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Differential roles of MDA5 and RIG-I helicases in the recognition of RNA viruses
Abstract
The innate immune system senses viral infection by recognizing a variety of viral components (including double-stranded (ds)RNA) and triggers antiviral responses. The cytoplasmic helicase proteins RIG-I (retinoic-acid-inducible protein I, also known as Ddx58) and MDA5 (melanoma-differentiation-associated gene 5, also known as Ifih1 or Helicard) have been implicated in viral dsRNA recognition. In vitro studies suggest that both RIG-I and MDA5 detect RNA viruses and polyinosine-polycytidylic acid (poly(I:C)), a synthetic dsRNA analogue. Although a critical role for RIG-I in the recognition of several RNA viruses has been clarified, the functional role of MDA5 and the relationship between these dsRNA detectors in vivo are yet to be determined. Here we use mice deficient in MDA5 (MDA5-/-) to show that MDA5 and RIG-I recognize different types of dsRNAs: MDA5 recognizes poly(I:C), and RIG-I detects in vitro transcribed dsRNAs. RNA viruses are also differentially recognized by RIG-I and MDA5. We find that RIG-I is essential for the production of interferons in response to RNA viruses including paramyxoviruses, influenza virus and Japanese encephalitis virus, whereas MDA5 is critical for picornavirus detection. Furthermore, RIG-I-/- and MDA5-/- mice are highly susceptible to infection with these respective RNA viruses compared to control mice. Together, our data show that RIG-I and MDA5 distinguish different RNA viruses and are critical for host antiviral responses.
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“However, several RNA structural features have been described as immunostimulatory due to interactions with various RNA sensors such as Toll-like receptors, RIG-I, and PKR.”
From Sequence-engineered mRNA without chemical nucleoside modifications enables an effective protein therapy in large animals (2015) · cites this paper as [11]
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Pathogen Recognition and Innate Immunity
Akira, S., Uematsu, S., & Takeuchi, O. (2006) · Cell · doi:10.1016/j.cell.2006.02.015 · Cited by 11,976
Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3
Alexopoulou, L., Holt, A. C., Medzhitov, R., & Flavell, R. A. (2001) · Nature · doi:10.1038/35099560 · Cited by 6,129
Toll-like receptor control of the adaptive immune responses
Iwasaki, A., & Medzhitov, R. M. (2004) · Nature Immunology · doi:10.1038/ni1112 · Cited by 4,166
Yoneyama, M., Kikuchi, M., Natsukawa, T., Shinobu, N., Imaizumi, T., Miyagishi, M., Taira, K., Akira, S., & Fujita, T. (2004) · Nature Immunology · doi:10.1038/ni1087 · Cited by 4,022
Innate antiviral responses by means of TLR7-mediated recognition of single-stranded RNA
Diebold, S. S., Kaisho, T., Hemmi, H., Akira, S., & Reis e Sousa, C. (2004) · Science · doi:10.1126/science.1093616 · Cited by 3,444
Seth, R. B., Sun, L., Ea, C.-K., & Chen, Z. J. (2005) · Cell · doi:10.1016/j.cell.2005.08.012 · Cited by 3,329
Role of Adaptor TRIF in the MyD88-Independent Toll-Like Receptor Signaling Pathway
Yamamoto, M., Sato, S., Hemmi, H., Hoshino, K., Kaisho, T., Sanjo, H., Takeuchi, O., Sugiyama, M., Okabe, M., Takeda, K., et al. (2003) · Science · doi:10.1126/science.1087262 · Cited by 3,286
IKKε and TBK1 are essential components of the IRF3 signaling pathway
Fitzgerald, K. A., McWhirter, S. M., Faia, K. L., Rowe, D. C., Latz, E., Golenbock, D. T., Coyle, A. J., Liao, S.-M., & Maniatis, T. (2003) · Nature Immunology · doi:10.1038/ni921 · Cited by 2,680
IPS-1, an adaptor triggering RIG-I- and Mda5-mediated type I interferon induction
Kawai, T., Takahashi, K., Sato, S., Coban, C., Kumar, H., Kato, H., Ishii, K. J., Takeuchi, O., & Akira, S. (2005) · Nature Immunology · doi:10.1038/ni1243 · Cited by 2,562
Self-citationCardif is an adaptor protein in the RIG-I antiviral pathway and is targeted by hepatitis C virus
Meylan, E., Curran, J., Hofmann, K., Moradpour, D., Binder, M., Bartenschlager, R., & Tschopp, J. (2005) · Nature · doi:10.1038/nature04193 · Cited by 2,401
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The Long Unwinding Road of RNA Helicases
Bleichert, F., & Baserga, S. J. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.07.014 · Cited by 228
Innate immune sensing of coronavirus and viral evasion strategies
Kasuga, Y., Zhu, B., Jang, K., & Yoo, J. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00602-1 · Cited by 236
Understanding type 1 diabetes through genetics: advances and prospects
Polychronakos, C., & Li, Q. (2011) · Nature Reviews Genetics · doi:10.1038/nrg3069 · Cited by 226
Broquet, A. H., Hirata, Y., McAllister, C. S., & Kagnoff, M. F. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1002862 · Cited by 222
Brown, M. C., Holl, E. K., Boczkowski, D., Dobrikova, E. Y., Mosaheb, M., Chandramohan, V., Bigner, D. D., Gromeier, M., & Nair, S. K. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aan4220 · Cited by 228
Innate immune recognition of, and regulation by, DNA
Ishii, K. J., & Akira, S. (2006) · Trends in Immunology · doi:10.1016/j.it.2006.09.002 · Cited by 222
IPS-1 Is Essential for the Control of West Nile Virus Infection and Immunity
Suthar, M. S., Ma, D. Y., Thomas, S., Lund, J. M., Zhang, N., Daffis, S., Rudensky, A. Y., Bevan, M. J., Clark, E. A., Murali‐Krishna, K., et al. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000757 · Cited by 224
RIG-I-like receptors: Sensing and responding to RNA virus infection
Nakhaei, P., Génin, P., Civas, A., & Hiscott, J. B. (2009) · Seminars in Immunology · doi:10.1016/j.smim.2009.05.001 · Cited by 229
Toll-Like Receptors and Viruses: Induction of Innate Antiviral Immune Responses
Xagorari, A., & Chlichlia, K. (2008) · The Open Microbiology Journal · doi:10.2174/1874285800802010049 · Cited by 223
Two Years after Pandemic Influenza A/2009/H1N1: What Have We Learned?
Cheng, V. C., To, K. K., Tse, H., Hung, I. F., & Yuen, K. (2012) · Clinical Microbiology Reviews · doi:10.1128/cmr.05012-11 · Cited by 226
Intracellular Nucleic Acid Detection in Autoimmunity
Crowl, J. T., Gray, E. E., Pestal, K., Volkman, H. E., & Stetson, D. B. (2017) · Annual Review of Immunology · doi:10.1146/annurev-immunol-051116-052331 · Cited by 222
TLR7-dependent and FcγR-independent production of type I interferon in experimental mouse lupus
Lee, P. Y., Kumagai, Y., Li, Y., Takeuchi, O., Yoshida, H., Weinstein, J. S., Kellner, E. S., Nacionales, D. C., Barker, T. T., Kelly‐Scumpia, K. M., et al. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20080462 · Cited by 220
Distinct TLR- and NLR-Mediated Transcriptional Responses to an Intracellular Pathogen
Leber, J. H., Crimmins, G. T., Raghavan, S., Meyer-Morse, N., Cox, J. S., & Portnoy, D. A. (2008) · PLoS Pathogens · doi:10.1371/journal.ppat.0040006 · Cited by 226
Castanier, C., Zemirli, N., Portier, A., Garcin, D., Bidère, N., Vázquez, A., & Arnoult, D. (2012) · BMC Biology · doi:10.1186/1741-7007-10-44 · Cited by 216
Vaccine adjuvant uses of poly-IC and derivatives
Martins, K. A. O., Bavari, S., & Salazar, A. Μ. (2014) · Expert Review of Vaccines · doi:10.1586/14760584.2015.966085 · Cited by 221
Multiple roles of the coagulation protease cascade during virus infection
Antoniak, S., & Mackman, N. (2014) · Blood · doi:10.1182/blood-2013-09-526277 · Cited by 219
CD14 is a coreceptor of Toll-like receptors 7 and 9
Baumann, C., Aspalter, I. M., Sharif, O., Pichlmair, A., Blüml, S., Grebien, F., Brückner, M., Pasierbek, P., Aumayr, K., Planyavsky, M., et al. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20101111 · Cited by 220
SARS‐CoV‐2 sensing by RIG‐I and MDA5 links epithelial infection to macrophage inflammation
Thorne, L., Reuschl, A., Zuliani‐Alvarez, L., Whelan, M. V. X., Turner, J. L. E., Noursadeghi, M., Jolly, C. L., & Towers, G. J. (2021) · The EMBO Journal · doi:10.15252/embj.2021107826 · Cited by 223
Hayakawa, S., Shiratori, S., Yamato, H., Kameyama, T., Kitatsuji, C., Kashigi, F., Goto, S., Kameoka, S., Fujikura, D., Yamada, T., et al. (2010) · Nature Immunology · doi:10.1038/ni.1963 · Cited by 214
McCartney, S. A., Vermi, W., Gilfillan, S., Cella, M., Murphy, T. L., Schreiber, R. D., MURPHY, K. M. M., & Colonna, M. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20091181 · Cited by 222
A Virological View of Innate Immune Recognition
Iwasaki, A. (2012) · Annual Review of Microbiology · doi:10.1146/annurev-micro-092611-150203 · Cited by 230
Yan, J., Li, Q., Mao, A., Hu, M., & Shu, H. (2014) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mju005 · Cited by 218
DEAD/H BOX 3 (DDX3) helicase binds the RIG‐I adaptor IPS‐1 to up‐regulate IFN‐β‐inducing potential
Oshiumi, H., Sakai, K., Matsumoto, M., & Seya, T. (2010) · European Journal of Immunology · doi:10.1002/eji.200940203 · Cited by 216
Recognition of nucleic acids by pattern‐recognition receptors and its relevance in autoimmunity
Kawasaki, T., Kawai, T., & Akira, S. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01048.x · Cited by 226
Master sensors of pathogenic RNA – RIG-I like receptors
Schlee, M. (2013) · Immunobiology · doi:10.1016/j.imbio.2013.06.007 · Cited by 216
An origin of the immunogenicity of in vitro transcribed RNA
Mu, X., Greenwald, E., Ahmad, S., & Hur, S. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky177 · Cited by 218
Role of IFN regulatory factor 5 transcription factor in antiviral immunity and tumor suppression
Yanai, H., Chen, H.-M., Inuzuka, T., Kondo, S., Mak, T. W., Takaoka, A., Honda, K., & Taniguchi, T. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611559104 · Cited by 219
RIG-I is cleaved during picornavirus infection
Barral, P. M., Sarkar, D., Fisher, P. B., & Racaniello, V. R. (2009) · Virology · doi:10.1016/j.virol.2009.06.045 · Cited by 209
Wang, H., & Ryu, W. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000986 · Cited by 214
Enterovirus infections of the central nervous system
Rhoades, R. E., Tabor-Godwin, J. M., Tsueng, G., & Feuer, R. (2011) · Virology · doi:10.1016/j.virol.2010.12.014 · Cited by 213
Structural basis for dsRNA recognition and interferon antagonism by Ebola VP35
Leung, D. W., Prins, K. C., Borek, D., Farahbakhsh, M., Tufariello, J. M., Ramanan, P., Nix, J. C., Helgeson, L. A., Otwinowski, Z., Honzatko, R. B., et al. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1765 · Cited by 211
MAVS activates TBK1 and IKKε through TRAFs in NEMO dependent and independent manner
Fang, R., Jiang, Q., Zhou, X., Wang, C., Guan, Y., Tao, J., Xi, J., Feng, J., & Jiang, Z. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006720 · Cited by 218
Heer, A. K., Shamshiev, A. T., Donda, A., Uematsu, S., Akira, S., Köpf, M., & Marsland, B. J. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.4.2182 · Cited by 212
Lee‐Kirsch, M. A. (2016) · Annual Review of Medicine · doi:10.1146/annurev-med-050715-104506 · Cited by 216
Inn, K.-S., Gack, M. U., Tokunaga, F., Shi, M., Wong, L.-Y., Iwai, K., & Jung, J. U. (2011) · Molecular Cell · doi:10.1016/j.molcel.2010.12.029 · Cited by 209
Engineering patient-specific cancer immunotherapies
Scheetz, L., Park, K. S., Li, Q., Lowenstein, P. R., Castro, M. G., Schwendeman, A., & Moon, J. J. (2019) · Nature Biomedical Engineering · doi:10.1038/s41551-019-0436-x · Cited by 208
Field, R. H., Campion, S., Warren, C., Murray, C., & Cunningham, C. M. (2010) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2010.04.004 · Cited by 215
Wang, N., Liang, Y., Devaraj, S. G., Wang, J., Lemon, S. M., & Li, K. (2009) · Journal of Virology · doi:10.1128/jvi.01125-09 · Cited by 207
Pathogen recognition and Toll-like receptor targeted therapeutics in innate immune cells
Tartey, S., & Takeuchi, O. (2017) · International Reviews of Immunology · doi:10.1080/08830185.2016.1261318 · Cited by 209
Sykes, A., Edwards, M. R., Macintyre, J., del Rosario, A., Bakhsoliani, E., Trujillo‐Torralbo, M., Kon, O. M., Mallia, P., McHale, M. T., & Johnston, S. L. (2012) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2012.03.044 · Cited by 214
MDA5 cooperatively forms dimers and ATP‐sensitive filaments upon binding double‐stranded RNA
Berke, I. C., & Modis, Y. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.19 · Cited by 205
Identification and functions of pattern-recognition receptors
Kumagai, Y., & Akira, S. (2010) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2010.01.058 · Cited by 218
Bauhofer, O., Summerfield, A., Sakoda, Y., Tratschin, J.-D., Hofmann‐Apitius, M., & Ruggli, N. (2007) · Journal of Virology · doi:10.1128/jvi.02032-06 · Cited by 205
The DHX33 RNA Helicase Senses Cytosolic RNA and Activates the NLRP3 Inflammasome
Mitoma, H., Hanabuchi, S., Kim, T. I., Bao, M., Zhang, Z., Sugimoto, N., & Liu, Y. (2013) · Immunity · doi:10.1016/j.immuni.2013.07.001 · Cited by 204
How mRNA therapeutics are entering the monoclonal antibody field
Van Hoecke, L., & Roose, K. (2019) · Journal of Translational Medicine · doi:10.1186/s12967-019-1804-8 · Cited by 205
Kawashima, T., Kosaka, A., Yan, H., Guo, Z., Uchiyama, R., Fukui, R., Kaneko, D., Kumagai, Y., You, D., Carreras, J., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.02.024 · Cited by 206
Rajput, A., Kovalenko, A., Bogdanov, K., Yang, S., Kang, T., Kim, J., Du, J., & Wallach, D. (2011) · Immunity · doi:10.1016/j.immuni.2010.12.018 · Cited by 203
Lei, X., Liu, X., Ma, Y., Sun, Z., Yang, Y., Jin, Q., He, B., & Wang, J. (2010) · Journal of Virology · doi:10.1128/jvi.02491-09 · Cited by 205
Lung epithelial cells: therapeutically inducible effectors of antimicrobial defense
Leiva‐Juárez, M. M., Kolls, J. K., & Evans, S. E. (2017) · Mucosal Immunology · doi:10.1038/mi.2017.71 · Cited by 204
Myeloid heme oxygenase–1 regulates innate immunity and autoimmunity by modulating IFN-β production
Tzima, S., Victoratos, P., Kranidioti, K., Alexiou, M. V., & Kollias, G. A. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20081582 · Cited by 204
Aicardi-Goutières Syndrome Is Caused by IFIH1 Mutations
Oda, H., Nakagawa, K., Abe, J., Awaya, T., Funabiki, M., Hijikata, A., Nishikomori, R., Funatsuka, M., Ohshima, Y., Sugawara, Y., et al. (2014) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2014.06.007 · Cited by 203
Functions of the cytoplasmic RNA sensors RIG-I and MDA-5: Key regulators of innate immunity
Barral, P. M., Sarkar, D., Su, Z.-Z., Barber, G. N., DeSalle, R., Racaniello, V. R., & Fisher, P. B. (2009) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2009.06.012 · Cited by 201
Solution Structures of Cytosolic RNA Sensor MDA5 and LGP2 C-terminal Domains
Takahasi, K., Kumeta, H., Tsuduki, N., Narita, R., Shigemoto, T., Hirai, R., Yoneyama, M., Horiuchi, M., Ogura, K., Fujita, T., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.007179 · Cited by 196
Errett, J. S., Suthar, M. S., McMillan, A., Diamond, M., & Gale, M. (2013) · Journal of Virology · doi:10.1128/jvi.01488-13 · Cited by 201
RIG-I like receptors and their signaling crosstalk in the regulation of antiviral immunity
Ramos, H. J., & Gale, M. (2011) · Current Opinion in Virology · doi:10.1016/j.coviro.2011.04.004 · Cited by 202
Influenza virus activation of the interferon system
Killip, M. J., Fodor, E., & Randall, R. E. (2015) · Virus Research · doi:10.1016/j.virusres.2015.02.003 · Cited by 201
Solis, M., Nakhaei, P., Jalalirad, M., Lacoste, J., Douville, R. N., Arguello, M., Zhao, T., Laughrea, M., Wainberg, M. A., & Hiscott, J. B. (2010) · Journal of Virology · doi:10.1128/jvi.01635-10 · Cited by 198
Song, G., Liu, B., Li, Z., Wu, H. M., Wang, P., Zhao, K., Jiang, G., Zhang, L., & Gao, C. (2016) · Nature Immunology · doi:10.1038/ni.3588 · Cited by 201
Differential Recognition of TLR-Dependent Microbial Ligands in Human Bronchial Epithelial Cells
Mayer, A. K., Muehmer, M., Mages, J., Gueinzius, K., Hess, C., Heeg, K. M., Bals, R., Lang, R., & Dalpke, A. H. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.5.3134 · Cited by 202
Encephalomyocarditis Virus Viroporin 2B Activates NLRP3 Inflammasome
Ito, M., Yanagi, Y., & Ichinohe, T. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002857 · Cited by 199
Stahl‐Hennig, C., Eisenblätter, M., Jasny, E., Rzehak, T., Tenner‐Racz, K., Trumpfheller, C., Salazar, A. Μ., Überla, K., Nieto, K., Kleinschmidt, J. A., et al. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000373 · Cited by 199
Differential Inhibition of Type I Interferon Induction by Arenavirus Nucleoproteins
Martínez‐Sobrido, L., Giannakas, P., Cubitt, B., García‐Sastre, A., & de la Torre, J. C. (2007) · Journal of Virology · doi:10.1128/jvi.00882-07 · Cited by 198
Interferons: Signaling, antiviral and viral evasion
Bonjardim, C. A., Ferreira, P. C. P., & Kroon, E. G. (2009) · Immunology Letters · doi:10.1016/j.imlet.2008.11.002 · Cited by 196
Uhl, M., Kepp, O., Jusforgues-Saklani, H., Vicencio, J.-M., Kroemer, G., & Albert, M. L. (2009) · Cell Death & Differentiation · doi:10.1038/cdd.2009.8 · Cited by 196
Oshiumi, H., Miyashita, M., Matsumoto, M., & Seya, T. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003533 · Cited by 197
Rhinoviruses and Respiratory Enteroviruses: Not as Simple as ABC
Royston, L., & Tapparel, C. (2016) · Viruses · doi:10.3390/v8010016 · Cited by 215
Severe influenza pneumonitis in children with inherited TLR3 deficiency
Lim, H. K., Huang, S. X. L., Chen, J., Kerner, G., Gilliaux, O., Bastard, P., Dobbs, K., Hernandez, N., Goudin, N., Hasek, M. L., et al. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20181621 · Cited by 202
Biological and social aspects of Coronavirus Disease 2019 (COVID-19) related to oral health
Pereira, L. J., Pereira, C. V., Murata, R. M., Pardi, V., & Pereira, S. M. (2020) · Brazilian Oral Research · doi:10.1590/1807-3107bor-2020.vol34.0041 · Cited by 205
Theoretical basis for stabilizing messenger RNA through secondary structure design
Wayment-Steele, H. K., Kim, D. S., Choe, C. A., Nicol, J. J., Wellington-Oguri, R., Watkins, A. M., Parra Sperberg, R. A., Huang, P.-S., Participants, E., & Das, R. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab764 · Cited by 197
Mechanisms of MAVS Regulation at the Mitochondrial Membrane
Jacobs, J. L., & Coyne, C. B. (2013) · Journal of Molecular Biology · doi:10.1016/j.jmb.2013.10.007 · Cited by 203
Wang, Y., Shaked, I., Stanford, S. M., Zhou, W., Curtsinger, J., Mikulski, Z., Shaheen, Z. R., Cheng, G., Sawatzke, K., Campbell, A. M., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.06.013 · Cited by 194
Chicken Cells Sense Influenza A Virus Infection through MDA5 and CARDIF Signaling Involving LGP2
Liniger, M., Summerfield, A., Zimmer, G., McCullough, K. C., & Ruggli, N. (2011) · Journal of Virology · doi:10.1128/jvi.00742-11 · Cited by 203
The tumor suppressor PTEN has a critical role in antiviral innate immunity
Li, S., Zhu, M., Pan, R., Fang, T., Cao, Y., Chen, S., Zhao, X., Lei, C., Guo, L., Chen, Y. Z., et al. (2015) · Nature Immunology · doi:10.1038/ni.3311 · Cited by 195
Daffis, S., Samuel, M. A., Keller, B. C., Gale, M., & Diamond, M. (2007) · PLoS Pathogens · doi:10.1371/journal.ppat.0030106 · Cited by 194
Tumor-derived exosomes antagonize innate antiviral immunity
Gao, L., Wang, L., Dai, T., Jin, K., Zhang, Z., Wang, S., Xie, F., Fang, P., Yang, B., Huang, H., et al. (2018) · Nature Immunology · doi:10.1038/s41590-017-0043-5 · Cited by 195
Genetic analysis of resistance to viral infection
Beutler, B., Eidenschenk, C., Crozat, K., Imler, J., Takeuchi, O., Hoffmann, J. A., & Akira, S. (2007) · Nature reviews. Immunology · doi:10.1038/nri2174 · Cited by 190
MDA-5 Is Cleaved in Poliovirus-Infected Cells
Barral, P. M., Morrison, J. M., Drahos, J., Gupta, P., Sarkar, D., Fisher, P. B., & Racaniello, V. R. (2007) · Journal of Virology · doi:10.1128/jvi.01360-06 · Cited by 192
ZBP1/DAI ubiquitination and sensing of influenza vRNPs activate programmed cell death
Kesavardhana, S., Kuriakose, T., Guy, C. S., Samir, P., Malireddi, R. K. S., Mishra, A., & Kanneganti, T. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20170550 · Cited by 195
Atkinson, N. J., Witteveldt, J., Evans, D. J., & Simmonds, P. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku075 · Cited by 192
Macrophage and dendritic cell phenotypic diversity in the context of biomaterials
Kou, P. M., & Babensee, J. E. (2011) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.32971 · Cited by 190
Ubiquitination in the antiviral immune response
Davis-Gardner, M. E., & Gack, M. U. (2015) · Virology · doi:10.1016/j.virol.2015.02.033 · Cited by 197
Weber, M., Gawanbacht, A., Habjan, M., Rang, A., Borner, C., Schmidt, A. M., Veitinger, S., Jacob, R., Devignot, S., Kochs, G., et al. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.01.012 · Cited by 190
Silencing or Stimulation? siRNA Delivery and the Immune System
Whitehead, K. A., Dahlman, J. E., Langer, R., & Anderson, D. G. (2011) · Annual Review of Chemical and Biomolecular Engineering · doi:10.1146/annurev-chembioeng-061010-114133 · Cited by 200
Melén, K., Kinnunen, L., Fagerlund, R., Ikonen, N., Twu, K. Y., Krug, R. M., & Julkunen, I. (2007) · Journal of Virology · doi:10.1128/jvi.01714-06 · Cited by 190
Response of host inflammasomes to viral infection
Chen, I.-Y., & Ichinohe, T. (2014) · Trends in Microbiology · doi:10.1016/j.tim.2014.09.007 · Cited by 198
Johnsen, I. B., Nguyen, T. T., Ringdal, M., Tryggestad, A. M. A., Bakke, O., Lien, E., Espevik, T., & Anthonsen, M. W. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601222 · Cited by 192
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Metadata
- Authors
- Kato, H., Takeuchi, O., Sato, S., Yoneyama, M., Yamamoto, M., Matsui, K., Uematsu, S., Jung, A., Kawai, T., Ishii, K. J., Yamaguchi, O., Otsu, K., Tsujimura, T., Koh, C.-S., Reis e Sousa, C., Matsuura, Y., Fujita, T., & Akira, S.
- Affiliations
- Research Institute for Microbial Diseases, The University of Osaka (JP)
- Japan Science and Technology Agency (JP)
- Kyoto University (JP)
- The University of Osaka (JP)
- Hyogo Medical University (JP)
- Shinshu University (JP)
- Corresponding author
- Akira, Shizuo
- ORCID
- Venue
- Nature
- Published
- 2006-04-09
- Volume
- 441
- Issue
- 7089
- Pages
- 101-105
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2028575270
- Cited by
- 3,888
- References
- 28
- Citations by year
- 2026: 143 · 2025: 156 · 2024: 146 · 2023: 163 · 2022: 176 · 2021: 204 · 2020: 182 · 2019: 169 · 2018: 169 · 2017: 175 · 2016: 169 · 2015: 182 · 2014: 233 · 2013: 218 · 2012: 236
- FWCI
- 88.17
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
- Keywords
- MDA5, RIG-I, double-stranded RNA recognition, antiviral innate immunity, interferon production, poly(I:C), paramyxovirus, influenza virus, Japanese encephalitis virus, picornavirus, viral susceptibility
- MeSH terms
- DEAD Box Protein 58, Interferon-Induced Helicase, IFIH1, Animals, Encephalitis Virus, Japanese, Encephalomyocarditis virus, Immunity, Innate, RNA Viruses, RNA, Double-Stranded, RNA, Viral, RNA Helicases, Mice, DEAD-box RNA Helicases
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