The DOI matches its Crossref record; 45 of the 45 references it cites were found in a registry or an index.
Cytoplasmic flagellin activates caspase-1 and secretion of interleukin 1β via Ipaf
Abstract
Macrophages respond to Salmonella typhimurium infection via Ipaf, a NACHT-leucine-rich repeat family member that activates caspase-1 and secretion of interleukin 1beta. However, the specific microbial salmonella-derived agonist responsible for activating Ipaf is unknown. We show here that cytosolic bacterial flagellin activated caspase-1 through Ipaf but was independent of Toll-like receptor 5, a known flagellin sensor. Stimulation of the Ipaf pathway in macrophages after infection required a functional salmonella pathogenicity island 1 type III secretion system but not the flagellar type III secretion system; furthermore, Ipaf activation could be recapitulated by the introduction of purified flagellin directly into the cytoplasm. These observations raise the possibility that the salmonella pathogenicity island 1 type III secretion system cannot completely exclude 'promiscuous' secretion of flagellin and that the host capitalizes on this 'error' by activating a potent host-defense pathway.
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
“By contrast, IL-1β production was independent of the Ipaf inflammasome, which has been shown to activate caspase-1 and produce IL-1β in response to flagellin from Salmonella typhimurium and Legionella pneumophila (fig.S4) (11,12).”
From Innate Immune Activation Through Nalp3 Inflammasome Sensing of Asbestos and Silica (2008) · cites this paper as [11]
Citations
Cites
Akira, S., & Takeda, K. (2004) · Nature reviews. Immunology · doi:10.1038/nri1391 · Cited by 8,312
Defective LPS Signaling in C3H/HeJ and C57BL/10ScCr Mice: Mutations in Tlr4 Gene
Poltorak, A., He, X., Smirnova, I., Liu, M.-Y., Huffel, C. V., Du, X., Birdwell, D., Alejos, E., Silva, M., Galanos, C., et al. (1998) · Science · doi:10.1126/science.282.5396.2085 · Cited by 7,631
Martinon, F., Burns, K., & Tschopp, J. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00599-3 · Cited by 6,066
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
The innate immune response to bacterial flagellin is mediated by Toll-like receptor 5
Hayashi, F., Smith, K. D., Ozinsky, A., Hawn, T. R., Yi, E. C., Goodlett, D. R., Eng, J. K., Akira, S., Underhill, D. M., & Aderem, A. A. (2001) · Nature · doi:10.1038/35074106 · Cited by 3,605
Self-citationCryopyrin 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
Nod2 Is a General Sensor of Peptidoglycan through Muramyl Dipeptide (MDP) Detection
Girardin, S. E., Boneca, I. G., Viala, J., Chamaillard, M., Labigne-Roussel, A., Thomas, G. D., Philpott, D. J., & Sansonetti, P. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.c200651200 · Cited by 2,397
Differential activation of the inflammasome by caspase-1 adaptors ASC and Ipaf
Mariathasan, S., Newton, K., Monack, D. M., Vucic, D., French, D. M., Lee, W. P., Roose-Girma, M., Erickson, S. L., & Dixit, V. M. (2004) · Nature · doi:10.1038/nature02664 · Cited by 1,864
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
Host Recognition of Bacterial Muramyl Dipeptide Mediated through NOD2
Inohara, N., Ogura, Y., Fontalba, A., Gutierrez, O., Pons, F., Crespo, J., Fukase, K., Inamura, S., Kusumoto, S., Hashimoto, M., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.c200673200 · Cited by 1,694
Flagged first, then by citations
Cited by
Sorted by citations
Items 601–700 of 1,000
Sensing bacterial infections by NAIP receptors in NLRC4 inflammasome activation
Gong, Y., & Shao, F. (2012) · Protein & Cell · doi:10.1007/s13238-012-2028-3 · Cited by 42
Hoffmann, C., Galle, M., Dilling, S., Käppeli, R., Müller, A. J., Songhet, P., Beyaert, R., & Hardt, W. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012477 · Cited by 43
Interactions between Nod-Like Receptors and Intestinal Bacteria
de Zoete, M. R., & Flavell, R. A. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00462 · Cited by 43
Topical Flagellin-Mediated Innate Defense against Candida albicans Keratitis
Gao, N., Kumar, A., Guo, H., Wu, X., Wheater, M. K., & Yu, F. X. (2011) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.10-5928 · Cited by 45
Modulation of Host Cell Processes by T3SS Effectors
Shenoy, A. R., Furniss, R. C. D., Goddard, P. J., & Clements, A. (2018) · Current topics in microbiology and immunology · doi:10.1007/82_2018_106 · Cited by 43
Infections, immunity and atherosclerosis: Pathogenic mechanisms and unsolved questions
Pedicino, D., Giglio, A. F., Galiffa, V. A., Cialdella, P., Trotta, F., Graziani, F., & Liuzzo, G. (2012) · International Journal of Cardiology · doi:10.1016/j.ijcard.2012.05.098 · Cited by 44
NLR activation takes a direct route
Monie, T. P. (2013) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2013.01.001 · Cited by 42
Kurup, S. P., & Tarleton, R. L. (2013) · Nature Communications · doi:10.1038/ncomms3616 · Cited by 42
Kienes, I., Weidl, T., Mirza, N., Chamaillard, M., & Kufer, T. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22031301 · Cited by 42
Pyroptosis: Induction and inhibition strategies for immunotherapy of diseases
Wu, J., Wang, H., Gao, P., & Ouyang, S. (2024) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2024.06.026 · Cited by 43
More than a locomotive organelle: flagella in Escherichia coli
Zhou, M., Yang, Y., Chen, P., Hu, H., Hardwidge, P. R., & Zhu, G. (2015) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-015-6946-x · Cited by 41
Caution, K., Gavrilin, M. A., Tazi, M., Kanneganti, A., Layman, D., Hoque, S., Krause, K., & Amer, A. O. (2015) · Scientific Reports · doi:10.1038/srep18479 · Cited by 45
Immunity to uropathogens: the emerging roles of inflammasomes
Hamilton, C., Tan, L., Miethke, T., & Anand, P. (2017) · Nature Reviews Urology · doi:10.1038/nrurol.2017.25 · Cited by 40
Shen, Y., Chen, L., Wang, M., Lin, D., Liang, Z. T., Song, P., Yuan, Q., Tang, H., Li, W., Duan, K., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-01619-1 · Cited by 41
Recognition of Intracellular Bacteria by Inflammasomes
Brož, P. (2019) · Microbiology Spectrum · doi:10.1128/microbiolspec.bai-0003-2019 · Cited by 41
Virulence factors perforate the pathogen-containing vacuole to signal efferocytosis
Hiyoshi, H., English, B. C., Diaz-Ochoa, V. E., Wangdi, T., Zhang, L. F., Sakaguchi, M., Haneda, T., Tsolis, R. M., & Bäumler, A. J. (2021) · Cell Host & Microbe · doi:10.1016/j.chom.2021.12.001 · Cited by 41
Jones, J. W. M., Brož, P., & Monack, D. M. (2011) · Frontiers in Microbiology · doi:10.3389/fmicb.2011.00016 · Cited by 40
Recognition of Extracellular Bacteria by NLRs and Its Role in the Development of Adaptive Immunity
Ferrand, J., & Ferrero, R. L. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00344 · Cited by 41
MyD88-Dependent Signaling Contributes to Host Defense against Ehrlichial Infection
Koh, Y., Koo, J., Biswas, A., & Kobayashi, K. S. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011758 · Cited by 40
Fortier, A. H., Doiron, K., Saleh, M., Grinstein, S., & Gros, P. (2009) · Infection and Immunity · doi:10.1128/iai.01546-08 · Cited by 42
Nalbandian, A., Khan, A. A., Srivastava, R., Llewellyn, K. J., Tan, B., Shukr, N., Fazli, Y., Kimonis, V. E., & BenMohamed, L. (2016) · Inflammation · doi:10.1007/s10753-016-0449-5 · Cited by 42
RetractedThe Role of the Host in Driving Phenotypic Heterogeneity in Salmonella
Tsai, C. N., & Coombes, B. K. (2019) · Trends in Microbiology · doi:10.1016/j.tim.2019.01.004 · Cited by 39
Yang, J., Zhang, E., Liu, F., Zhang, Y., Zhong, M., Li, Y., Zhou, D., Chen, Y.-Q., Cao, Y., Xiao, Y., et al. (2013) · Journal of Innate Immunity · doi:10.1159/000351476 · Cited by 41
Pyroptosis in health and disease
Imre, G. (2024) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00503.2023 · Cited by 39
Inflammasome Activation by Campylobacter jejuni
Bouwman, L. I., de Zoete, M. R., Bleumink‐Pluym, N. M. C., Flavell, R. A., & van Putten, J. P. M. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1400648 · Cited by 39
ZIKV infection regulates inflammasomes pathway for replication in monocytes
Khaiboullina, S. F., Uppal, T., Sarkar, R., Gorzalski, A. J., Jeor, S. S., & Verma, S. C. (2017) · Scientific Reports · doi:10.1038/s41598-017-16072-3 · Cited by 40
Adjuvant Strategies for Lactic Acid Bacterial Mucosal Vaccines
Vilander, A. C., & Dean, G. A. (2019) · Vaccines · doi:10.3390/vaccines7040150 · Cited by 40
Caspase‐7 mediates caspase‐1‐induced apoptosis independently of Bid
Mahib, M. R., Hosojima, S., Kushiyama, H., Kinoshita, T., Shiroishi, T., Suda, T., & Tsuchiya, K. (2019) · Microbiology and Immunology · doi:10.1111/1348-0421.12756 · Cited by 39
Modulation of caspases and their non-apoptotic functions byLegionella pneumophila
Amer, A. O. (2009) · Cellular Microbiology · doi:10.1111/j.1462-5822.2009.01401.x · Cited by 39
Levin, T. C., Wickliffe, K. E., Leppla, S. H., & Moayeri, M. (2008) · Cellular Microbiology · doi:10.1111/j.1462-5822.2008.01220.x · Cited by 39
Activation of NLRC4 downregulates TLR5-mediated antibody immune responses against flagellin
Li, W., Yang, J., Zhang, E., Zhong, M., Xiao, Y., Yu, J., Zhou, D., Cao, Y., Yang, Y., Li, Y., et al. (2015) · Cellular and Molecular Immunology · doi:10.1038/cmi.2015.33 · Cited by 38
Biswas, G., Bi̇len, S., Kono, T., Sakai, M., & Hikima, J.-I. (2015) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2015.10.008 · Cited by 39
Using PAMPs and DAMPs as adjuvants in cancer vaccines
Sun, H., Hu, W., Yan, Y., Zhang, Z., Chen, Y., Yao, X., Teng, L., Wang, X., Chai, D., Zheng, J., et al. (2021) · Human Vaccines & Immunotherapeutics · doi:10.1080/21645515.2021.1964316 · Cited by 40
Sundquist, M., & Wick, M. J. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.0708413 · Cited by 38
Novel insights into NOD-like receptors in renal diseases
Jin, J., Zhou, T.-J., Ren, G., Cai, L., & Meng, X. (2022) · Acta Pharmacologica Sinica · doi:10.1038/s41401-022-00886-7 · Cited by 37
Inflammasomes and their role in PANoptosomes
Nadella, V., & Kanneganti, T. (2024) · Current Opinion in Immunology · doi:10.1016/j.coi.2024.102489 · Cited by 36
CD103−CD11b+ dendritic cells regulate the sensitivity of CD4 T-cell responses to bacterial flagellin
Atif, S. M., Uematsu, S., Akira, S., & McSorley, S. J. (2013) · Mucosal Immunology · doi:10.1038/mi.2013.25 · Cited by 37
Karavolos, M. H., Bulmer, D. M., Winzer, K., Wilson, M., Mastroeni, P., Williams, P. M., & Khan, C. M. A. (2007) · Journal of Bacteriology · doi:10.1128/jb.01253-07 · Cited by 37
Salmonella and the Inflammasome: Battle for Intracellular Dominance
Crowley, S. M., Knodler, L. A., & Vallance, B. A. (2016) · Current topics in microbiology and immunology · doi:10.1007/978-3-319-41171-2_3 · Cited by 43
Lehmann, S., Esch, E., Hartmann, P., Goswami, A., Nikolin, S., Weis, J., Beyer, C., & Johann, S. (2018) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12483 · Cited by 41
Live‐cell fluorescence imaging reveals dynamic production and loss of bacterial flagella
Zhuang, X., Guo, S., Li, Z., Zhao, Z., Kojima, S., Homma, M., Wang, P., Lo, C., & Bai, F. (2020) · Molecular Microbiology · doi:10.1111/mmi.14511 · Cited by 37
Interaction between IgA and gut microbiota and its role in controlling metabolic syndrome
Guo, J., Han, X., Huang, W., You, Y., & Zhan, J. (2020) · Obesity Reviews · doi:10.1111/obr.13155 · Cited by 38
dos Reis, E. C., Leal, V. N. C., Soares, J. L. D. S., Fernandes, F. P., de Lima, D. S., de Alencar, B. C., & Pontillo, A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01291 · Cited by 37
Regulation of intestinal microbiota by the NLR protein family
Biswas, A., & Kobayashi, K. S. (2013) · International Immunology · doi:10.1093/intimm/dxs116 · Cited by 40
Vance, R. E. (2010) · Journal of Clinical Immunology · doi:10.1007/s10875-010-9389-2 · Cited by 35
Shigella Infection of Intestinal Epithelium and Circumvention of the Host Innate Defense System
Ashida, H., Ogawa, M., Mimuro, H., & Sasakawa, C. (2009) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-01846-6_8 · Cited by 37
Generation of a Listeria vaccine strain by enhanced caspase‐1 activation
Warren, S. E., Duong, H., Mao, D. P., Armstrong, A. M., Rajan, J. V., Miao, E. A., & Aderem, A. A. (2011) · European Journal of Immunology · doi:10.1002/eji.201041214 · Cited by 35
Self-citationG Protein Signaling Modulator-3 Inhibits the Inflammasome Activity of NLRP3
Giguère, P. M., Gall, B., Ezekwe, E., Laroche, G., Buckley, B. K., Kébaïer, C., Wilson, J. E., Ting, J. P. ‐., Siderovski, D. P., & Duncan, J. A. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.578393 · Cited by 35
Yim, L., Sasías, S., Martínez, A., Betancor, L., Estevez, V., Scavone, P., Bielli, A., Sirok, A., & Chabalgoity, J. A. (2014) · Infection and Immunity · doi:10.1128/iai.01336-13 · Cited by 38
Kranc, W., Brązert, M., Ożegowska, K., Nawrocki, M. J., Budna, J., Celichowski, P., Dyszkiewicz-Konwińska, M., Jankowski, M., Ješeta, M., Pawelczyk, L. A., et al. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18122673 · Cited by 33
Losa, D., Köhler, T., Bellec, J., Dudez, T. S., Crespin, S., Bacchetta, M., Boulanger, P. A., Hong, S. S., Morel, S., Nguyen, T. H., et al. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1301294 · Cited by 35
Inflammasomes and the microbiota–partners in the preservation of mucosal homeostasis
Levy, M., Thaiss, C. A., Katz, M. N., Suez, J., & Elinav, E. (2015) · Seminars in Immunopathology · doi:10.1007/s00281-014-0451-7 · Cited by 34
Tolle, L. B., Yu, F. X., Kovach, M. A., Ballinger, M. N., Newstead, M. W., Zeng, X., Núñez, G., & Standiford, T. J. (2014) · Journal of Innate Immunity · doi:10.1159/000367790 · Cited by 34
Casson, C. N., & Shin, S. (2013) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2013.00111 · Cited by 34
Blimp-1/PRDM1 Mediates Transcriptional Suppression of the NLR Gene NLRP12/Monarch-1
Lord, C. A., Savitsky, D. A., Sitcheran, R., Calame, K. L., Wright, J. R., Ting, J. P.-Y., & Williams, K. L. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0801692 · Cited by 35
Hausmann, A., Russo, G., Grossmann, J., Zünd, M., Schwank, G., Aebersold, R. H., Liu, Y., Sellin, M. E., & Hardt, W. (2020) · Cellular Microbiology · doi:10.1111/cmi.13191 · Cited by 33
Nod-like receptors in intestinal host defense
Robertson, S. J., & Girardin, S. E. (2012) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e32835a68ea · Cited by 33
Conrad, S. J., El-Aswad, M., Kurban, E., Jeng, D., Tripp, B. C., Nutting, C. W., Eversole, R. R., Mackenzie, C. D., & Essani, K. (2015) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-015-0131-z · Cited by 33
Exosomes Regulate NLRP3 Inflammasome in Diseases
Li, Z., Chen, X., Tao, J., Shi, A., Zhang, J., & Yu, P. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.802509 · Cited by 36
Regulation of Toll-like Receptor 5 Gene Expression and Function on Mucosal Dendritic Cells
Feng, T., Cong, Y., Alexander, K. L., & Elson, C. O. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035918 · Cited by 33
NOD2 Signaling Contributes to Host Defense in the Lungs against Escherichia coli Infection
Theivanthiran, B., Batra, S., Balamayooran, G., Cai, S., Kobayashi, K. S., Flavell, R. A., & Jeyaseelan, S. (2012) · Infection and Immunity · doi:10.1128/iai.06230-11 · Cited by 33
RetractedInhibition of Airway Allergic Disease by Co-Administration of Flagellin with Allergen
Lee, S. E., Koh, Y., Kim, M.-K., Kim, Y. R., Kim, S. Y., Nam, J. H., Choi, Y. D., Bae, S. J., Ko, Y. J., Ryu, H.-J., et al. (2007) · Journal of Clinical Immunology · doi:10.1007/s10875-007-9138-3 · Cited by 33
Manipulation of the host cell death pathway byShigella
Ashida, H., Kim, M., & Sasakawa, C. (2014) · Cellular Microbiology · doi:10.1111/cmi.12367 · Cited by 38
Osawa, R., Williams, K. L., & Singh, N. (2010) · Journal of Infection · doi:10.1016/j.jinf.2010.10.002 · Cited by 34
Wangdi, T., Mijares, L. A., & Kazmierczak, B. I. (2010) · Infection and Immunity · doi:10.1128/iai.00744-10 · Cited by 32
Tourlomousis, P., Wright, J. A., Bittante, A., Hopkins, L., Webster, S. J., Bryant, O. J., Mastroeni, P., Maskell, D. J., & Bryant, C. E. (2020) · Nature Microbiology · doi:10.1038/s41564-020-00801-y · Cited by 30
Biological Functions of Gasdermins in Cancer: From Molecular Mechanisms to Therapeutic Potential
Wang, M., Chen, X., & Zhang, Y. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.638710 · Cited by 33
Brewer, S. M., Twittenhoff, C., Kortmann, J., Brubaker, S. W., Honeycutt, J. D., Massis, L. M., Pham, T. H. M., Narberhaus, F., & Monack, D. M. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009345 · Cited by 35
Shigella OspC3 Suppresses Murine Cytosolic LPS Sensing
Oh, C., Verma, A., Hafeez, M., Hogland, B. A., & Aachoui, Y. (2021) · iScience · doi:10.1016/j.isci.2021.102910 · Cited by 32
Intestinal innate immunity and the pathogenesis of Salmonella enteritis
Srikanth, C. V., & Cherayil, B. J. (2007) · Immunologic Research · doi:10.1007/bf02686090 · Cited by 32
Eltom, S. M., Belvisi, M. G., Yew‐Booth, L., Dekkak, B., Maher, S. A., Dubuis, E. D., Jones, V. M., Fitzgerald, K. A., & Birrell, M. A. (2014) · Respiratory Research · doi:10.1186/s12931-014-0087-0 · Cited by 34
Kajikawa, A., & Igimi, S. (2010) · Vaccine · doi:10.1016/j.vaccine.2010.02.077 · Cited by 32
Mechanism of NAIP—NLRC4 inflammasome activation revealed by cryo-EM structure of unliganded NAIP5
Paidimuddala, B., Cao, J., Nash, G., Xie, Q., Wu, H., & Zhang, L. (2023) · Nature Structural & Molecular Biology · doi:10.1038/s41594-022-00889-2 · Cited by 31
Pandeya, A., Zhang, Y., Cui, J., Yang, L., Li, J., Zhang, G., Wu, C., Li, Z., & Wei, Y. (2023) · Microbiological Research · doi:10.1016/j.micres.2023.127460 · Cited by 34
Activation and Regulation of NLRP3 by Sterile and Infectious Insults
Banerjee, S. K., Chatterjee, A., Gupta, S., & Nagar, A. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.896353 · Cited by 31
Inflammasome Complexes: Crucial mediators in osteoimmunology and bone diseases.
Zhou, F., Zhang, G., Wu, Y.-Y., & Xiong, Y. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.109072 · Cited by 26
Bens, M., Vimont, S., Mkaddem, S. B., Chassin, C., Goujon, J., Balloy, V., Chignard, M., Werts, C., & Vandewalle, A. (2014) · Cellular Microbiology · doi:10.1111/cmi.12306 · Cited by 31
Takagi, M., Takakubo, Y., Pajarinen, J., Naganuma, Y., Oki, H., Maruyama, M., & Goodman, S. B. (2017) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2017.05.004 · Cited by 31
Regulation and Sensing of Inflammasomes and Their Impact on Intestinal Health
Ranson, N., Kunde, D., & Eri, R. D. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18112379 · Cited by 30
Beyond canonical inflammasomes: emerging pathways in IL-1-mediated autoinflammatory disease
Lukens, J. R., & Kanneganti, T. (2014) · Seminars in Immunopathology · doi:10.1007/s00281-014-0434-8 · Cited by 30
Fournier, B., Williams, I. R., Gewirtz, A. T., & Neish, A. S. (2009) · Infection and Immunity · doi:10.1128/iai.00656-09 · Cited by 30
Kufer, T. A., Nigro, G., & Sansonetti, P. J. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.mchd-0021-2015 · Cited by 30
Wang, W., Peng, Z., Baloch, Z., Hu, Y., Xu, J., Zhang, W., Fanning, S., & Li, F. (2017) · Microbiological Research · doi:10.1016/j.micres.2017.07.006 · Cited by 30
TLR5 recognizes Aeromonas hydrophila flagellin and interacts with MyD88 in Nile tilapia
Gao, F., Pang, J.-C., Lu, M., Liu, Z., Wang, M., Ke, X., Yi, M., & Cao, J. (2022) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2022.104409 · Cited by 29
The IL-23 axis in Salmonella gastroenteritis
Godinez, I., Keestra, A. M., Spees, A. M., & Bäumler, A. J. (2011) · Cellular Microbiology · doi:10.1111/j.1462-5822.2011.01637.x · Cited by 30
Badea, L., Beatson, S. A., Kaparakis‐Liaskos, M., Ferrero, R. L., & Hartland, E. L. (2009) · BMC Microbiology · doi:10.1186/1471-2180-9-30 · Cited by 30
Yoon, G. S., Dong, C., Gao, N., Kumar, A., Standiford, T. J., & Yu, F. X. (2013) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.13-12453 · Cited by 30
Adriaensen, C., Greve, H. D., Tian, J. Q., Craeye, S. D., Gubbels, E., Eeckhaut, V., Immerseel, F. V., Ducatelle, R., Kumar, M. C., & Hernálsteens, J.-P. (2007) · Infection and Immunity · doi:10.1128/iai.01357-06 · Cited by 30
Keratin 6a reorganization for ubiquitin–proteasomal processing is a direct antimicrobial response
Chan, J., Yuen, D., Too, P. H.-M., Sun, Y., Willard, B. B., Man, D., & Tam, C. K. P. (2017) · The Journal of Cell Biology · doi:10.1083/jcb.201704186 · Cited by 29
The Inflammasome: Regulation of Nitric Oxide and Antimicrobial Host Defence
Ramachandran, R. A., Lupfer, C. R., & Zaki, H. (2018) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/bs.ampbs.2018.01.004 · Cited by 32
NLRP3 Inflammasomes: Dual Function in Infectious Diseases
Li, Y., Qiang, R., Cao, Z.-M., Wu, Q., Wang, J., & Lyu, W. (2024) · The Journal of Immunology · doi:10.4049/jimmunol.2300745 · Cited by 31
Su, Z., Lan, J., Wang, Y., Ni, M., Yang, J., Liang, D., Zeng, H., & Yang, M. (2025) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2025.01.028 · Cited by 29
Regulatory Evolution Drives Evasion of Host Inflammasomes by Salmonella Typhimurium
Ilyas, B., Mulder, D. T., Little, D. J., Elhenawy, W., Banda, M. M., Pérez‐Morales, D., Tsai, C. N., Chau, N. Y. E., Bustamante, V. H., & Coombes, B. K. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.09.078 · Cited by 29
Mylona, E., Sanchez‐Garrido, J., Thu, T. N. H., Dongol, S., Karkey, A., Baker, S. G., Shenoy, A. R., & Frankel, G. M. (2020) · Cellular Microbiology · doi:10.1111/cmi.13306 · Cited by 27
Gao, N., Yoon, G. S., Liu, X., Mi, X., Chen, W., Standiford, T. J., & Yu, F.-S. (2013) · Mucosal Immunology · doi:10.1038/mi.2012.137 · Cited by 32
Role for the Chlamydial Type III Secretion Apparatus in Host Cytokine Expression
Prantner, D., & Nagarajan, U. M. (2008) · Infection and Immunity · doi:10.1128/iai.00963-08 · Cited by 29
Unveiling the pathogen behind the vacuole
Liehl, P., Zuzarte‐Luís, V., & Mota, M. M. (2015) · Nature Reviews Microbiology · doi:10.1038/nrmicro3504 · Cited by 29
Masud, S., van der Burg, L., Storm, L., Prajsnar, T. K., & Meijer, A. H. (2019) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2019.00279 · Cited by 28
Orchestration of pathogen recognition by inflammasome diversity: Variations on a common theme
Martinon, F. (2007) · European Journal of Immunology · doi:10.1002/eji.200737871 · Cited by 29
Tahoun, A. A. E., Jensen, K., Corripio‐Miyar, Y., McAteer, S. P., Corbishley, A., Mahajan, A., Brown, H. K., Frew, D., Aumeunier, A., Smith, D. G., et al. (2015) · Veterinary Research · doi:10.1186/s13567-014-0135-2 · Cited by 28
Metadata
- Authors
- Miao, E. A., Alpuche-Aranda, C. M., Dors, M., Clark, A. E., Bader, M. W., Miller, S. I., & Aderem, A.
- Affiliations
- University of Washington (US)
- Hospital Infantil de México Federico Gómez (MX)
- Institute for Systems Biology (US)
- Corresponding author
- Aderem, Alan
- Venue
- Nature Immunology
- Published
- 2006-04-30
- Volume
- 7
- Issue
- 6
- Pages
- 569-575
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- OpenAlex
- W1987463569
- Cited by
- 1,127
- References
- 45
- Citations by year
- 2026: 15 · 2025: 21 · 2024: 32 · 2023: 49 · 2022: 48 · 2021: 37 · 2020: 50 · 2019: 51 · 2018: 44 · 2017: 56 · 2016: 47 · 2015: 56 · 2014: 78 · 2013: 85 · 2012: 70
- FWCI
- 33.13
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Genentech
- 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 › Agricultural and Biological Sciences › Food Science › Salmonella and Campylobacter epidemiology
- Keywords
- caspase-1 activation, interleukin-1β secretion, interstitial pneumonia with autoimmune features, Salmonella typhimurium, macrophages, pathogenicity island 1, type III secretion system, TLR5, innate immunity
- MeSH terms
- Animals, Bacterial Proteins, Calcium-Binding Proteins, Cytoplasm, Enzyme Activation, Flagellin, Interleukin-1, Macrophages, Mice, Mutant Strains, Mutation, Salmonella Infections, Salmonella typhimurium, Caspase 1, Protein Transport, Apoptosis Regulatory Proteins, Toll-Like Receptor 5, Mice
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