12
Self-citationXiao, Z., Wei, X., Li, M., Yang, K., Chen, R., Su, Y., Yu, Z., Liang, Y., & Ge, J. (2023) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2023.08.006 · Cited by 12
Advances in neutrophil extracellular traps and ferroptosis in sepsis-induced cardiomyopathy
Zeng, M., Niu, Y., Huang, J., & Deng, L. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1590313 · Cited by 15
Amirlatifi, S., Forouzin, S., Sadati, E., Moradpanah, S., Fazeli, R., Panahinia, P., Zarifi, N., & Rahimi, S. (2025) · Medical Oncology · doi:10.1007/s12032-025-02860-9 · Cited by 14
Wu, W., Meng, F., Zhang, H., Tian, H., & Zhang, X. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113051 · Cited by 11
Sepsis and heatstroke: overlapping and distinct mechanisms of systemic inflammation
Iba, T., Helms, J., Nagaoka, I., Kondo, Y., Ferrer, R., & Levy, J. H. (2025) · Inflammation Research · doi:10.1007/s00011-025-02145-x · Cited by 13
Rethinking neutrophil extracellular traps
Liu, Y., Ma, Y.-H., Yang, J.-W., Man, J.-W., Wang, H.-B., Li, Y., Liang, C., Cao, J., Chen, S., Li, K.-P., et al. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110834 · Cited by 12
Maqsood, M., Suntharalingham, S., Khan, M., Ortiz-Sandoval, C. G., Feitz, W. J. C., Palaniyar, N., & Licht, C. P. B. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25179625 · Cited by 13
Zhao, L., Li, T., Dang, M., Li, Y., Lu, J., Lu, Z., Chen, Z., Huang, Q., Chen, Y., Yang, Y., et al. (2025) · Advanced Science · doi:10.1002/advs.202411873 · Cited by 11
Mitochondria as Targets for Endothelial Protection in COVID-19
Chernyak, B. V., Popova, E. N., Zinovkina, L. A., Lyamzaev, K. G., & Zinovkin, R. A. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.606170 · Cited by 10
Self-citationHuang, G., Wu, H. M., Lin, B., Deng, D., Liu, Y., Qu, J., Xu, J., & Wang, B. (2025) · Seminars in Thrombosis and Hemostasis · doi:10.1055/a-2609-3457 · Cited by 11
iPCD: A Comprehensive Data Resource of Regulatory Proteins in Programmed Cell Death
Tang, D., Han, C., Lin, S., Tan, X., Zhang, W., Peng, D., Wang, C., & Xue, Y. (2022) · Cells · doi:10.3390/cells11132018 · Cited by 9
NADPH Oxidase Modulates Ca2+-Dependent Formation of Neutrophil Extracellular Traps
Vorobjeva, N. V., & Chernyak, B. V. (2020) · Moscow University Biological Sciences Bulletin · doi:10.3103/s0096392520030104 · Cited by 9
Self-citationChernyak, B. V., Lyamzaev, K. G., & Mulkidjanian, A. Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413480 · Cited by 10
Self-citationLive fast, die young: neutrophils streamline their metabolism to maximize inflammation
Holder, B. E., Reber, C. P., & Monteith, A. J. (2025) · Infection and Immunity · doi:10.1128/iai.00498-24 · Cited by 9
Mitochondria as Inducers of Neutrophil Extracellular Traps
Bečka, E., Hudecová, L., & Pastorek, M. (2026) · Inflammation · doi:10.1007/s10753-025-02432-z · Cited by 8
Golenkina, E. A., Viryasova, G. M., Galkina, S. I., Kondratenko, N. D., Gaponova, T. V., Romanova, Y. M., Lyamzaev, K. G., Chernyak, B. V., & Sud’ina, G. F. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1295150 · Cited by 8
Self-citationNeutrophil Extracellular Traps: Emerging Biomarker and Prototype of Functional Materials
Pang, B., Wen, L., Zheng, L., Jia, W. P., Xu, T., Song, Y., Li, J., & Wang, S. (2025) · Advanced Functional Materials · doi:10.1002/adfm.202425035 · Cited by 7
Jia, W., Zhang, J., Shang, Y., & Liu, S. (2025) · Cancer Letters · doi:10.1016/j.canlet.2025.218103 · Cited by 7
Sex differences in serum proteomic profiles in psoriatic arthritis
Dang, S., Li, X., Diao, L., Piguet, V., Croitoru, D. O., Wither, J., Jurišica, I., Chandran, V., & Eder, L. (2025) · Rheumatology · doi:10.1093/rheumatology/keaf311 · 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
Vorobjeva, N. V., Sud’ina, G. F., & Chernyak, B. V. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.609508 · Cited by 6
Self-citationChmielecki, A., Bortnik, K., Gałczyński, S., Padula, G., Jerczyńska, H., Stawski, R. S., & Nowak, D. (2022) · Biology · doi:10.3390/biology11010103 · Cited by 6
Lorestani, K., Ghorbanzade, S., Rahimi, S., Fazeli, R., Khdakarim, N., Hasanvand, A., & Hazari, V. (2025) · Molecular Biotechnology · doi:10.1007/s12033-025-01473-x · Cited by 5
Chen, S., Lin, J., Huang, J., Deng, L., & Zhang, Y. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1790788 · Cited by 4
Glukhareva, A. E., Afonin, G. V., Aa, M., Grivtsova, L. Y., Владимирович, К. И., Иванов, С. А., & Каприн, А. Д. (2023) · Journal of Modern Oncology · doi:10.26442/18151434.2022.4.201786 · Cited by 4
Tamoxifen triggers the in vitro release of neutrophil extracellular traps in healthy horses
Salinas, C., Barriga, K., Albornoz, A., Alarcón, P., Quiroga, J., Uberti, B., Sarmiento, J., Henríquez, C., Ehrenfeld, P., Burgos, R. A., et al. (2023) · Frontiers in Veterinary Science · doi:10.3389/fvets.2022.1025249 · Cited by 4
Lin, Y.-W., Jin, J., Han, Q., Hang, D., Chen, Z., Ye, S., Guo, Q., Huang, X.-Y., Li, J.-N., Zhang, H., et al. (2025) · Chemical Engineering Journal · doi:10.1016/j.cej.2025.166618 · Cited by 3
Adenovirus phagocytosis by neutrophils triggers a pro-inflammatory response
Laurans, S., Huerre, S., Dellis, O., Férard, C., Jalaber, H., Vanbergue, C., Brun, É., Jelin, R., Nüße, O., Benihoud, K., et al. (2026) · PLoS Pathogens · doi:10.1371/journal.ppat.1013504 · Cited by 3
Mitochondrial dysfunction in MASH: Focusing on chronic inflammation and intercellular communication
Luo, W., Yu, M., Zheng, C., Li, X., Ma, X., Zeng, G., Zhang, J., Ji, X., & Sun, L. (2026) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2026.153356 · Cited by 3
Mitochondrial metabolism in neutrophils: emerging roles in inflammatory skin diseases
Zhao, F., Gao, L., Guo, Y., Jiao, Y., Zou, W., Li, W., Li, W., Qi, R., & Wan, W. (2026) · British Journal of Dermatology · doi:10.1093/bjd/ljag060 · Cited by 3
Quiroga, J., Cortes, B., Sarmiento, J., Morán, G., & Henríquez, C. (2024) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2024.105151 · Cited by 3
Sveshnikova, A. N., Adamanskaya, E.-I. A., Korobkin, J.-J. D., & Panteleev, M. A. (2024) · Pediatric Hematology/Oncology and Immunopathology · doi:10.24287/1726-1708-2024-23-2-222-230 · Cited by 3
The Role of Protein Kinase C Isoforms in the Formation of Neutrophil Extracellular Traps
Vorobjeva, N. V., Vakhlyarskaya, S. S., & Chernyak, B. V. (2022) · Moscow University Biological Sciences Bulletin · doi:10.3103/s0096392522020122 · Cited by 3
Self-citationVorobjeva, N. V. (2023) · Moscow University Biological Sciences Bulletin · doi:10.3103/s0096392523010078 · Cited by 3
Self-citationMitochondrial Permeability Transition in Stem Cells, Development, and Disease
Dumbali, S. P., & Wenzel, P. L. (2022) · Advances in experimental medicine and biology · doi:10.1007/5584_2022_720 · Cited by 3
Senolytic therapy increases replicative capacity by eliminating senescent endothelial cells
Abdeahad, H., Moreno, D. G., Bloom, S. I., Huang, H., Lesniewski, L. A., & Donato, A. J. (2025) · Experimental Gerontology · doi:10.1016/j.exger.2025.112885 · Cited by 2
Zakrzewski, P., Rice, C. M., Naveh, C. A., Dowell, I., Fleming, K., Ramesh, A. V., Jones, R. L., Moura, P. L., Cela, D., Groves, S., et al. (2026) · EMBO Molecular Medicine · doi:10.1038/s44321-026-00453-1 · Cited by 3
NETs in ovarian cancer progression: innovative nanoparticle-based therapeutic strategies
Moradpanah, S., Aghaei, Z. H., Eslamnik, P., Goldiani, N. K., Sargolzaei, Z., Doosty, F., Barsam, M., Feli, M., & Zarifi, N. (2025) · European journal of medical research · doi:10.1186/s40001-025-03475-6 · Cited by 3
Metadata
- Authors
- Vorobjeva, N., Galkin, I., Pletjushkina, O., Golyshev, S., Zinovkin, R., Prikhodko, A., Pinegin, V., Kondratenko, I., Pinegin, B., & Chernyak, B.
- Affiliations
- Lomonosov Moscow State University (RU)
- Sechenov University (RU)
- Federal Medical-Biological Agency (RU)
- Corresponding author
- Vorobjeva, Nina
- ORCID
- Venue
- Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Publisher
- Elsevier BV
- Published
- 2020-05
- Volume
- 1866
- Issue
- 5
- Pages
- 165664
- ISSN
- 0925-4439 (ISSN-L)
- OpenAlex
- W2999533595
- Cited by
- 136
- References
- 61
- Citations by year
- 2026: 16 · 2025: 29 · 2024: 25 · 2023: 23 · 2022: 24 · 2021: 10 · 2020: 9
- FWCI
- 5.78
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Russian Foundation for Basic Research
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Keywords
- mitochondrial permeability transition pore, neutrophil extracellular traps, NETosis, respiratory burst, neutrophils, mitochondrial reactive oxygen species, NADPH oxidase, A23187, chronic granulomatous disease, SkQ1, mitochondrial swelling, intracellular calcium
- MeSH terms
- Calcimycin, Loss of Function Mutation, NADPH Oxidase 2, Mitochondrial Permeability Transition Pore, Adolescent, Calcium, Cations, Divalent, Cells, Cultured, Child, Electron Transport, Granulomatous Disease, Chronic, Humans, Male, Mitochondria, Neutrophils, Oxidation-Reduction, Plastoquinone, Free Radical Scavengers, Respiratory Burst, Reactive Oxygen Species, Mitochondrial Membrane Transport Proteins, Membrane Potential, Mitochondrial, Primary Cell Culture, Healthy Volunteers, Extracellular Traps
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