Metabolic regulation of NLRP 3
Open accessAbstract
Summary: A shift in our understanding of macrophage biology has come about as a result of recent discoveries in the area of metabolic reprogramming of macrophages. The NLRP 3 inflammasome drives the activation of caspase‐1, leading to the production of IL ‐1β, IL ‐18, and a type of cell death termed pyroptosis. The NLRP 3 inflammasome has been shown to sense metabolites such as palmitate, uric acid, and cholesterol crystals and is inhibited by ketone bodies produced during metabolic flux. The NLRP 3 inflammasome has also been shown to be regulated by mitochondrial reactive oxygen species and components of glycolysis, such as Hexokinase. Here, we review these findings and discuss their importance for inflammation and furthermore discuss potential therapeutic benefits of targeting NLRP 3.
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
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?
A number of molecules in lipid metabolism pathways have been identified to regulate NLRP3 inflammasome activation.
“A number of molecules in lipid metabolism pathways have been identified to regulate NLRP3 inflammasome activation [41].”
From HIV-TAT dysregulates microglial lipid metabolism through SREBP2/miR-124 axis: Implication of lipid droplet accumulation microglia in NeuroHIV (2025) · cites this paper as [41]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
3 retracted
RETRACTED: mTORC1-Induced HK1-Dependent Glycolysis Regulates NLRP3 Inflammasome Activation
Moon, J.-S., Hisata, S., Park, M. A., DeNicola, G. M., Ryter, S. W., Nakahira, K., & Choi, A. M. K. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.05.046 · Cited by 370 · see citing works
RetractedMoon, J.-S., Nakahira, K., Chung, K.-P., DeNicola, G. M., Koo, M. J., Pabón, M. A., Rooney, K. T., Yoon, J.-H., Ryter, S. W., Stout-Delgado, H., et al. (2016) · Nature Medicine · doi:10.1038/nm.4153 · Cited by 291 · see citing works
RetractedUCP2-induced fatty acid synthase promotes NLRP3 inflammasome activation during sepsis
Moon, J.-S., Lee, S., Park, M.-A., Siempos, I. I., Haslip, M., Lee, P. J., Yun, M., Kim, C. K., Howrylak, J., Ryter, S. W., et al. (2015) · Journal of Clinical Investigation · doi:10.1172/jci78253 · Cited by 238 · see citing works
RetractedMartinon, F., Burns, K., & Tschopp, J. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00599-3 · Cited by 6,066 · see citing works
A role for mitochondria in nlrp3 inflammasome activation
Zhou, R., Yazdi, A. S., Menu, P., & Tschopp, J. (2011) · Nature · doi:10.1038/nature09663 · Cited by 5,602 · see citing works
Succinate is an inflammatory signal that induces IL-1β through HIF-1α
Tannahill, G. M., Curtis, A. M., Adamik, J., Palsson-McDermott, E. M., McGettrick, A. F., Goel, G., Frezza, C., Bernard, N. J., Kelly, B., Foley, N. H., et al. (2013) · Nature · doi:10.1038/nature11986 · Cited by 4,176 · see citing works
Self-citationCaspase-11 cleaves gasdermin D for non-canonical inflammasome signalling
Kayagaki, N., Stowe, I. B., Lee, B. L., O’Rourke, K., Anderson, K., Warming, S., Cuellar, T., Haley, B., Roose-Girma, M., Phung, Q. T., et al. (2015) · Nature · doi:10.1038/nature15541 · Cited by 3,686 · see citing works
Mitochondria: In Sickness and in Health
Nunnari, J., & Suomalainen, A. (2012) · Cell · doi:10.1016/j.cell.2012.02.035 · Cited by 3,479 · see citing works
A small-molecule inhibitor of the NLRP3 inflammasome for the treatment of inflammatory diseases
Coll, R. C., Robertson, A. A. B., Chae, J. J., Higgins, S. C., Muñoz-Planillo, R., Inserra, M. C., Vetter, I., Dungan, L. S., Monks, B. G., Stutz, A., et al. (2015) · Nature Medicine · doi:10.1038/nm.3806 · Cited by 2,849 · see citing works
Self-citationThioredoxin-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 · see citing works
Innate Immune Activation Through Nalp3 Inflammasome Sensing of Asbestos and Silica
Dostert, C., Pétrilli, V., Van Bruggen, R., Steele, C., Mossman, B. T., & Tschopp, J. (2008) · Science · doi:10.1126/science.1156995 · Cited by 2,658 · see citing works
The NLRP3 inflammasome instigates obesity-induced inflammation and insulin resistance
Vandanmagsar, B., Youm, Y.-H., Ravussin, A., Galgani, J. E., Stadler, K., Mynatt, R. L., Ravussin, E., Stephens, J. M., & Dixit, V. D. (2011) · Nature Medicine · doi:10.1038/nm.2279 · Cited by 2,655 · see citing works
Non-canonical inflammasome activation targets caspase-11
Kayagaki, N., Warming, S., Lamkanfi, M., Walle, L. V., Louie, S., Dong, J., Newton, K., Qu, Y., Liu, J., Heldens, S., et al. (2011) · Nature · doi:10.1038/nature10558 · Cited by 2,530 · see citing works
Mills, E. L., Kelly, B., Logan, A., Costa, A. S. H., Varma, M., Bryant, C. E., Tourlomousis, P., Däbritz, J. H. M., Gottlieb, E., Latorre, I., et al. (2016) · Cell · doi:10.1016/j.cell.2016.08.064 · Cited by 2,291 · see citing works
Self-citationOxidized mitochondrial DNA activates the NLRP3 inflammasome during apoptosis
Shimada, K., Crother, T. R., Karlin, J., Dagvadorj, J., Chiba, N., Chen, S., Ramanujan, V. K., Wolf, A. J., Vergnes, L., Ojcius, D. M., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.01.009 · Cited by 2,282 · see citing works
The ketone metabolite β-hydroxybutyrate blocks NLRP3 inflammasome-mediated inflammatory disease
Youm, Y.-H., Nguyen, K. Y., Grant, R. W., Goldberg, E. L., Bodogai, M., Kim, D., D'Agostino, D., Planavsky, N., Lupfer, C., Kanneganti, T. D., et al. (2015) · Nature Medicine · doi:10.1038/nm.3804 · Cited by 2,172 · see citing works
Muñoz-Planillo, R., Kuffa, P., Martínez-Colón, G. J., Smith, B. L., Rajendiran, T. M., & Núñez, G. (2013) · Immunity · doi:10.1016/j.immuni.2013.05.016 · Cited by 2,167 · see citing works
Cellular mechanisms and physiological consequences of redox-dependent signalling
Holmström, K. M., & Finkel, T. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3801 · Cited by 2,093 · see citing works
Fatty acid–induced NLRP3-ASC inflammasome activation interferes with insulin signaling
Wen, H., Gris, D., Lei, Y. L., Jha, S., Zhang, L., Huang, M. T.-H., Brickey, W. J., & Ting, J. P. ‐. (2011) · Nature Immunology · doi:10.1038/ni.2022 · Cited by 1,811 · see citing works
Agostini, L., Martinon, F., Burns, K., McDermott, M. F., Hawkins, P. N., & Tschopp, J. (2004) · Immunity · doi:10.1016/s1074-7613(04)00046-9 · Cited by 1,768 · see citing works
Lampropoulou, V., Sergushichev, A., Bambousková, M., Nair, S., Vincent, E. E., Loginicheva, E., Cervantes‐Barragán, L., Ma, X., Huang, S. C., Griss, T., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.06.004 · Cited by 1,547 · see citing works
Pyruvate Kinase M2 Is a PHD3-Stimulated Coactivator for Hypoxia-Inducible Factor 1
Luo, W., Hu, H., Chang, R., Zhong, J., Knabel, M., O'Meally, R., Cole, R. N., Pandey, A., & Semenza, G. L. (2011) · Cell · doi:10.1016/j.cell.2011.03.054 · Cited by 1,463 · see citing works
Palsson-McDermott, E. M., Curtis, A. M., Goel, G., Lauterbach, M. A. R., Sheedy, F. J., Gleeson, L. E., van den Bosch, M. W. M., Quinn, S. R., Domingo-Fernandez, R., Johnston, D. G. W., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2014.12.005 · Cited by 1,397 · see citing works
Self-citationAnti-inflammatory effect of IL-10 mediated by metabolic reprogramming of macrophages
Ip, W., Hoshi, N., Shouval, D. S., Snapper, S. B., & Medzhitov, R. M. (2017) · Science · doi:10.1126/science.aal3535 · Cited by 1,382 · see citing works
Unified Polymerization Mechanism for the Assembly of ASC-Dependent Inflammasomes
Lu, A., Magupalli, V. G., Ruan, J., Yin, Q., Atianand, M. K., Vos, M. R., Schröder, G. F., Fitzgerald, K. A., Wu, H., & Egelman, E. H. (2014) · Cell · doi:10.1016/j.cell.2014.02.008 · Cited by 1,353 · see citing works
NEK7 is an essential mediator of NLRP3 activation downstream of potassium efflux
He, Y., Zeng, M. Y., Yang, D., Motro, B., & Núñez, G. (2016) · Nature · doi:10.1038/nature16959 · Cited by 1,295 · see citing works
The NLRC4 inflammasome receptors for bacterial flagellin and type III secretion apparatus
Zhao, Y., Yang, J., Shi, J., Gong, Y., Lu, Q., Xu, H., Liu, L., & Shao, F. (2011) · Nature · doi:10.1038/nature10510 · Cited by 1,273 · see citing works
Mitochondrial Cardiolipin Is Required for Nlrp3 Inflammasome Activation
Iyer, S. S., He, Q., Janczy, J. R., Elliott, E. I., Zhong, Z., Olivier, A. K., Sadler, J. J., Knepper-Adrian, V., Han, R., Qiao, L., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.08.001 · Cited by 939 · see citing works
Human Monocytes Engage an Alternative Inflammasome Pathway
Gaidt, M. M., Ebert, T. S., Chauhan, D., Schmidt, T., Schmid-Burgk, J. L., Rapino, F. A., Robertson, A. A. B., Cooper, M. A., Graf, T., & Hornung, V. (2016) · Immunity · doi:10.1016/j.immuni.2016.01.012 · Cited by 780 · see citing works
Shi, H., Wang, Y., Li, X., Zhan, X., Tang, M., Fina, M., Su, L., Pratt, D., Bu, C. H., Hildebrand, S., et al. (2015) · Nature Immunology · doi:10.1038/ni.3333 · Cited by 751 · see citing works
Inflammasome is a central player in the induction of obesity and insulin resistance
Stienstra, R., van Diepen, J. A., Tack, C. J., Zaki, M. H., van de Veerdonk, F. L., Perera, D., Neale, G. A., Hooiveld, G. J., Hijmans, A., Vroegrijk, I., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1100255108 · Cited by 727 · see citing works
Canonical Nlrp3 Inflammasome Links Systemic Low-Grade Inflammation to Functional Decline in Aging
Youm, Y.-H., Grant, R. W., McCabe, L. R., Albarado, D. C., Nguyen, K. Y., Ravussin, A., Pistell, P., Newman, S., Carter, R., Laque, A., et al. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.09.010 · Cited by 674 · see citing works
Majewski, N., Nogueira, V., Bhaskar, P. T., Coy, P. E., Skeen, J. E., Gottlob, K., Chandel, N. S., Thompson, C. B., Robey, R. B., & Hay, N. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.11.014 · Cited by 633 · see citing works
The inflammation highway: metabolism accelerates inflammatory traffic in obesity
Johnson, A. R., Justin Milner, J., & Makowski, L. (2012) · Immunological Reviews · doi:10.1111/j.1600-065x.2012.01151.x · Cited by 603 · see citing works
Heid, M. E., Keyel, P. A., Kamga, C., Shiva, S., Watkins, S. C., & Salter, R. D. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1301490 · Cited by 570 · see citing works
PKM2-dependent glycolysis promotes NLRP3 and AIM2 inflammasome activation
Xie, M., Yu, Y., Kang, R., Zhu, S., Yang, L., Zeng, L., Sun, X., Yang, M., Billiar, T. R., Wang, H., et al. (2016) · Nature Communications · doi:10.1038/ncomms13280 · Cited by 567 · see citing works
Hexokinase Is an Innate Immune Receptor for the Detection of Bacterial Peptidoglycan
Wolf, A. J., Reyes, C. N., Liang, W., Becker, C. A., Shimada, K., Wheeler, M. L., Cho, H. C., Popescu, N. I., Coggeshall, K. M., Arditi, M., et al. (2016) · Cell · doi:10.1016/j.cell.2016.05.076 · Cited by 554 · see citing works
Regulation of bile acid synthesis: pathways, nuclear receptors, and mechanisms
Chiang, J. Y. L. (2003) · Journal of Hepatology · doi:10.1016/j.jhep.2003.11.006 · Cited by 550 · see citing works
Redundant roles for inflammasome receptors NLRP3 and NLRC4 in host defense against <i>Salmonella</i>
Broz, P., Newton, K., Lamkanfi, M., Mariathasan, S., Dixit, V. M., & Monack, D. M. (2010) · Journal of Experimental Medicine · doi:10.1084/jem.20100257 · Cited by 549 · see citing works
Akt activates the mammalian target of rapamycin by regulating cellular ATP level and AMPK activity
Hahn-Windgassen, A., Nogueira, V., Chen, C.-C., Skeen, J. E., Sonenberg, N., & Hay, N. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m502876200 · Cited by 539 · see citing works
K + Efflux-Independent NLRP3 Inflammasome Activation by Small Molecules Targeting Mitochondria
Groß, C. J., Mishra, R., Schneider, K. S., Médard, G., Wettmarshausen, J., Dittlein, D., Shi, H., Gorka, O., Koenig, P.-A., Fromm, S., et al. (2016) · Immunity · doi:10.1016/j.immuni.2016.08.010 · Cited by 530 · see citing works
Inflammasome activation leads to Caspase-1–dependent mitochondrial damage and block of mitophagy
Yu, J.-J., Nagasu, H., Murakami, T., Hoang, H., Broderick, L., Hoffman, H., & Horng, T. (2014) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1414859111 · Cited by 449 · see citing works
Inflammaging and Anti-Inflammaging: The Role of Cytokines in Extreme Longevity
Minciullo, P. L., Catalano, A., Mandraffino, G., Casciaro, M., Crucitti, A., Maltese, G., Morabito, N., Lasco, A., Gangemi, S., & Basile, G. (2016) · Archivum Immunologiae et Therapiae Experimentalis · doi:10.1007/s00005-015-0377-3 · Cited by 433 · see citing works
β-hydroxybutyrate deactivates neutrophil NLRP3 inflammasome to relieve gout flares
Goldberg, E. L., Asher, J. L., Molony, R. D., Shaw, A. C., Zeiss, C. J., Wang, C., Morozova-Roche, L. A., Herzog, R. I., Iwasaki, A., & Dixit, V. D. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.02.004 · Cited by 370 · see citing works
Tang, T., Lang, X., Xu, C., Wang, X., Gong, T., Yang, Y., Cui, J., Bai, L., Wang, J., Jiang, W., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00227-x · Cited by 364 · see citing works
Pasinelli, P., Houseweart, M. K., Brown, R. H., & Cleveland, D. W. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.240305897 · Cited by 344 · see citing works
Kelly, B., Tannahill, G. M., Murphy, M. P., & O'Neill, L. A. J. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.662114 · Cited by 334 · see citing works
Self-citationClarke, K., Tchabanenko, K., Pawlosky, R., Carter, E., Todd King, M., Musa-Veloso, K., Ho, M., Roberts, A., Robertson, J., VanItallie, T. B., et al. (2012) · Regulatory Toxicology and Pharmacology · doi:10.1016/j.yrtph.2012.04.008 · Cited by 332 · see citing works
Role of IL-1β in type 2 diabetes
Dinarello, C. A., Donath, M. Y., & Mandrup-Poulsen, T. R. (2010) · Current Opinion in Endocrinology Diabetes and Obesity · doi:10.1097/med.0b013e32833bf6dc · Cited by 330 · see citing works
Shao, W., Yeretssian, G., Doiron, K., Hussain, S. N. A., & Saleh, M. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m708182200 · Cited by 321 · see citing works
Superoxide dismutase 1 regulates caspase-1 and endotoxic shock
Meissner, F., Molawi, K., & Zychlinsky, A. (2008) · Nature Immunology · doi:10.1038/ni.1633 · Cited by 302 · see citing works
Park, S., Juliana, C. A., Hong, S., Datta, P., Hwang, I., Fernandes‐Alnemri, T., Yu, J., & Alnemri, E. S. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1301170 · Cited by 266 · see citing works
Yamanashi, T., Iwata, M., Kamiya, N., Tsunetomi, K., Kajitani, N., Wada, N., Iitsuka, T., Yamauchi, T., Miura, A., Pu, S., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-08055-1 · Cited by 214 · see citing works
The interplay between inflammation and metabolism in rheumatoid arthritis
Chimenti, M. S., Triggianese, P., Conigliaro, P., Candi, E., Melino, G., & Perricone, R. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.246 · Cited by 208 · see citing works
Disruption of glycolytic flux is a signal for inflammasome signaling and pyroptotic cell death
Sanman, L. E., Yu, Q., Eisele, N. A., Ng, T. M., van der Linden, W. A., Monack, D. M., Weerapana, E., & Bogyo, M. S. (2016) · eLife · doi:10.7554/elife.13663 · Cited by 193 · see citing works
Bile Acids Control Inflammation and Metabolic Disorder through Inhibition of NLRP3 Inflammasome
Guo, C., Xie, S., Chi, Z., Zhang, J., Liu, Y., Zhang, L., Zheng, M., Zhang, X., Xia, D., Ke, Y., et al. (2016) · Immunity · doi:10.1016/j.immuni.2016.10.009 · Cited by 175 · see citing works
Reversible Cysteine Oxidation in Hydrogen Peroxide Sensing and Signal Transduction
García‐Santamarina, S., Boronat, S., & Hidalgo, E. (2014) · Biochemistry · doi:10.1021/bi401700f · Cited by 174 · see citing works
Sokołowska, M., Chen, L., Liu, Y., Martínez‐Antón, A., Qi, H., Logun, C., Alsaaty, S., Park, Y. H., Kastner, D. L., Chae, J. J., et al. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1401343 · Cited by 169 · see citing works
Domingo-Fernandéz, R., Coll, R. C., Kearney, J., Breit, S. N., & O'Neill, L. A. J. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.797126 · Cited by 167 · see citing works
Self-citationLee, J. (2013) · Archives of Pharmacal Research · doi:10.1007/s12272-013-0023-8 · Cited by 157 · see citing works
Liu, X., Zhou, W., Zhang, X., Lü, P., Du, Q., Tao, L., Ding, Y., Wang, Y., & Hu, R. (2016) · Biochemical Pharmacology · doi:10.1016/j.bcp.2016.05.002 · Cited by 146 · see citing works
Qin, Y., Li, M., Feng, X., Wang, J., Cao, L., Shen, X.-K., Chen, J., Sun, M., Sheng, R., Han, F., et al. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.01.034 · Cited by 137 · see citing works
Flagellin-induced NLRC4 phosphorylation primes the inflammasome for activation by NAIP5
Matusiak, M., Opdenbosch, N. V., Walle, L. V., Sirard, J., Kanneganti, T., & Lamkanfi, M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1417945112 · Cited by 129 · see citing works
Feng, H., Gu, J., Gou, F., Huang, W. G., Gao, C., Chen, G., Long, Y., Zhou, X., Yang, M., Liu, S., et al. (2016) · Journal of Diabetes Research · doi:10.1155/2016/6973175 · Cited by 128 · see citing works
Inhibition of caspase-3 activity and activation by protein glutathionylation
Huang, Z., Pinto, J. T., Deng, H., & Richie, J. P. (2008) · Biochemical Pharmacology · doi:10.1016/j.bcp.2008.02.026 · Cited by 125 · see citing works
Kong, G., Huang, Z., Ji, W., Wang, X., Liu, J., Wu, X., Huang, Z., Li, R., & Zhu, Q. (2017) · Journal of Neurotrauma · doi:10.1089/neu.2017.5192 · Cited by 113 · see citing works
Li, Y., Zheng, J., Liu, J., Yang, J., Liu, Y., Wang, C., Ma, X., Liu, B., Xin, G.-Z., & Liu, L. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00532 · Cited by 110 · see citing works
Innate Immune System Cells in Atherosclerosis
Chávez-Sanchéz, L., Espinosa-Luna, J. E., Chávez-Rueda, A. K., Legorreta-Haquet, M. V., Montoya-Díaz, E., & Blanco-Favela, F. A. (2013) · Archives of Medical Research · doi:10.1016/j.arcmed.2013.11.007 · Cited by 106 · see citing works
Oxidative metabolism enables Salmonella evasion of the NLRP3 inflammasome
Wynosky-Dolfi, M. A., Snyder, A. G., Philip, N. H., Doonan, P. J., Poffenberger, M. C., Avizonis, D. Z., Zwack, E. E., Riblett, A. M., Hu, B., Strowig, T., et al. (2014) · The Journal of Experimental Medicine · doi:10.1084/jem.20130627 · Cited by 104 · see citing works
The NLRP3 inflammasome contributes to sarcopenia and lower muscle glycolytic potential in old mice
McBride, M. J., Foley, K. P., D’Souza, D. M., Li, Y. E., Lau, T. C., Hawke, T. J., & Schertzer, J. D. (2017) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00060.2017 · Cited by 99 · see citing works
Nlrp3 is a key modulator of diet-induced nephropathy and renal cholesterol accumulation
Bakker, P. J., Butter, L. M., Kors, L., Teske, G. J. D., Aten, J., Sutterwala, F. S., Florquin, S., & Leemans, J. C. (2013) · Kidney International · doi:10.1038/ki.2013.503 · Cited by 98 · see citing works
The Induction of Pro–IL-1β by Lipopolysaccharide Requires Endogenous Prostaglandin E2 Production
Zasłona, Z., Pålsson‐McDermott, E. M., Menon, D., Haneklaus, M., Flis, E., Prendeville, H., Corcoran, S. E., Peters-Golden, M. L., & O'Neill, L. A. J. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1602072 · Cited by 94 · see citing works
Self-citationTseng, H. H. L., Vong, C. T., Kwan, Y. W., Lee, S. M., & Hoi, M. P. M. (2016) · Scientific Reports · doi:10.1038/srep35016 · Cited by 85 · see citing works
Cunha, L. D., Silva, A. L. N., Ribeiro, J. M., Mascarenhas, D. P. A., Quirino, G. F. S., dos Santos, L. L., Flavell, R. A., & Zamboni, D. S. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.06.086 · Cited by 84 · see citing works
Nomura, J., So, A. K.-L., Tamura, M., & Busso, N. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402512 · Cited by 79 · see citing works
Lima-Junior, D. S., Mineo, T. W. P., Calich, V. L. G., & Zamboni, D. S. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1700258 · Cited by 71 · see citing works
Sulfonylureas as Concomitant Insulin Secretagogues and NLRP3 Inflammasome Inhibitors
Hill, J. R., Coll, R. C., Sue, N., Reid, J. C., Dou, J., Holley, C. L., Pelingon, R., Dickinson, J. B., Biden, T. J., Schroder, K., et al. (2017) · ChemMedChem · doi:10.1002/cmdc.201700270 · Cited by 65 · see citing works
Haneklaus, M., O’Neil, J. D., Clark, A. R., Masters, S. L., & O'Neill, L. A. J. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.772947 · Cited by 65 · see citing works
Self-citationGuglielmo, A., Sabra, A., Elbery, M., Cerveira, M. M., Ghenov, F., Sunasee, R., & Ckless, K. (2017) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2017.06.028 · Cited by 43 · see citing works
Wang, C., Xu, C., Alippe, Y., Qu, C., Xiao, J., Schipani, E., Civitelli, R., Abu‐Amer, Y., & Mbalaviele, G. (2017) · Scientific Reports · doi:10.1038/s41598-017-05033-5 · Cited by 35 · see citing works
A novel immunomodulatory effect of ugonin U in human neutrophils via stimulation of phospholipase C
Chen, C., Liaw, C., Chen, Y., Chang, W.-Y., Chung, P.-J., & Hwang, T. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.04.018 · Cited by 34 · see citing works
Chen, C., Yang, C.-H., Tsai, Y., Liaw, C., Chang, W.-Y., & Hwang, T. (2016) · Redox Biology · doi:10.1016/j.redox.2016.12.018 · Cited by 33 · see citing works
Hughes, M. M., Lavrencic, P., Coll, R. C., Ve, T., Ryan, D. G., Williams, N. C., Menon, D., Mansell, A. S., Philip G. Board, Mobli, M., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1701868114 · Cited by 33 · see citing works
Self-citationCysteine Oxidation Enhanced by Iron in Tristetraprolin, A Zinc Finger Peptide
Lee, S. J., & Michel, S. L. J. (2010) · Inorganic Chemistry · doi:10.1021/ic9024298 · Cited by 28 · see citing works
Glutathione and Glutathione Transferase Omega 1 as Key Posttranslational Regulators in Macrophages
Hughes, M. M., McGettrick, A. F., & O'Neill, L. A. J. (2017) · Microbiology Spectrum · doi:10.1128/microbiolspec.mchd-0044-2016 · Cited by 27 · see citing works
Self-citationKemper, M. F., Srivastava, S., King, M. T., Clarke, K., Veech, R. L., & Pawlosky, R. J. (2015) · Lipids · doi:10.1007/s11745-015-4085-x · Cited by 26 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- 1600065x, 2018, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/imr.12608 by Mount Vernon Nazarene University, Wiley Online Library on [14/01/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License | 97 · DOI
- Pasinelli P. Caspase-1 and -3 are sequentially activated in motor neu- ron death. Proc Natl Acad Sci U S A. 2000;97:13901-13906.
Cited by
Sorted by citations
The NLRP3 inflammasome: molecular activation and regulation to therapeutics
Swanson, K. V., Deng, M., & Ting, J. P.-Y. (2019) · Nature Reviews Immunology · doi:10.1038/s41577-019-0165-0 · Cited by 4,884 · see citing works
Recent advances in the mechanisms of NLRP3 inflammasome activation and its inhibitors
Yang, Y., Wang, H., Kouadir, M., Song, H., & Shi, F. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1413-8 · Cited by 1,285 · see citing works
Reactive Oxygen Species: Drivers of Physiological and Pathological Processes
Checa, J., & Aran, J. M. (2020) · Journal of Inflammation Research · doi:10.2147/jir.s275595 · Cited by 1,022 · see citing works
Interleukin-18 in Health and Disease
Yasuda, K., Nakanishi, K., & Tsutsui, H. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20030649 · Cited by 564 · see citing works
A 360° view of the inflammasome: Mechanisms of activation, cell death, and diseases
Barnett, K. C., Li, S., Liang, K., & Ting, J. P.-Y. (2023) · Cell · doi:10.1016/j.cell.2023.04.025 · Cited by 458 · see citing works
Dopamine, Immunity, and Disease
Channer, B., Matt, S. M., Nickoloff-Bybel, E. A., Pappa, V., Agarwal, Y., Wickman, J. R., & Gaskill, P. J. (2022) · Pharmacological Reviews · doi:10.1124/pharmrev.122.000618 · Cited by 319 · see citing works
PANoptosis : Mechanisms, biology, and role in disease
Sun, X., Yang, Y., Meng, X., Li, J., Liu, X., & Liu, H. (2023) · Immunological Reviews · doi:10.1111/imr.13279 · Cited by 314 · see citing works
Bonnet, F., & Scheen, A. J. (2018) · Diabetes & Metabolism · doi:10.1016/j.diabet.2018.09.005 · Cited by 311 · see citing works
Intracellular and Intercellular Aspects of Macrophage Immunometabolism in Atherosclerosis
Tabas, I. A., & Bornfeldt, K. (2020) · Circulation Research · doi:10.1161/circresaha.119.315939 · Cited by 249 · see citing works
Ma, Q. (2023) · Pharmacological Reviews · doi:10.1124/pharmrev.122.000629 · Cited by 256 · see citing works
NLRP3 inflammasome priming: A riddle wrapped in a mystery inside an enigma
McKee, C. M., & Coll, R. C. (2020) · Journal of Leukocyte Biology · doi:10.1002/jlb.3mr0720-513r · Cited by 236 · see citing works
Programmed cell death in atherosclerosis and vascular calcification
Li, M., Wang, Z., Fang, L., Cheng, S.-Q., Wang, X., & Liu, N. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-04923-5 · Cited by 229 · see citing works
Inhibition of glycolysis alleviates lipopolysaccharide‐induced acute lung injury in a mouse model
Zhong, W., Yang, H., Guan, X., Xiong, J., Sun, C., Zhang, C., Luo, X., Zhang, Y., Zhang, J., Duan, J., et al. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27261 · Cited by 216 · see citing works
The NLRP3 Inflammasome: Metabolic Regulation and Contribution to Inflammaging
Meyers, A. K., & Zhu, X. (2020) · Cells · doi:10.3390/cells9081808 · Cited by 203 · see citing works
Yu, H., Chang, Q., Sun, T., He, X., Wen, L., An, J., Feng, J., & Zhao, Y. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.102032 · Cited by 208 · see citing works
Zhang, X., Wang, R., Hu, D., Sun, X., Fujioka, H., Lundberg, K., Chan, E. R., Wang, Q., Xu, R., Flanagan, M. E., et al. (2020) · Science Advances · doi:10.1126/sciadv.abb8680 · Cited by 200 · see citing works
Punicalagin Protects Diabetic Nephropathy by Inhibiting Pyroptosis Based on TXNIP/NLRP3 Pathway
An, X., Zhang, Y., Cao, Y., Chen, J., Qin, H., & Yang, L. (2020) · Nutrients · doi:10.3390/nu12051516 · Cited by 192 · see citing works
Hexokinase 1 cellular localization regulates the metabolic fate of glucose
Jesus, A. D., Keyhani‐Nejad, F., Pusec, C. M., Goodman, L., Geier, J., Stoolman, J. S., Stanczyk, P. J., Nguyen, T., Xu, K., Suresh, K. V., et al. (2022) · Molecular Cell · doi:10.1016/j.molcel.2022.02.028 · Cited by 183 · see citing works
Renaudin, F., Orliaguet, L., Castelli, F. A., Fenaille, F., Prignon, A., Alzaïd, F., Combes, C., Delvaux, A., Adimy, Y., Cohen-Solal, M. E., et al. (2020) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2020-217342 · Cited by 183 · see citing works
NLRP3 inflammasome activation in inflammaging
Latz, E., & Duewell, P. (2018) · Seminars in Immunology · doi:10.1016/j.smim.2018.09.001 · Cited by 174 · see citing works
Marrocco, A., & Ortiz, L. A. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.936167 · Cited by 166 · see citing works
Finucane, O. M., Sugrue, J. A., Rubio‐Araiz, A., Guillot‐Sestier, M., & Lynch, M. A. (2019) · Scientific Reports · doi:10.1038/s41598-019-40619-1 · Cited by 155 · see citing works
Luo, X., Bao, X., Weng, X., Bai, X., Yi, F., Huang, J., Liu, S., Jia, H., & Yu, B. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.120064 · Cited by 151 · see citing works
Zhang, M., Zheng, Y., Sun, Y., Li, S., Chen, L., Jin, X., Hou, X., Liu, X., Chen, Q., Li, J., et al. (2019) · Theranostics · doi:10.7150/thno.33178 · Cited by 136 · see citing works
Han, Y., Sun, W., Ren, D., Zhang, J., He, Z., Fedorova, J., Sun, X., Han, F., & Li, J. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101538 · Cited by 133 · see citing works
Tan, Y.-F., Wang, M., Chen, Z., Wang, L., & Liu, X. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2431-2 · Cited by 132 · see citing works
Cui, D., Liu, S., Tang, M., Lu, Y., Zhao, M., Mao, R., Wang, C., Yuan, Y., Li, L., Chen, Y., et al. (2019) · Phytomedicine · doi:10.1016/j.phymed.2019.153111 · Cited by 129 · see citing works
Lee, H., Fessler, M. B., Qu, P., Heymann, J. A. W., & Kopp, J. B. (2020) · BMC Nephrology · doi:10.1186/s12882-020-01921-7 · Cited by 124 · see citing works
Ahechu, P., Zozaya, G., Martí, P., Hernández-Lizoáin, J. L., Baixauli, J., Unamuno, X., Frühbeck, G., & Catalán, V. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02918 · Cited by 129 · see citing works
Targeting Innate Immunity in Cancer Therapy
Rameshbabu, S., Labadie, B. W., Argulian, A., & Patnaik, A. (2021) · Vaccines · doi:10.3390/vaccines9020138 · Cited by 118 · see citing works
Targeting NLRP3 Inflammasome Activation in Severe Asthma
Theofani, E., Semitekolou, M., Morianos, I., Samitas, Κ., & Xanthou, G. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8101615 · Cited by 118 · see citing works
Rubio‐Araiz, A., Finucane, O. M., Keogh, S., & Lynch, M. A. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1281-7 · Cited by 114 · see citing works
Kostopoulou, M., Nikolopoulos, D., Parodis, I., & Bertsias, G. K. (2019) · Current Vascular Pharmacology · doi:10.2174/1570161118666191227101636 · Cited by 114 · see citing works
Role of NLRP3 Inflammasome Activation in Obesity-Mediated Metabolic Disorders
Wani, K., AlHarthi, H., Alghamdi, A. A., Sabico, S., & Al‐Daghri, N. M. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18020511 · Cited by 114 · see citing works
Inflammasomes and Atherosclerosis: a Mixed Picture
Tall, A. R., & Bornfeldt, K. (2023) · Circulation Research · doi:10.1161/circresaha.123.321637 · Cited by 110 · see citing works
Rong, S., Wan, D., Fan, Y., Liu, S., Sun, K., Huo, J., Zhang, P., Li, X., Xie, X., Wang, F., et al. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00856 · Cited by 106 · see citing works
Pandey, A., Li, Z., Gautam, M., Ghosh, A., & Man, S. M. (2024) · Immunological Reviews · doi:10.1111/imr.13406 · Cited by 113 · see citing works
Origins and diversity of macrophages in health and disease
Sreejit, G., Fleetwood, A. J., Murphy, A. J., & Nagareddy, P. R. (2020) · Clinical & Translational Immunology · doi:10.1002/cti2.1222 · Cited by 102 · see citing works
Increasing complexity of NLRP3 inflammasome regulation
Moretti, J., & Blander, J. M. (2020) · Journal of Leukocyte Biology · doi:10.1002/jlb.3mr0520-104rr · Cited by 101 · see citing works
The NLRP3 inflammasome - interleukin 1 pathway as a therapeutic target in gout
Szekanecz, Z., Szamosi, S., Kovács, G. E., Kocsis, E., & Benkő, S. (2019) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2019.01.031 · Cited by 101 · see citing works
The Role of HDAC6 in Autophagy and NLRP3 Inflammasome
Chang, P., Li, H., Hu, H., Li, Y., & Wang, T. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.763831 · Cited by 101 · see citing works
Yu, Q., Shi, H., Ding, Z., Wang, Z., Yao, H., & Lin, R. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-022-00954-9 · Cited by 101 · see citing works
Role of NLRP3 Inflammasome in Rheumatoid Arthritis
Yin, H., Liu, N., Sigdel, K. R., & Duan, L. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.931690 · Cited by 98 · see citing works
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 95 · see citing works
Hu, Y., Shi, Y., Chen, H., Tao, M., Zhou, X., Li, J., Ma, X., Wang, Y., & Liu, N. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.858494 · Cited by 92 · see citing works
The role of uric acid in inflammasome-mediated kidney injury
Braga, T. T., Foresto‐Neto, O., & Câmara, N. O. S. (2020) · Current Opinion in Nephrology & Hypertension · doi:10.1097/mnh.0000000000000619 · Cited by 91 · see citing works
HK2: a potential regulator of osteoarthritis via glycolytic and non-glycolytic pathways
Bao, C., Zhu, S., Song, K., & He, C. (2022) · Cell Communication and Signaling · doi:10.1186/s12964-022-00943-y · Cited by 91 · see citing works
Can the emerging field of immunometabolism provide insights into neuroinflammation?
Lynch, M. A. (2019) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2019.101719 · Cited by 87 · see citing works
Inflammation and Cardiovascular Disease: The Future
Arnold, N., Lechner, K., Waldeyer, C., Shapiro, M. D., & Köenig, W. (2021) · European Cardiology Review · doi:10.15420/ecr.2020.50 · Cited by 89 · see citing works
P2Y14 receptor has a critical role in acute gouty arthritis by regulating pyroptosis of macrophages
Li, H., Jiang, W., Ye, S., Zhou, M., Liu, C., Yang, X., Hao, K., & Hu, Q. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2609-7 · Cited by 87 · see citing works
Pnpt1 mediates NLRP3 inflammasome activation by MAVS and metabolic reprogramming in macrophages
Hsu, C. G., Li, W., Sowden, M. P., Chávez, C. L., & Berk, B. C. (2023) · Cellular and Molecular Immunology · doi:10.1038/s41423-022-00962-2 · Cited by 83 · see citing works
Dinarello, C. A. (2017) · Immunological Reviews · doi:10.1111/imr.12624 · Cited by 82 · see citing works
NLRP3 inflammasome and IL-1β pathway in type 2 diabetes and atherosclerosis: Friend or foe?
Chen, X., Zhang, D., Li, Y., Wang, W., Bei, W., & Guo, J. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105885 · Cited by 84 · see citing works
Nuclear Receptors in the Control of the NLRP3 Inflammasome Pathway
Duez, H., & Pourcet, B. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.630536 · Cited by 80 · see citing works
From Mitochondria to Atherosclerosis: The Inflammation Path
Suarez-Rivero, J. M., Pastor‐Maldonado, C. J., Povea-Cabello, S., Álvarez-Córdoba, M., Villalón-García, I., Talaverón-Rey, M., Suárez-Carrillo, A., Munuera-Cabeza, M., & Sánchez-Alcázar, J. A. (2021) · Biomedicines · doi:10.3390/biomedicines9030258 · Cited by 77 · see citing works
Tassone, E. J., Cimellaro, A., Perticone, M., Hribal, M. L., Sciacqua, A., Andreozzi, F., Sesti, G., & Perticone, F. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00098 · Cited by 75 · see citing works
Chang, Y., Yuan, L., Liu, J., Muhammad, I., Cao, C., Shi, C., Zhang, Y., Li, R., Li, C., & Liu, F. (2020) · Veterinary Research · doi:10.1186/s13567-020-00796-8 · Cited by 74 · see citing works
Zhang, Y., Liu, W., Zhong, Y., Li, Q., Wu, M., Yang, L., Liu, X., & Zou, L. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/1806344 · Cited by 73 · see citing works
Effect of low-carbohydrate diets on cardiometabolic risk, insulin resistance, and metabolic syndrome
O’Neill, B. J. (2020) · Current Opinion in Endocrinology Diabetes and Obesity · doi:10.1097/med.0000000000000569 · Cited by 71 · see citing works
How Mitochondrial Metabolism Contributes to Macrophage Phenotype and Functions
Benmoussa, K., Garaude, J., & Acín‐Pérez, R. (2018) · Journal of Molecular Biology · doi:10.1016/j.jmb.2018.07.003 · Cited by 67 · see citing works
Frame, J. M., Kubaczka, C., Long, T. L., Esain, V., Soto, R. A., Hachimi, M., Jing, R., Shwartz, A., Goessling, W., Daley, G. Q., et al. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.07.015 · Cited by 67 · see citing works
The Role of NLRP3 Inflammasome Activities in Bone Diseases and Vascular Calcification
Yu, C., Zhang, C., Kuang, Z., & Zheng, Q. (2020) · Inflammation · doi:10.1007/s10753-020-01357-z · Cited by 67 · see citing works
Liu, X., Wang, Y., Wu, D., Li, S., Wang, C., Han, Z., Wang, J., Wang, K., Yang, Z., & Wei, Z. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01459 · Cited by 67 · see citing works
Qiao, S., Lv, C., Tao, Y., Miao, Y., Zhu, Y., Zhang, W., Sun, D., Yun, X., Xia, Y., Wei, Z., et al. (2020) · Cancer Letters · doi:10.1016/j.canlet.2020.08.033 · Cited by 66 · see citing works
Liu, J., Li, Y., Chen, S., Lin, Y., Lai, H., Chen, B., & Chen, T. (2020) · Frontiers in Chemistry · doi:10.3389/fchem.2020.00838 · Cited by 68 · see citing works
Regulation of the NLRP3 Inflammasome by Posttranslational Modifications
Zangiabadi, S., & Sater, A. A. A. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2100734 · Cited by 64 · see citing works
Jin, X., Dong, X., Sun, Y., Liu, Z., Liu, L., & Gu, H. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/3711371 · Cited by 61 · see citing works
Zhu, J., Chen, H., Le, Y., Guo, J., Liu, Z., Dou, X., & Lu, D. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1009229 · Cited by 61 · see citing works
Overcoming Cancer Resistance to Platinum Drugs by Inhibiting Cholesterol Metabolism
Wang, Y., Cai, L., Li, H., Chen, H., Yang, T., Tan, Y., Guo, Z., & Wang, X. (2023) · Angewandte Chemie International Edition · doi:10.1002/anie.202309043 · Cited by 61 · see citing works
Koselny, K., Mutlu, N., Minard, A. Y., Kumar, A., Krysan, D. J., & Wellington, M. A. (2018) · mBio · doi:10.1128/mbio.01204-18 · Cited by 60 · see citing works
Liu, D., Xiao, Y., Zhou, B., Gao, S., Li, L., Zhao, L., Chen, W., Dai, B., Li, Q., Duan, H., et al. (2020) · Rheumatology · doi:10.1093/rheumatology/keaa473 · Cited by 59 · see citing works
Fu, Q., Zhai, Z., Wang, Y., Xu, L., Jia, P., Xia, P., Liu, C., Zhang, X., Qin, T., & Zhang, H. (2018) · BioMed Research International · doi:10.1155/2018/1294951 · Cited by 59 · see citing works
Jiang, M., Wu, Y., Qi, L., Li, L., Song, D., Gan, J., Li, Y., Ling, X., & Song, C. (2021) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2021.109704 · Cited by 58 · see citing works
Le, S., Zhang, H., Huang, X., Chen, S., Wu, J. P., Chen, S., Ding, X., Chen, S., Zhao, J., Xu, H., et al. (2020) · Journal of Cardiovascular Pharmacology and Therapeutics · doi:10.1177/1074248420919966 · Cited by 57 · see citing works
Qi, X., Hou, R., Xie, L., Niu, M., Pan, X., & Zhu, X. (2023) · Clinical and Translational Medicine · doi:10.1002/ctm2.1257 · Cited by 55 · see citing works
Microglial Immunometabolism in Alzheimer’s Disease
Shippy, D. C., & Ulland, T. K. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.563446 · Cited by 55 · see citing works
Cosker, K., Mallach, A., Limaye, J., Piers, T. M., Staddon, J. M., Neame, S. J., Hardy, J., & Pocock, J. M. (2021) · Scientific Reports · doi:10.1038/s41598-021-91207-1 · Cited by 52 · see citing works
Zhong, Z., & Lemasters, J. J. (2018) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.13877 · Cited by 55 · see citing works
Devi, T. S., Yumnamcha, T., Yao, F., Somayajulu, M., Kowluru, R. A., & Singh, L. P. (2019) · Biology Open · doi:10.1242/bio.038521 · Cited by 56 · see citing works
Yu, Q., Guo, M., Zeng, W., Zeng, M., Zhang, X., Zhang, Y., Zhang, W., Jiang, X., & Yu, B. (2021) · Immunity Inflammation and Disease · doi:10.1002/iid3.581 · Cited by 52 · see citing works
Chen, A., Chen, Z., Zhou, Y., Wu, Y., Xia, Y., Lu, D., Fan, M., Su, L., Chen, J., Sun, A., et al. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03389-1 · Cited by 52 · see citing works
JQ1 as a BRD4 Inhibitor Blocks Inflammatory Pyroptosis-Related Acute Colon Injury Induced by LPS
Chen, L., Zhong, X., Cao, W., Mao, M., Li, W., Yang, H., Li, M., Shi, M., Zhang, Y., Deng, Y., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.609319 · Cited by 51 · see citing works
Wang, X., Li, X.-L., & Qin, L.-J. (2021) · Laboratory Investigation · doi:10.1038/s41374-021-00607-4 · Cited by 51 · see citing works
Crosstalk Between Staphylococcus aureus and Innate Immunity: Focus on Immunometabolism
Horn, C. M., & Kielian, T. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.621750 · Cited by 51 · see citing works
Zhang, T., Ding, S., & Wang, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910866 · Cited by 51 · see citing works
Comorbidities and clinical complications associated with SARS-CoV-2 infection: an overview
Gupta, A., Marzook, H., & Ahmad, F. (2022) · Clinical and Experimental Medicine · doi:10.1007/s10238-022-00821-4 · Cited by 49 · see citing works
Zhang, Z., Li, M., Li, X., Feng, Z., Luo, G., Wang, Y., & Gao, X. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03254-w · Cited by 53 · see citing works
Zhang, Z., Xie, S., Qian, J., Gao, F.-Q., Jin, W.-J., Wang, L.-Q., Yan, L., Chen, H., Yao, W., Li, M.-Q., et al. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04313-1 · Cited by 44 · see citing works
Chen, X., Li, Y., Li, J., Liu, T., Jiang, Q., Hong, Y., Wang, Q., Li, C., Guo, D., & Wang, Y. (2021) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2021.114841 · Cited by 46 · see citing works
Liu, J., Wang, C., Li, J., Yu, Y., Liu, Y., Liu, H., Peng, Q., & Guan, X. (2021) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-021-00811-2 · Cited by 46 · see citing works
Vitamin C alleviates hyperuricemia nephropathy by reducing inflammation and fibrosis
Li, H., Liu, X., Lee, M., & Li, H. (2021) · Journal of Food Science · doi:10.1111/1750-3841.15803 · Cited by 44 · see citing works
Danielski, L. G., Giustina, A. D., Bonfante, S., Goldim, M. P. D. S., Joaquim, L. D. S., Metzker, K. L. L., Biehl, E., Vieira, T. C., de Medeiros, F. D., da Rosa, N., et al. (2020) · Molecular Neurobiology · doi:10.1007/s12035-020-02089-9 · Cited by 43 · see citing works
Zhang, D., He, Y., Ye, X., Cai, Y., Xu, J., Zhang, L., Li, M., Liu, H., Wang, S., & Xia, Z. (2020) · Journal of Diabetes Investigation · doi:10.1111/jdi.13235 · Cited by 41 · see citing works
NLRP3 inflammasome inhibitor cucurbitacin B suppresses gout arthritis in mice
Xue, Y., Li, R., Fang, P., Ye, Z.-Q., Zhao, Y. L., Zhou, Y., Zhang, K., & Li, L. (2021) · Journal of Molecular Endocrinology · doi:10.1530/jme-20-0305 · Cited by 41 · see citing works
Role of Stat3 in NLRP3/caspase‐1‐mediated hippocampal neuronal pyroptosis in epileptic mice
Jiang, Q., Tang, G. Q., Zhong, X., Ding, D., Wang, H., & Li, J. (2021) · Synapse · doi:10.1002/syn.22221 · Cited by 41 · see citing works
Steroid hormone catabolites activate the pyrin inflammasome through a non-canonical mechanism
Magnotti, F., Chirita, D., Dalmon, S., Martin, A., Bronnec, P., Sousa, J., Helynck, O., Lee, W., Kastner, D. L., Chae, J. J., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111472 · Cited by 40 · see citing works
Meng, J., Li, N., Liu, X., Qiao, S., Zhou, Q., Tan, J., Zhang, T., Dong, Z., Qi, X., Kijlstra, A., et al. (2022) · Arthritis & Rheumatology · doi:10.1002/art.42420 · Cited by 40 · see citing works
Reactive oxygen species trigger inflammasome activation after intracellular microbial interaction
Rosa, C. P., Belo, T. C. A., Santos, N. C. D. M., Silva, E. N., Gasparotto, J., Corsetti, P. P., & de Almeida, L. A. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122076 · Cited by 40 · see citing works
Yang, H., Lin, P.-Y., Vadivalagan, C., Lin, Y., Lin, K., & Hseu, Y. (2023) · Archives of Toxicology · doi:10.1007/s00204-023-03456-w · Cited by 39 · see citing works
Regulation of NLRPs by reactive oxygen species: A story of crosstalk
Ziehr, B. K., & MacDonald, J. A. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2024.119823 · Cited by 39 · see citing works
- Authors
- Hughes, M. M., & O'Neill, L. A. J.
- Affiliations
- Trinity College Dublin (IE)
- Corresponding author
- Hughes, Mark M.
- Venue
- Immunological Reviews
- Publisher
- Wiley
- Published
- 2017-12-16
- Volume
- 281
- Issue
- 1
- Pages
- 88-98
- ISSN
- 0105-2896 (ISSN-L)
- 1600-065X
- OpenAlex
- W2778840601
- Cited by
- 311
- References
- 86
- Citations by year
- 2026: 12 · 2025: 24 · 2024: 50 · 2023: 48 · 2022: 49 · 2021: 49 · 2020: 47 · 2019: 18 · 2018: 13 · 2017: 1
- FWCI
- 2.02
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Immunological Reviews (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Science Foundation Ireland
- 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 › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Keywords
- NLRP3 inflammasome, macrophage metabolic reprogramming, caspase-1 activation, IL-1β, IL-18, pyroptosis, palmitate, uric acid, cholesterol crystals, ketone bodies, mitochondrial reactive oxygen species, hexokinase, glycolysis, inflammation, inflammasome inhibition
- MeSH terms
- Pyroptosis, NLR Family, Pyrin Domain-Containing 3 Protein, Animals, Cholesterol, Hexokinase, Humans, Ketone Bodies, Macrophages, Uric Acid, Reactive Oxygen Species, Palmitic Acid, Caspase 1, Inflammasomes, Cellular Reprogramming
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