The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.
The NLRP3 inflammasome is released as a particulate danger signal that amplifies the inflammatory response
Open accessAbstract
Assembly of the NLRP3 inflammasome activates caspase-1 and mediates the processing and release of the leaderless cytokine IL-1β and thereby serves a central role in the inflammatory response and in diverse human diseases. Here we found that upon activation of caspase-1, oligomeric NLRP3 inflammasome particles were released from macrophages. Recombinant oligomeric protein particles composed of the adaptor ASC or the p.D303N mutant form of NLRP3 associated with cryopyrin-associated periodic syndromes (CAPS) stimulated further activation of caspase-1 extracellularly, as well as intracellularly after phagocytosis by surrounding macrophages. We found oligomeric ASC particles in the serum of patients with active CAPS but not in that of patients with other inherited autoinflammatory diseases. Our findings support a model whereby the NLRP3 inflammasome, acting as an extracellular oligomeric complex, amplifies the inflammatory response.
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
“They can also be recognized by neighboring microglia as a danger signal and induce inflammatory responses including activation of the NLRP3 inflammasome, thereby propagating inflammation [70–72].”
From Microglial function, INPP5D/SHIP1 signaling, and NLRP3 inflammasome activation: implications for Alzheimer’s disease (2023) · cites this paper as [71]
In the citing paper
“In turn, NLRP3 inflammasome activity leads to the extracellular release of ASC particles that may function as danger signals (246).”
From The gut-brain axis: how microbiota and host inflammasome influence brain physiology and pathology (2020) · cites this paper as [246]
In the citing paper
“Increased expression and activity of the NLRP3 inflammasome machinery in circulating immune cells of patients affected by depression (245), bipolar disorder (246), and ASD (226), have been reported.”
From The gut-brain axis: how microbiota and host inflammasome influence brain physiology and pathology (2020) · cites this paper as [246]
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
Schroder, K., & Tschopp, J. (2010) · Cell · doi:10.1016/j.cell.2010.01.040 · Cited by 5,475
Gout-associated uric acid crystals activate the NALP3 inflammasome
Martinon, F., Pétrilli, V., Mayor, A., Tardivel, A., & Tschopp, J. (2006) · Nature · doi:10.1038/nature04516 · Cited by 5,326
NLRP3 inflammasomes are required for atherogenesis and activated by cholesterol crystals
Duewell, P., Kono, H., Rayner, K. J., Sirois, C. M., Vladimer, G., Bauernfeind, F. G., Abela, G. S., Franchi, L., Nuñez, G., Schnurr, M., et al. (2010) · Nature · doi:10.1038/nature08938 · Cited by 4,026
Immunological and inflammatory functions of the interleukin-1 family
Dinarello, C. A. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132612 · Cited by 3,466
Cryopyrin activates the inflammasome in response to toxins and ATP
Mariathasan, S., Weiss, D. S., Newton, K., McBride, J., O'Rourke, K., Roose-Girma, M., Lee, W. P., Weinrauch, Y., Monack, D. M., & Dixit, V. M. (2006) · Nature · doi:10.1038/nature04515 · Cited by 3,080
Hornung, V., Bauernfeind, F., Halle, A., Samstad, E. O., Kono, H., Rock, K. L., Fitzgerald, K. A., & Latz, E. (2008) · Nature Immunology · doi:10.1038/ni.1631 · Cited by 3,065
Nakahira, K., Haspel, J. A., Rathinam, V. A. K., Lee, S.-J., Dolinay, T., Lam, H. C., Englert, J. A., Rabinovitch, M., Cernadas, M., Kim, H. P., et al. (2011) · Nature Immunology · doi:10.1038/ni.1980 · Cited by 3,049
Thioredoxin-interacting protein links oxidative stress to inflammasome activation
Zhou, R., Tardivel, A., Thorens, B., Choi, I., & Tschopp, J. (2010) · Nature Immunology · doi:10.1038/ni.1831 · Cited by 2,708
The NALP3 inflammasome is involved in the innate immune response to amyloid-β
Halle, A., Hornung, V., Petzold, G. C., Stewart, C. R., Monks, B. G., Reinheckel, T., Fitzgerald, K. A., Latz, E., Moore, K. J., & Golenbock, D. T. (2008) · Nature Immunology · doi:10.1038/ni.1636 · Cited by 2,441
Cited by
Sorted by citations
Items 601–700 of 789
Евгеньевна, К. К., Wegner, E. A., & Барбараш, О. Л. (2022) · Kardiologiia · doi:10.18087/cardio.2022.3.n1206 · Cited by 7
Liu, W., Zhou, H., Dong, H., Xing, D., & Lu, M. (2023) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-023-01176-7 · Cited by 6
Cell organelles are retained inside pyroptotic corpses during inflammatory cell death
Hempel, A., D’Osualdo, A., Snipas, S. J., & Salvesen, G. S. (2023) · Bioscience Reports · doi:10.1042/bsr20231265 · Cited by 6
Vega, M. T. M., Matilla, J., Bazán, E., Reimers, D., de Andrés-Martín, A., Gonzalo‐Gobernado, R., Corrêa, C., Urbano, F., & Gómez‐Coronado, D. (2024) · Cells · doi:10.3390/cells13060536 · Cited by 6
Sun, X., Bin, K., Dai, Y., Xiong, C., Li, M., & Luo, Z. (2020) · Clinical Hemorheology and Microcirculation · doi:10.3233/ch-200842 · Cited by 6
Molecular Mechanisms and Functions of lncRNAs in the Inflammatory Reaction of Diabetes Mellitus
Huang, L., & Hu, X. (2021) · International Journal of Endocrinology · doi:10.1155/2021/2550399 · Cited by 6
Zhang, K., Liu, Y., Zhao, Y., Guo, Q., An, S., & Wu, S. (2023) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2023.101482 · Cited by 6
Signaling cascades and inflammasome activationin microbial infections
Ali, S. R., Karin, M., & Nizet, V. (2016) · Inflammasome · doi:10.1515/infl-2015-0002 · Cited by 9
“Recent reports on extracellular inflammasome formation supports the notion of importance of NLR activation to the neighboring cells [45, 46], however the role of signaling pathways in release and activation of extracellular NLRs remains unknown.”
BackgroundMitochondria-Associated Inflammasome Activation and Its Impact on Aging and Age-Related Diseases
Kauppinen, A. (2017) · Springer eBooks · doi:10.1007/978-3-319-64597-1_107-1 · Cited by 7
Watany, M. M., Elmazny, M. I., & Nasif, E. (2020) · Cytokine · doi:10.1016/j.cyto.2020.155102 · Cited by 6
PAIN AND INFLAMMATION. PART 1. PATHOGENETIC ASPECTS
Karateev, A. E., Karateev, D. E., & Давыдов, О. С. (2017) · Rheumatology Science and Practice · doi:10.14412/1995-4484-2016-693-704 · Cited by 7
Immune signalling by supramolecular assemblies
Kumar, S., & Jain, S. (2018) · Immunology · doi:10.1111/imm.12995 · Cited by 6
Mul1 suppresses Nlrp3 inflammasome activation through ubiquitination and degradation of AscPreprint
Kim, J., Lee, Y., Suh, G. Y., & Lee, Y. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/830380 · Cited by 6
“IL-1β and acting as a seed for new Asc speck formation after being engulfed by bystander macrophages [36, 37].”
BackgroundIqbal, O. (2023) · Medical Research Archives · doi:10.18103/mra.v12i1.4939 · Cited by 5
“The NLRP3 inflammasome works as a sensor of potential infection and toxicity and is important in the pathogenesis of different conditions 18,25–29 .”
BackgroundVCP Inhibition Augments NLRP3 Inflammasome Activation
Sharma, A., Dhavale, D. D., Kotzbauer, P. T., & Weihl, C. C. (2024) · Inflammation · doi:10.1007/s10753-024-02013-6 · Cited by 5
“Upon stimulation with the irritants, the NLRP3 inflammasome complex is assembled triggering the cleavage of CASPASE 1 to mediate the release of pro-inflammatory cytokine IL-1β and IL-18 in immune cells [1, 2].”
Lipid nanoparticle-delivered intrabodies for inhibiting necroptosis and pyroptosis
Deepagan, V. G., Ma, X., Bazregari, F., Pang, J., Schaefer, J., Hildebrand, J. M., Dempsey, R. K., Doerflinger, M., Baldwin, C. A., Schmidt, F. I., et al. (2025) · Biochemical Journal · doi:10.1042/bcj20253191 · Cited by 5
“Alternatively, or in addition, it may inhibit extracellular polymerized ASC specks that are released following cell lysis and can amplify inflammasome triggering through phagocytic uptake [39,40].”
Neuroinflammation and Neuroimmunomodulation in Alzheimer’s Disease
Hong, Y., Xu, J. L., Hu, Y., Li, L., Dong, Z., Zhu, T.-K., & Wei, Y.-Q. (2018) · Current Pharmacology Reports · doi:10.1007/s40495-018-0148-z · Cited by 6
Cambon, A., Rebelle, C., Bachelier, R., Arnaud, L., Robert, S., Lagarde, M., Muller, R., Tellier, E., Kara, Y., Leroyer, A. S., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1228122 · Cited by 5
Xiao, M., Zhang, P., Chen, Z., Liu, X., Wei, W., He, Z., Wang, Y., Cheng, J., Zhu, Z., Wen, J., et al. (2024) · Burns · doi:10.1016/j.burns.2024.01.009 · Cited by 5
Chiu, H., Wu, C., Lin, W., Wong, W.-T., Tsai, W.-C., Hsu, H.-T., Ho, C., Cheng, S., Cheng, C., Yang, S., et al. (2024) · Inflammation · doi:10.1007/s10753-023-01939-7 · Cited by 6
Alarcón‐Vila, C., Hurtado‐Navarro, L., Mateo, S. V., Peñín‐Franch, A., Martínez, C. M., Molina‐López, C., Baños, M. C., Gómez, A. I., Gómez‐Román, J., Baroja‐Mazo, A., et al. (2024) · EMBO Molecular Medicine · doi:10.1038/s44321-024-00176-1 · Cited by 4
Műzes, G., & Sípos, F. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26020598 · Cited by 5
Saha, D., Dutta, P., Rebello, K. R., Shankar, A., & Chakraborty, A. (2025) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-025-05236-9 · Cited by 5
“This interaction triggers inflammasome activation, leading to caspase-1-mediated cleavage of pro-IL-1β and pro-IL-18 into their active forms, intensifying vascular inflammation [102, 103].”
Alendronate Augments Lipid A–Induced IL-1α Release via Activation of ASC but Not Caspase-11
Tamai, R., Mashima, I., & Kiyoura, Y. (2021) · Inflammation · doi:10.1007/s10753-021-01489-w · Cited by 5
Sánchez, K. E., Bhaskar, K., & Rosenberg, G. A. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.976108 · Cited by 7
“IL-1β transcriptionally regulates MMPs, for example MMP13 and MMP9, in multiple cell types (Cheng et al., 2010; Hashimoto et al., 2013; Zhang et al., 2018; Sánchez and MaguireZeiss, 2020).”
BackgroundInfluentialZeng, N., Wang, Q., Zhang, C., Zhou, Y., & Yan, J. (2023) · Neurochemistry International · doi:10.1016/j.neuint.2023.105610 · Cited by 8
Chen, Y., Yang, L., Wang, C., & Wang, C. (2023) · Oncology Letters · doi:10.3892/ol.2023.14089 · Cited by 5
“IL‑1 β is produced in the form of a precursor peptide, which is cleaved and activated under the stimulation of PAMPs and DAMPs, and is a cellular stress response mechanism induced by invading pathogens and other danger signals, such as mycobacterium tuberculosis components (42,43).”
BackgroundRadic, M. Z. (2018) · Wiley eBooks · doi:10.1002/9781119432463.ch24 · Cited by 5
Ahmed, M. E., Suhail, H., Nematullah, M., Hoda, M. N., Giri, S., & Ahmad, A. S. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.25.600422 · Cited by 5
Visoso-Carvajal, G., García‐Cordero, J., Ybalmea-Gómez, Y., Díaz-Flores, M., León‐Juárez, M., Hernández‐Rivas, R., Nava, P., Villegas‐Sepúlveda, N., & Cedillo‐Barrón, L. (2025) · Pathogens · doi:10.3390/pathogens14121292 · Cited by 4
“NLRP3 functions as a molecular platform within innate immunity and is activated by viruses, such as DEN and Zika virus (ZIKV) [7,8].”
Pérez, D. C., Hernandez-Franco, J. F., & HogenEsch, H. (2026) · Scientific Reports · doi:10.1038/s41598-025-34660-6 · Cited by 4
“Previous studies have shown the release of specks from LPS-primed macrophages stimulated with ATP and nigericin 58,59 .”
Chakraborty, S., & Sinha, A. (2023) · Asian Journal of Pharmaceutical Research and Development · doi:10.22270/ajprd.v11i4.1302 · Cited by 4
“…also described that in Alzheimer's disease, activated astrocytes release proinflammatory cytokines like TNF-α, IL-6, IL-1, and TGF-β, which, in turn create decrease in ATP, and an increase in intracellular Ca2+, all of which contribute to neuroinflammation and worsening of cognitive function (53) .”
BackgroundLin, W.-Y., Tsui, J.-L., Chiu, H., Wong, W.-T., Wu, C., Hsu, H.-T., Ho, C., Yeh, S.-P., Rao, Y. K., Chen, A., et al. (2024) · BMC Infectious Diseases · doi:10.1186/s12879-024-10208-3 · Cited by 4
“Importantly, the extracellular release of inflammasome components from activated cells, especially those stemming from the NLRP3 inflammasome, has been shown to engage adjacent cells, thereby amplifying the inflammatory response [12].”
Cellular cross talk between epicardial fat and cardiovascular risk
Patel, V., & Patel, J. (2022) · Journal of Basic and Clinical Physiology and Pharmacology · doi:10.1515/jbcpp-2022-0230 · Cited by 6
Pyroptosis: A Promising Mechanism Linking SARS-CoV-2 Infection to Adverse Pregnancy Outcomes
Monti, P., Solazzo, G., Accurti, V., Gambitta, B., Iodice, S., Boito, S., Cantone, L., Manenti, A., Dioni, L., Montomoli, E., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119278 · Cited by 4
Gaspar-Morales, E. A., Waterston, A., Sadqi, M., Diaz-Parga, P., Smith, A. M., Gopinath, A., Eguiluz, R. C. A., & de Alba, E. (2023) · Biomacromolecules · doi:10.1021/acs.biomac.3c00409 · Cited by 4
Mateo, S. V., Vidal-Correoso, D., Muñoz-Morales, A. M., Jover-Aguilar, M., Alconchel, F., de la Peña, J., Martínez-Alarcón, L., López‐López, V., Ríos, A., Cascales-Campos, P. A., et al. (2024) · Cell Death Discovery · doi:10.1038/s41420-024-02042-y · Cited by 4
Hassen, M. D., Mousa, N. O., Radwan, S. M., & Gabre, R. M. (2025) · Inflammation · doi:10.1007/s10753-024-02187-z · Cited by 6
Hua, K., Chiu, H., Chen, M.-M., Wong, W.-T., Tsai, W., Lin, W.-Y., Wu, C., Wang, C.-C., Hsu, C.-H., Chernikov, O. V., et al. (2025) · Journal of Traditional and Complementary Medicine · doi:10.1016/j.jtcme.2025.06.003 · Cited by 4
“19 We found that NLRP3 and ASC were released from N. gonorrhoeae -infected macrophages, and while CA inhibited the release of NLRP3 (Fig.”
Nieman, D. C., Ferrara, F., Pecorelli, A., Woodby, B. L., Hoyle, A. T., Simonson, A. W., & Valacchi, G. (2020) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.2020-0084 · Cited by 4
Hernandez, C. A., & Eugenín, E. A. (2023) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2023.102404 · Cited by 4
Garbuzenko, D. V., & Belov, D. V. (2021) · Экспериментальная и клиническая гастроэнтерология · doi:10.31146/1682-8658-ecg-194-10-22-34 · Cited by 4
Inflammasome activators induce fibronectin expression and release in macrophages
Jun, H., Jung, Y.-J., & Choi, B. (2016) · Cellular Microbiology · doi:10.1111/cmi.12695 · Cited by 4
“As shown with other cytosolic components that are released via inflammasome stimuli‐induced pore formation (Baroja‐Mazo et al., 2014; Bergsbaken et al., 2011; Keller et al., 2008), Fn may be released in a similar manner.”
BackgroundInfluentialInflammasomes in Clinical Practice: A Brief Introduction
Alcocer‐Gómez, E., Castejón‐Vega, B., López-Sánchez, M., & Cordero, M. D. (2018) · Experientia supplementum · doi:10.1007/978-3-319-89390-7_1 · Cited by 4
Extracellular Caspase-1 regulates hair follicle stem cell migration during wound-healingPreprint
Ghosh, S., Hegde, A., Ananthan, A. S., Kataria, S., Pincha, N., Dutta, A., Dutta, A., Athreya, S., Khedkar, S. U., Dey, R., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/548529 · Cited by 4
Hu, B., Peng, X., Tang, C., Geng, M., Yao, S., Ai, J., & Ye, Y. (2024) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2024.107630 · Cited by 3
The PYRIN domain is required for TLR4-mediated inflammation by PYHIN family members
Iannucci, A., Lacarbonara, D., Caneparo, V., Castiglioni, F., Butticè, A., Raviola, S., Porta, C., Miggiano, R., Zanoni, I., Gariglio, M., et al. (2025) · iScience · doi:10.1016/j.isci.2025.112413 · Cited by 4
Demska, O., Szandruk-Bender, M., Bruun, N. E., Skov, V., Kjær, L., Larsen, M. K., Ellervik, C., Szmit, S., Hasselbalch, H. C., & Sobas, M. (2025) · Thrombosis and Haemostasis · doi:10.1055/a-2767-0451 · Cited by 3
Identifying the role of NLRP3 inflammasome in stroke progression and outcome before recanalization
Bellut, M., Kollikowski, A. M., Vogt, M. L., Roßnagel, L., Hawwari, I., Franklin, B. S., Pham, M., Stoll, G., & Schuhmann, M. K. (2026) · Cell Reports Medicine · doi:10.1016/j.xcrm.2026.102723 · Cited by 3
“16,19 This activation amplifies the inflammatory response and leads to the release of toxic molecules, such as neutrophil extracellular traps and matrix metalloproteinase-9, which damage the blood-brain barrier.”
NLRP3 Inflammasome Activation in Oxidative Stress: A Key Mechanism Driving Neuroinflammation
Ramirez-Celis, C., Martínez-Torres, A. M., & Morán, J. (2026) · NeuroImmunoModulation · doi:10.1159/000551943 · Cited by 3
Clinical Inflammasome Biomarkers: Progress and Prospects
Coombs, J. R., Burgener, S. S., & Schroder, K. (2026) · Journal of Molecular Biology · doi:10.1016/j.jmb.2026.169941 · Cited by 3
Akaho, R., Kiyoura, Y., & Tamai, R. (2024) · Journal of Oral Biosciences · doi:10.1016/j.job.2024.04.003 · Cited by 3
Ferroptosis in immune chaos: Unraveling its impact on disease and therapeutic potential
Direksunthorn, T., Ahmed, A. T., Pluetrattanabha, N., Uthirapathy, S., Ballal, S., Singh, A., Al‐Hetty, H. R. A. K., Devi, A., Sharma, G. C., & Yumashev, A. V. (2025) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-025-01078-7 · Cited by 4
“The main protein in charge of iron transportation is transferrin [6].”
Pang, H., Sun, X., Luo, S., Lin, J., Shi, X., Xiao, Y., Huang, G., Li, X., Xie, Z., & Zhou, Z. (2021) · Annals of Translational Medicine · doi:10.21037/atm-21-1126 · Cited by 2
“Accumulated evidence indicates that the inflammasome is involved in the development of autoimmune (8), inflammatory (9), and metabolic (10) diseases.”
BackgroundLi, L., Qiao, X., Ye, S., & Ke, Y. (2023) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-023-04378-0 · Cited by 3
“Any kind of hemorrhage activates a systematic inflammatory response [13] through secondary messengers, neutrophil activation, and changes in gene expression [14].”
BackgroundWong, W.-T., Li, L., Chiu, H., Menon, M. P., Hsu, H.-T., Lin, W., Wu, C., Ho, C., & Hua, K. (2024) · Journal of Traditional and Complementary Medicine · doi:10.1016/j.jtcme.2024.03.016 · Cited by 3
“25 We found that ATP induced the extracellular release of NLRP3 (Fig.”
Inflammasome-Driven Fatal Acute-on-Chronic Liver Failure Triggered by Mild COVID-19
Chen, V. C.-W., Joseph, C. R., Chan, W. O. Y., Sia, W. R., Su, Q., Sam, X. X., Tamilarasan, H., Mah, Y. Y., Ng, W. L., Yeong, J. P.-S., et al. (2024) · Viruses · doi:10.3390/v16101646 · Cited by 3
ASC-particle-induced Peritonitis
de Almeida, L., Dorfleutner, A., & Stehlik, C. (2016) · BIO-PROTOCOL · doi:10.21769/bioprotoc.1944 · Cited by 3
“Inflammasomes release not only cytokines, but also the polymeric ASC danger particles (pASC) by pyroptosis, which perpetuate and propagate inflammasome responses to bystander cells to engage cell intrinsic ASC and caspase-1 (Baroja-Mazo et al., 2014; Franklin et al., 2014).”
BackgroundMyeloid cell‐derived NLRP3 is dispensable for silica‐induced pulmonary inflammation and pathology
Barry, K. T., Harpur, C. M., Ambrose, R. L., Hodges, C. J., Mansell, A. S., Lam, M., & Tate, M. D. (2025) · Immunology and Cell Biology · doi:10.1111/imcb.70067 · Cited by 2
Wang, F., Xu, S., Wang, Q., Li, X., Jin, Q., Wang, L., Fu, A., & Li, W. (2025) · Food Science and Human Wellness · doi:10.26599/fshw.2025.9250487 · Cited by 2
Shared principles of human and bacterial antiviral immunity
Kranzusch, P. J. (2026) · Nature · doi:10.1038/s41586-026-10756-5 · Cited by 5
“…complex formation events may also be capable of driving extracellular responses in human antiviral immunity with aggregated ASC (apoptosis-associated speck-like protein containing a CARD) adapter protein ‘specks’ from dying cells phagocytosed to induce macrophage inflammasome activation 198,199 .”
RTN3 – ASC interaction: The potential mechanism behind diabetes-induced cortical neuritic dystrophy
Cheng, Q., & Zhang, M. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136333 · Cited by 2
Key Factors Regulating the Interdomain Dynamics May Contribute to the Assembly of ASC
Li, T., Pineda, L. I. G., Stevens, A. O., & He, Y. J. (2023) · Biology · doi:10.3390/biology12060796 · Cited by 2
Impact of ionizable groups in star polymer nanoparticles on NLRP3 inflammasome activation
Malhotra, M., Thodur, S. M., & Kulkarni, A. A. (2025) · Biomaterials Science · doi:10.1039/d4bm01349b · Cited by 2
Salaritabar, A., Darvish, B., Hadjiakhoondi, F., & Manayi, A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812491-8.00012-6 · Cited by 2
Inflammasomes and Autoinflammation
Broderick, L. (2019) · Springer eBooks · doi:10.1007/978-3-319-98605-0_5 · Cited by 2
ASC specks: a biomarker for myelodysplastic syndromes?
Wolf, D. G. F., & Latz, E. (2018) · The Lancet Haematology · doi:10.1016/s2352-3026(18)30113-3 · Cited by 2
Scambler, T., Jarosz-Griffiths, H., Reyna, S. J. L., Pathak, S., Wong, C. H., Holbrook, J. A., Martinon, F., Savic, S., Peckham, D. G., & McDermott, M. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/458208 · Cited by 2
Kugelberg, E. (2014) · Nature reviews. Immunology · doi:10.1038/nri3717 · Cited by 1
Korhonen, E. (2024) · Acta Ophthalmologica · doi:10.1111/aos.16646 · Cited by 2
Zhang, Q., Yu, S., Yang, Z., Wang, X., Li, J., Su, L., Zhang, H., Lou, X., Mao, H., Sun, Y., et al. (2024) · Biomedicines · doi:10.3390/biomedicines12122752 · Cited by 1
“NLRP3 can recognize pathogen-associated molecular patterns (PAMPs) and damage-associated molecular patterns (DAMPs), and it can promote the assembly of an inflammasome complex with the adaptor protein ASC and the effector protease caspase-1, which ultimately lead to pyroptosis [28,29].”
Shi, Y. P., Liu, A., & Li, X. (2025) · International Journal of Ophthalmology · doi:10.18240/ijo.2025.05.04 · Cited by 1
“NLRP3 inflammasome has the potency to sense soluble pathogen and danger-Figure associated molecular patterns, which is the central hub of the inflammatory response system that triggers pro-inflammatory responses [29] .”
Xiang, L., & Su, Z. (2025) · European journal of medical research · doi:10.1186/s40001-025-02927-3 · Cited by 3
“Also, macrophages in the surrounding area can engulf clusters of inflammasome molecules, which can further increase the intensity of the body’s inflammatory reaction [115].”
Mukherjee, B., Mallick, S., Bhattacharya, S., Ghosh, M. K., Roy, R., & Yadav, A. (2025) · Springer eBooks · doi:10.1007/978-981-96-8622-3_11 · Cited by 2
Salmonella-Induced Cell Death in Cancer Immunotherapy: What Lies Beneath?
Mónaco, A., Chilibroste, S., Plata, M. C., Chabalgoity, J. A., & Moreno, M. (2025) · Biomedicines · doi:10.3390/biomedicines14010012 · Cited by 1
“…cells also release alarmins such as ATP, HMGB1, and inflammasome complexes themselves; for example, oligomerized ASC “specks” are expelled from pyroptotic cells and can be phagocytosed by bystander macrophages to propagate Caspase-1 activation and cytokine release in the local environment [51].”
Ahmed, M. E., Suhail, H., Nematullah, M., Hoda, M. N., Giri, S., & Ahmad, A. S. (2026) · NeuroImmune Pharmacology and Therapeutics · doi:10.1515/nipt-2024-0019 · Cited by 6
TRIM21 facilitates inflammasome assembly and contributes to autoinflammatory disease
Carrière, J., Yun, C., Khare, S., Ismaeel, S., Jäger, E., Martins, V. D., Sims, K. A., Chu, L. H., Nguyen, H., de Almeida, L., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-73350-3 · Cited by 1
Bhagat, S., Kaur, K., Petronglo, J. R., O'Connor, L. D., Wang, C., Li, Y., Swarnkar, G., Khanna, K., Cassat, J. E., Novack, D. V., et al. (2026) · Infection and Immunity · doi:10.1128/iai.00200-26 · Cited by 1
“In addition, the possibility that ASC specks were released from inflammasome-activated cells and subsequently internalized by bystander cells cannot be excluded, as reported previously (45, 46).”
Mao, R., Liu, Y., Fan, Z., Li, Y., Yang, L., Xie, Q., Dong, H., Bi, M., Gao, C., Yang, Z., et al. (2026) · Cell Discovery · doi:10.1038/s41421-026-00898-1 · Cited by 1
Pyroptosis: Molecular mechanisms and function
Ajoolabady, A., Abdulkhaliq, A. A., Khan, J., Praticò, D., bahijri, S. M., Tuomilehto, J., Borai, A., Kim, B., & Ren, J. (2026) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-026-01210-1 · Cited by 1
Dual role of macrophage heterogeneity in allergic inflammation: from mechanism to targeted therapy
Yuan, G., Wang, M., Cao, Z., Wang, Y., & Gu, Z. (2026) · International Immunopharmacology · doi:10.1016/j.intimp.2026.117192 · Cited by 1
Particulate-Driven Type-2 Immunity and Allergic Responses
Kuroda, E., Temizoz, B., Coban, C., Ozasa, K., & Ishii, K. J. (2016) · Current topics in environmental health and preventive medicine · doi:10.1007/978-981-10-0351-6_5 · Cited by 1
The Role of Innate Immunity in Ischemic Stroke
Shichita, T., Ito, M., Morita, R., & Yoshimura, A. (2016) · Springer eBooks · doi:10.1007/978-4-431-56068-5_49 · Cited by 1
Zebrafish earns its stripes for in vivo ASC speck dynamics
Bezbradica, J. S., & Schroder, K. (2017) · The Journal of Cell Biology · doi:10.1083/jcb.201708002 · Cited by 1
“…by Kuri et al. (2017) is that the propagation of inflammasome activity in recipient macrophages as reported by the Pelegrin and Latz laboratories (Baroja-Mazo et al., 2014; Franklin et al., 2014) requires additional signals present in inflamed tissues (e.g., inflammatory regulators or high…”
InfluentialCurrent Opinion in the Treatment of Diabetic Nephropathy
Chen, X., Huang, C., & Pollock, C. A. (2015) · Nephrology - Open Journal · doi:10.17140/npoj-1-104
Role of Inflammasome Activation in Systemic Lupus Erythematosus: Are Innate Immune Cells Activated?
Pérez-Alamino, R., Cuchacovich, R., Espinoza, L. R., Porretta, C. P., & Zea, A. H. (2021) · Reumatología Clínica (English Edition) · doi:10.1016/j.reumae.2019.10.004 · Cited by 1
Inflammasome formation and triggers
Hafner‐Bratkovič, I. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-91802-2.00006-2 · Cited by 1
Mokia-Serbina, S. O., Litvіnova, T. V., Shelevytska, V., & Zabolotnia, N. I. (2024) · CHILD`S HEALTH · doi:10.22141/2224-0551.19.1.2024.1670 · Cited by 1
“Cruising together”—ASC specks and SAA, a perfect match in chronic inflammation
Maasewerd, S., & Franklin, B. S. (2024) · EMBO Molecular Medicine · doi:10.1038/s44321-024-00109-y · Cited by 1
“It took seven more years for the fi rst hypothesis to be proven correct (Baroja-Mazo et al, 2014; Franklin et al, 2014).”
BackgroundInfluential赵, 慧. (2024) · Journal of Clinical Personalized Medicine · doi:10.12677/jcpm.2024.34255 · Cited by 1
Insights into assembly of the macromolecular inflammasome complex
Monie, T. P., & Boyle, J. P. (2014) · Inflammasome · doi:10.2478/infl-2014-0009 · Cited by 1
The nature of the immune response in microbial-associated and sterile intraamniotic inflammation
Gomez‐Lopez, N., & Romero, R. J. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-818508-7.00003-8 · Cited by 1
Pharmacological Inhibition of BTK reduces neuroinflammation and stress induced anxiety in vivoPreprint
Ghosh, S., Mohammed, Z., & Singh, I. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.11.426241 · Cited by 1
“widely in the central nervous system and cells of myeloid lineage (Martinon et al., 2002; Agostini et al., 2004; Baroja-Mazo et al., 2014; Guo et al., 2015; Schroder and Tschopp, 2010).”
BackgroundLawlor, K. E., Conos, S. A., & Vince, J. E. (2018) · Wiley eBooks · doi:10.1002/9781119432463.ch15 · Cited by 1
Vega, M. T. M., Matilla, J., Bazán, E., Reimers, D., de Andrés-Martín, A., Gonzalo‐Gobernado, R., Corrêa, C., Urbano, F., & Gómez‐Coronado, D. (2023) · Preprints.org · doi:10.20944/preprints202311.1488.v1 · Cited by 1
Pedoto, A., Lozano‐Gil, J. M., Chi, M. N., Lutfalla, G., García‐Moreno, D., Cayuela, M. L., Tyrkalska, S. D., & Mulero, V. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.22.634381 · Cited by 1
Välimäki, E. (2015) · Työväentutkimus Vuosikirja
NLRP3 Inflammasome-Mediated Toxicity of Fibrous Particles
Kanno, S. (2016) · Current topics in environmental health and preventive medicine · doi:10.1007/978-4-431-55732-6_2
Role of the inflammasome pathway in atherosclerosis
Rajamäki, K. (2015) · Työväentutkimus Vuosikirja
NAIP and CARD-only proteins in inflammasome signaling
Matusiak, M. (2015) · Ghent University Academic Bibliography (Ghent University)
Metadata
- Authors
- Baroja-Mazo, A., Martín-Sánchez, F., Gomez, A. I., Martínez, C. M., Amores-Iniesta, J., Compan, V., Barberà-Cremades, M., Yagüe, J., Ruiz-Ortiz, E., Antón, J., Buján, S., Couillin, I., Brough, D., Arostegui, J. I., & Pelegrín, P.
- Affiliations
- Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (ES)
- University of Manchester (GB)
- Hospital Clínic de Barcelona (ES)
- Hospital Sant Joan de Déu Barcelona (ES)
- Vall d'Hebron Hospital Universitari (ES)
- Université d'Orléans (FR)
- ORCID
- Venue
- Nature Immunology
- Published
- 2014-06-22
- Volume
- 15
- Issue
- 8
- Pages
- 738-748
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- OpenAlex
- W2143119237
- Cited by
- 790
- References
- 50
- Citations by year
- 2026: 28 · 2025: 39 · 2024: 41 · 2023: 63 · 2022: 81 · 2021: 84 · 2020: 86 · 2019: 68 · 2018: 74 · 2017: 88 · 2016: 60 · 2015: 57 · 2014: 20
- FWCI
- 30.77
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Licence
- cc-by-nc-nd
- www.springer.com/tdm (tdm)
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- Hispana (publishedVersion, cc-by-nc-nd)
- Research Explorer (The University of Manchester) (submittedVersion)
- Funders
- Wellcome Trust
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Health Sciences › Medicine › Hematology › Autoimmune and Inflammatory Disorders Research
- Keywords
- NLRP3 inflammasome, caspase-1, IL-1β processing, cryopyrin-associated periodic syndromes, macrophages, autoinflammatory disease, phagocytosis
- MeSH terms
- NLR Family, Pyrin Domain-Containing 3 Protein, Animals, Carrier Proteins, Cells, Cultured, Cytoskeletal Proteins, Humans, Inflammation, Macrophages, Mice, Inbred C57BL, Phagocytosis, Signal Transduction, Mice, Knockout, Caspases, Caspase 1, Apoptosis Regulatory Proteins, Mice, CARD Signaling Adaptor Proteins, Caspases, Initiator, Interleukin-1beta, Cryopyrin-Associated Periodic Syndromes, HEK293 Cells, Inflammasomes
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