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Inflammasome-mediated pyroptotic and apoptotic cell death, and defense against infection
Open accessAbstract
Cell death is an effective strategy to limit intracellular infections. Canonical inflammasomes, including NLRP3, NLRC4, and AIM2, recruit and activate caspase-1 in response to a range of microbial stimuli and endogenous danger signals. Caspase-1 then promotes the secretion of IL-1β and IL-18 and a rapid form of lytic programmed cell death termed pyroptosis. A second inflammatory caspase, mouse caspase-11, mediates pyroptotic death through an unknown non-canonical inflammasome system in response to cytosolic bacteria. In addition, recent work shows that inflammasomes can also recruit procaspase-8, initiating apoptosis. The induction of multiple pathways of cell death has probably evolved to counteract microbial evasion of cell death pathways.
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“Casp11 deletion protects mice against a challenge with cytosol-invasive bacteria [612, 620]”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [612]
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“At a molecular level, pyroptosis generally relies on the activation of one or more caspases, including CASP1, CASP3, murine CASP11, and its human homologs CASP4 and CASP5, depending on the initiating stimulus [612, 613].”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [612]
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Cites
Pyroptosis: host cell death and inflammation
Bergsbaken, T., Fink, S. L., & Cookson, B. T. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2070 · Cited by 3,288
AIM2 recognizes cytosolic dsDNA and forms a caspase-1-activating inflammasome with ASC
Hornung, V., Ablasser, A., Charrel-Dennis, M., Bauernfeind, F., Horvath, G., Caffrey, D. R., Latz, E., & Fitzgerald, K. A. (2009) · Nature · doi:10.1038/nature07725 · Cited by 2,627
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
AIM2 activates the inflammasome and cell death in response to cytoplasmic DNA
Fernandes-Alnemri, T., Yu, J.-W., Datta, P., Wu, J., & Alnemri, E. S. (2009) · Nature · doi:10.1038/nature07710 · Cited by 1,831
Caspase-1-induced pyroptosis is an innate immune effector mechanism against intracellular bacteria
Miao, E. A., Leaf, I. A., Treuting, P. M., Mao, D. P., Dors, M., Sarkar, A., Warren, S. E., Wewers, M. D., & Aderem, A. (2010) · Nature Immunology · doi:10.1038/ni.1960 · Cited by 1,336
Self-citationThe 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 1,310
Caspase‐1‐induced pyroptotic cell death
Miao, E. A., Rajan, J. V., & Aderem, A. A. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01044.x · Cited by 1,162
Self-citationCytoplasmic flagellin activates caspase-1 and secretion of interleukin 1β via Ipaf
Miao, E. A., Alpuche-Aranda, C. M., Dors, M., Clark, A. E., Bader, M. W., Miller, S. I., & Aderem, A. (2006) · Nature Immunology · doi:10.1038/ni1344 · Cited by 1,127
Self-citationBürckstümmer, T., Baumann, C., Blüml, S., Dixit, E., Dürnberger, G., Jahn, H., Planyavsky, M., Bilban, M., Colinge, J., Bennett, K. L., et al. (2009) · Nature Immunology · doi:10.1038/ni.1702 · Cited by 1,091
Innate immune recognition of bacterial ligands by NAIPs determines inflammasome specificity
Kofoed, E. M., & Vance, R. E. (2011) · Nature · doi:10.1038/nature10394 · Cited by 894
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Yu, P., Zhang, X., Liu, N., Tang, L., Peng, C., & Chen, X. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00507-5 · Cited by 2,353
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D'Arcy, M. (2019) · Cell Biology International · doi:10.1002/cbin.11137 · Cited by 2,430
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Fang, Y., Tian, S., Pan, Y., Li, W., Wang, Q., Tang, Y. R., Yu, T., Wu, X., Shi, Y., Ma, P., et al. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.109595 · Cited by 1,073
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Jørgensen, I., Rayamajhi, M., & Miao, E. A. (2017) · Nature reviews. Immunology · doi:10.1038/nri.2016.147 · Cited by 1,057
Self-citationGuidelines for the use of flow cytometry and cell sorting in immunological studies (second edition)
Cossarizza, A., Chang, H., Radbruch, A., Acs, A., Adam, D., Adam‐Klages, S., Agace, W. W., Aghaeepour, N., Akdiş, M., Allez, M., et al. (2019) · European Journal of Immunology · doi:10.1002/eji.201970107 · Cited by 1,007
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Rao, Z., Zhu, Y., Yang, P., Chen, Z., Xia, Y., Qiao, C., Liu, W., Deng, H., Li, J., Ning, P., et al. (2022) · Theranostics · doi:10.7150/thno.71086 · Cited by 835
Burdette, B. E., Esparza, A. N., Zhu, H., & Wang, S. (2021) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.02.006 · Cited by 721
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Jiang, W., Hu, J.-W., He, X.-R., Jin, W.-L., & He, X.-Y. (2021) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-021-02041-2 · Cited by 417
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Ketelut-Carneiro, N., & Fitzgerald, K. A. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.167378 · Cited by 427
Recent Insights into the Molecular Mechanisms Underlying Pyroptosis and Gasdermin Family Functions
Aglietti, R. A., & Dueber, E. C. (2017) · Trends in Immunology · doi:10.1016/j.it.2017.01.003 · Cited by 419
Qiu, Z., Lei, S., Zhao, B., Wu, Y., Su, W., Liu, M., Meng, Q., Zhou, B., Leng, Y., & Xia, Z. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/9743280 · Cited by 351
Diversity 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
Pyroptosis and its relationship to atherosclerosis
Xu, Y., Zheng, L., Hu, Y., & Wang, Q. (2017) · Clinica Chimica Acta · doi:10.1016/j.cca.2017.11.005 · Cited by 326
Cell Death in Liver Diseases: A Review
Shojaie, L., Iorga, A., & Dara, L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249682 · Cited by 309
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Fusco, R., Siracusa, R., Genovese, T., Cuzzocrea, S., & Paola, R. D. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124223 · Cited by 301
K+ Efflux Agonists Induce NLRP3 Inflammasome Activation Independently of Ca2+ Signaling
Katsnelson, M. J., Rucker, L. G., Russo, H. M., & Dubyak, G. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402658 · Cited by 278
Mechanism and regulation of pyroptosis-mediated in cancer cell death
Ruan, J., Wang, S., & Wang, J. (2020) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2020.109052 · Cited by 276
Role of pyroptosis in cardiovascular diseases
Jia, C., Chen, H. A., Zhang, J., Zhou, K., Zhuge, Y., Niu, C., Qiu, J., Rong, X., Shi, Z., Xiao, J., et al. (2018) · International Immunopharmacology · doi:10.1016/j.intimp.2018.12.028 · Cited by 268
Mechanism of membrane pore formation by human gasdermin‐D
Mulvihill, E., Sborgi, L., Mari, S. A., Pfreundschuh, M., Hiller, S., & Müller, D. J. (2018) · The EMBO Journal · doi:10.15252/embj.201798321 · Cited by 286
Lu, F., Lan, Z., Xin, Z., He, C., Guo, Z., Xia, X., & Hu, T. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.29268 · Cited by 248
Inflammasome-Mediated Inflammation in Liver Ischemia-Reperfusion Injury
Jiménez‐Castro, M. B., Cornide‐Petronio, M. E., Gracia‐Sancho, J., & Peralta, C. (2019) · Cells · doi:10.3390/cells8101131 · Cited by 244
Role of pyroptosis in spinal cord injury and its therapeutic implications
Mamun, A. A., Wu, Y., Monalisa, I., Jia, C., Zhou, K., Munir, F., & Xiao, J. (2020) · Journal of Advanced Research · doi:10.1016/j.jare.2020.08.004 · Cited by 232
Ischemia-reperfusion induces renal tubule pyroptosis via the CHOP-caspase-11 pathway
Yang, J., Yao, F.-H., Zhang, J., Ji, Z.-Y., Li, K., Zhan, J., Tong, Y., Lin, L.-R., & He, Y. (2013) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00117.2013 · Cited by 226
Pellegrini, C., Antonioli, L., López‐Castejón, G., Blandizzi, C., & Fornai, M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00036 · Cited by 220
Fleetwood, A. J., Lee, M. K. S., Singleton, W., Achuthan, A. A., Lee, M.-C., O’brien-simpson, N. M., Cook, A. D., Murphy, A. J., Dashper, S. G., Reynolds, E. C., et al. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00351 · Cited by 212
Wu, C., Chen, H. A., Zhuang, R., Zhang, H., Wang, Y., Hu, X., Xu, Y. M., Li, J., Li, Y., Wang, X., et al. (2021) · International Journal of Biological Sciences · doi:10.7150/ijbs.57825 · Cited by 206
Liu, Y.-G., Chen, J., Zhang, Z.-T., Ma, X., Chen, Y., Du, X.-M., Liu, H., Zong, Y., & Lu, G. (2017) · Cell Death and Disease · doi:10.1038/cddis.2016.460 · Cited by 190
Maltez, V. I., Tubbs, A. L., Cook, K. D., Aachoui, Y., Falcone, E. L., Holland, S. M., Whitmire, J. K., & Miao, E. A. (2015) · Immunity · doi:10.1016/j.immuni.2015.10.010 · Cited by 165
Self-citationCell death regulation: A new way for natural products to treat osteoporosis
Li, Z., Li, D., Chen, R., Gao, S., Xu, Z., & Li, N. (2022) · Pharmacological Research · doi:10.1016/j.phrs.2022.106635 · Cited by 183
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Mostowy, S., & Shenoy, A. R. (2015) · Nature reviews. Immunology · doi:10.1038/nri3877 · Cited by 190
Pellegrini, C., Antonioli, L., Calderone, V., Colucci, R., Fornai, M., & Blandizzi, C. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101806 · Cited by 174
Salinaro, A. T., Pennisi, M., Paola, R. D., Scuto, M. C., Crupi, R., Cambria, M. T., Ontario, M. L., Tomasello, M., Uva, M. G., Maiolino, L., et al. (2018) · Immunity & Ageing · doi:10.1186/s12979-017-0108-1 · Cited by 170
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Lin, L., Zhang, M.-X., Zhang, L., Zhang, D., Li, C., & Li, Y. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.809955 · Cited by 166
Kell, D. B., & Pretorius, E. (2015) · Integrative Biology · doi:10.1039/c5ib00158g · Cited by 170
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Bernaus, A., Blanco, S., & Sevilla, A. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00209 · Cited by 157
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Fann, D. Y., Santro, T., Manzanero, S., Widiapradja, A., Cheng, Y., Lee, S.-Y., Chunduri, P., Jo, D., Stranahan, A. M., Mattson, M. P., et al. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.04.017 · Cited by 148
Jørgensen, I., Lopez, J. P., Laufer, S., & Miao, E. A. (2016) · European Journal of Immunology · doi:10.1002/eji.201646647 · Cited by 148
Self-citationWei, Q., Guo, P., Mu, K., Zhang, Y., Zhao, W., Huai, W., Qiu, Y., Li, T., Ma, X., Liu, Y., et al. (2015) · Laboratory Investigation · doi:10.1038/labinvest.2015.63 · Cited by 146
Flagellin as a vaccine adjuvant
Cui, B., Liu, X., Fang, Y., Zhou, P., Zhang, Y., & Wang, Y. (2018) · Expert Review of Vaccines · doi:10.1080/14760584.2018.1457443 · Cited by 150
Pateras, I. S., Havaki, S., Nikitopoulou, X., Vougas, K. N., Townsend, P. A., Panayiotidis, M. I., Georgakilas, A. G., & Gorgoulis, V. G. (2015) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2015.06.011 · Cited by 147
Gabarin, R., Li, M., Zimmel, P. A., Marshall, J. C., Li, Y., & Zhang, H. (2021) · Journal of Innate Immunity · doi:10.1159/000515740 · Cited by 141
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Lei, A., Murphy, A. G., & Maloy, K. J. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01168 · Cited by 141
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Awad, F., Assrawi, E., Louvrier, C., Jumeau, C., Georgin‐Lavialle, S., Grateau, G., Amselem, S., Giurgea, I., & Karabina, S. (2018) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2018.02.011 · Cited by 138
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Sena-dos-Santos, C., Braga-da-Silva, C., Marques, D., Pinheiro, J. A. D. S., Ribeiro‐dos‐Santos, Â., & Cavalcante, G. C. (2021) · Cells · doi:10.3390/cells10020479 · Cited by 132
Aachoui, Y., Kajiwara, Y., Leaf, I. A., Mao, D., Ting, J. P.-Y., Coers, J., Aderem, A., Buxbaum, J. D., & Miao, E. A. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.07.016 · Cited by 125
Self-citationAziz, M., Jacob, A., & Wang, P. (2014) · Cell Death & Disease · doi:10.1038/cddis.2014.488 · Cited by 125
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Blander, J. M. (2014) · Nature reviews. Immunology · doi:10.1038/nri3720 · Cited by 127
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Qian, Z., Zhao, Y., Wan, C., Deng, Y., Zhuang, Y., Xu, Y., Zhu, Y., Lu, S., & Bao, Z. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.652963 · Cited by 127
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Self-citationYuen, B., Bayes, J. M., & Degnan, S. M. (2013) · Molecular Biology and Evolution · doi:10.1093/molbev/mst174 · Cited by 117
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Cypryk, W., Nyman, T. A., & Matikainen, S. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02188 · Cited by 121
Fang, Y., Gao, S., Wang, X., Cao, Y., Lü, J., Chen, S., Lenahan, C., Zhang, J. H., Shao, A., & Zhang, J. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00068 · Cited by 114
Ekchariyawat, P., Hamel, R., Bernard, É., Wichit, S., Surasombatpattana, P., Talignani, L., Frédéric Thomas, A., Choumet, V., Yssel, H., Desprès, P., et al. (2015) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2015.03.025 · Cited by 106
Askarian, F., Wagner, T. M., Johannessen, M., & Nizet, V. (2018) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuy025 · Cited by 109
Pellegrini, C., Fornai, M., Antonioli, L., Blandizzi, C., & Calderone, V. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20122876 · Cited by 113
Zhou, R., Yang, X., Li, X., Qu, Y., Huang, Q., Sun, X., & Mu, D. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1651-9 · Cited by 100
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Varela, M., Figueras, A. J., & Novoa, B. (2016) · Antiviral Research · doi:10.1016/j.antiviral.2016.12.013 · Cited by 99
Yang, S., Li, Y., Zhou, L., Wang, X., Liu, L., & Wu, M. (2024) · Cell Death Discovery · doi:10.1038/s41420-023-01796-1 · Cited by 98
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Self-citationInteraction of Mycobacterium tuberculosis with Host Cell Death PathwaysPreprint
Srinivasan, L., Ahlbrand, S. E., & Briken, V. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a022459 · Cited by 90
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Iorga, A., & Dara, L. (2019) · Advances in pharmacology · doi:10.1016/bs.apha.2019.01.006 · Cited by 89
Zhang, Y., Fang, C., Zhang, W., & Zhang, K. (2022) · Matter · doi:10.1016/j.matt.2022.08.026 · Cited by 88
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Xia, X., Wang, X., Zheng, Y., Jiang, J., & Hu, J. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27909 · Cited by 86
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Mamun, A. A., Wu, Y., Nasrin, F., Akter, A., Taniya, M. A., Munir, F., Jia, C., & Xiao, J. (2021) · Journal of Inflammation Research · doi:10.2147/jir.s291453 · Cited by 83
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Kovacs, S. B., Oh, C., Maltez, V. I., McGlaughon, B. D., Verma, A., Miao, E. A., & Aachoui, Y. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107967 · Cited by 78
Self-citationSchaale, K., Peters, K. M., Murthy, A. M. V., Fritzsche, A. K., Phan, M., Totsika, M., Robertson, A. A. B., Nichols, K. B., Cooper, M. A., Stacey, K. J., et al. (2015) · Mucosal Immunology · doi:10.1038/mi.2015.44 · Cited by 78
Self-citationPyroptosis in diabetes and diabetic nephropathy
Zhaohui, C., Huang, D., Tang, C., Lu, Y., Huang, S., Peng, C., & Hu, X. (2022) · Clinica Chimica Acta · doi:10.1016/j.cca.2022.04.011 · Cited by 78
Bitto, N. J., Baker, P. J., Dowling, J. K., Wray‐McCann, G., Paoli, A. D., Tran, L. S., Leung, P. L., Stacey, K. J., Mansell, A. S., Masters, S. L., et al. (2018) · Immunology and Cell Biology · doi:10.1111/imcb.12190 · Cited by 80
Self-citationLi, Z., Xu, H., Liu, X., Hong, Y., Lou, H., Liu, H., Bai, X., Wang, L., Li, X., Monayo, S. M., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-03120-6 · Cited by 76
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Wan, L., Yuan, X., Liu, M., & Xue, B. (2017) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2017.5667 · Cited by 75
Naji, A., Muzembo, B. A., Yagyu, K.-I., Baba, N., Deschaseaux, F., Sensebé, L., & Suganuma, N. (2016) · Scientific Reports · doi:10.1038/srep26162 · Cited by 73
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Tsai, Y., Chiang, K., Hung, J., Chang, W., Lin, H., Shieh, J., Chong, I., & Hsu, Y. (2017) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2017.3310 · Cited by 71
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Khweek, A. A., & Amer, A. O. (2020) · Immunological Reviews · doi:10.1111/imr.12910 · Cited by 71
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Wang, L., Yan, J. Y., Niu, H., Huang, R., & Wu, S. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00078 · Cited by 71
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Blader, I. J., & Koshy, A. A. (2014) · Eukaryotic Cell · doi:10.1128/ec.00081-14 · Cited by 67
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Pillon, N. J., Chan, K. L., Zhang, S., Mejdani, M., Jacobson, M. R., Ducos, A., Bilan, P. J., Niu, W., & Klip, A. (2016) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00296.2016 · Cited by 70
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Guo, H., Xie, M., Zhou, C., & Zheng, M. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.02.060 · Cited by 67
Varela, M., Romero, A., Dios, S., van der Vaart, M., Figueras, A. J., Meijer, A. H., & Novoa, B. (2014) · Journal of Virology · doi:10.1128/jvi.02056-14 · Cited by 67
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Jia, Y., Wang, X., Deng, Y., Li, S., Xu, X., Qin, Y., & Peng, L. J. (2023) · Journal of Cancer · doi:10.7150/jca.77965 · Cited by 66
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He, L., Huang, Z., Huang, K., Chen, R., Nguyen, N. T., Wang, R., Cai, X., Huang, Z., Siwko, S. K., Walker, J. R., et al. (2021) · Advanced Science · doi:10.1002/advs.202100424 · Cited by 63
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Metadata
- Authors
- Aachoui, Y., Sagulenko, V., Miao, E. A., & Stacey, K. J.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- The University of Queensland (AU)
- Corresponding author
- Miao, Edward A
- Stacey, Katryn J
- Venue
- Current Opinion in Microbiology
- Publisher
- Elsevier BV
- Published
- 2013-06
- Volume
- 16
- Issue
- 3
- Pages
- 319-326
- ISSN
- 1369-5274 (ISSN-L)
- PMC
- PMC3742712
- OpenAlex
- W2077730689
- Cited by
- 296
- References
- 58
- Citations by year
- 2026: 13 · 2025: 16 · 2024: 22 · 2023: 30 · 2022: 39 · 2021: 32 · 2020: 24 · 2019: 29 · 2018: 19 · 2017: 17 · 2016: 14 · 2015: 21 · 2014: 13 · 2013: 7
- FWCI
- 1.73
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Current Opinion in Microbiology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Australian Research Council Future Fellowship (FT0991576)
- National Health and Medical Research Council (631472, 1010887)
- National Institute of Health (AI097518, AI057141)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Keywords
- inflammasome, pyroptosis, apoptosis, caspase-1, caspase-11, NLRP3 inflammasome, NLRC4 inflammasome, AIM2 inflammasome, IL-1β, IL-18, procaspase-8, intracellular infection, host defense against infection
- MeSH terms
- Animals, Communicable Diseases, Humans, Signal Transduction, Cytokines, Cell Death, Caspases, Mice, Inflammasomes
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