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STING is an endoplasmic reticulum adaptor that facilitates innate immune signalling
Open accessAbstract
The cellular innate immune system is essential for recognizing pathogen infection and for establishing effective host defence. But critical molecular determinants responsible for facilitating an appropriate immune response-following infection with DNA and RNA viruses, for example-remain to be identified. Here we report the identification, following expression cloning, of a molecule (STING; stimulator of interferon genes) that appears essential for effective innate immune signalling processes. It comprises five putative transmembrane regions, predominantly resides in the endoplasmic reticulum and is able to activate both NF-kappaB and IRF3 transcription pathways to induce expression of type I interferon (IFN-alpha and IFN-beta ) and exert a potent anti-viral state following expression. In contrast, loss of STING rendered murine embryonic fibroblasts extremely susceptible to negative-stranded virus infection, including vesicular stomatitis virus. Further, STING ablation abrogated the ability of intracellular B-form DNA, as well as members of the herpesvirus family, to induce IFN-beta, but did not significantly affect the Toll-like receptor (TLR) pathway. Yeast two-hybrid and co-immunoprecipitation studies indicated that STING interacts with RIG-I and with SSR2 (also known as TRAPbeta), which is a member of the translocon-associated protein (TRAP) complex required for protein translocation across the endoplasmic reticulum membrane following translation. Ablation by RNA interference of both TRAPbeta and translocon adaptor SEC61beta was subsequently found to inhibit STING's ability to stimulate expression of IFN-beta. Thus, as well as identifying a regulator of innate immune signalling, our results imply a potential role for the translocon in innate signalling pathways activated by select viruses as well as intracellular DNA.
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“TBK1 also activates NF‐κB to induce expression of IFN and inflammatory cytokines.65, 66, 67”
From Cellular senescence and senescence-associated secretory phenotype via the cGAS-STING signaling pathway in cancer (2020) · cites this paper as [65]
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“cGAMP produced by cGAS activation binds to STING which is located on the membrane of endoplasmic reticulum (ER)391 and leads to the translocation of STING from ER to the Golgi where it is further modified.392”
From Role of neuroinflammation in neurodegeneration development (2023) · cites this paper as [391]
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“the stimulator of interferon genes (STING) has been shown to be a major pathway for the detection of immunogenic tumors and initiation of a spontaneous T cell response18–21.”
From Epigenetic state determines the in vivo efficacy of STING agonist therapy (2023) · cites this paper as [20]
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“TBK1 associated with STING also facilitates dsDNA-mediated activation of NF-κB to promote proinflammatory gene transcription (Abe and Barber, 2014; Ishikawa and Barber, 2008).”
From Cytoplasmic DNA: sources, sensing, and role in aging and disease (2021) · cites this paper as Ishikawa and Barber, 2008
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Cites
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
Differential roles of MDA5 and RIG-I helicases in the recognition of RNA viruses
Kato, H., Takeuchi, O., Sato, S., Yoneyama, M., Yamamoto, M., Matsui, K., Uematsu, S., Jung, A., Kawai, T., Ishii, K. J., et al. (2006) · Nature · doi:10.1038/nature04734 · Cited by 3,888
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
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
5'-Triphosphate RNA Is the Ligand for RIG-I
Hornung, V., Ellegast, J., Kim, S., Brzózka, K., Jung, A., Kato, H., Poeck, H., Akira, S., Conzelmann, K.-K., Schlee, M., et al. (2006) · Science · doi:10.1126/science.1132505 · Cited by 2,474
Cardif 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
RIG-I-mediated antiviral responses to single-stranded RNA bearing 5’-phosphates
Pichlmair, A., Schulz, O., Tan, C. P., Näslund, T. I., Liljeström, P., Weber, F., & Reis e Sousa, C. (2006) · Science · doi:10.1126/science.1132998 · Cited by 2,210
VISA Is an Adapter Protein Required for Virus-Triggered IFN-β Signaling
Xu, L., Wang, Y., Han, K.-J., Li, L., Zhai, Z., & Shu, H. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.08.014 · Cited by 1,849
Distinct RIG-I and MDA5 Signaling by RNA Viruses in Innate Immunity
Loo, Y.-M., Fornek, J., Crochet, N., Bajwa, G., Perwitasari, O., Martinez-Sobrido, L., Akira, S., Gill, M. A., García-Sastre, A., Katze, M. G., et al. (2008) · Journal of Virology · doi:10.1128/jvi.01080-07 · Cited by 1,071
Recognition of Cytosolic DNA Activates an IRF3-Dependent Innate Immune Response
Stetson, D. B., & Medzhitov, R. M. (2006) · Immunity · doi:10.1016/j.immuni.2005.12.003 · Cited by 1,003
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Lei, Y. L., Wen, H., Yu, Y., Taxman, D. J., Zhang, L., Widman, D. G., Swanson, K. V., Wen, K. W., Damania, B., Moore, C., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.03.025 · Cited by 297
STING Recognition of Cytoplasmic DNA Instigates Cellular Defense
Abe, T., Harashima, A., Xia, T., Konno, H., Konno, K., Morales, A. A., Ahn, J., Gutman, D. M., & Barber, G. N. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.01.039 · Cited by 311
Self-citationMitochondrial shape changes: orchestrating cell pathophysiology
Campello, S., & Scorrano, L. (2010) · EMBO Reports · doi:10.1038/embor.2010.115 · Cited by 307
Zhang, D., Liu, Y., Zhu, Y., Zhang, Q. Y., Guan, H., Liu, S., Chen, S., Chen, M., Chen, C., Liao, Z., et al. (2022) · Nature Cell Biology · doi:10.1038/s41556-022-00894-z · Cited by 301
The function and clinical application of extracellular vesicles in innate immune regulation
Zhou, X., Xie, F., Wang, L., Zhang, L., Zhang, S., Fang, M., & Zhou, F. (2020) · Cellular & Molecular Immunology · doi:10.1038/s41423-020-0391-1 · Cited by 294
Intrinsic antiproliferative activity of the innate sensor STING in T lymphocytes
Cerboni, S., Jeremiah, N., Gentili, M., Gehrmann, U., Conrad, C., Stolzenberg, M., Pïcard, C., Neven, B., Fischer, A., Amigorena, S., et al. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20161674 · Cited by 303
The Antiviral Innate Immune Response in Fish: Evolution and Conservation of the IFN System
Langevin, C., Aleksejeva, E., Passoni, G., Palha, N., Levraud, J., & Boudinot, P. (2013) · Journal of Molecular Biology · doi:10.1016/j.jmb.2013.09.033 · Cited by 299
STING inhibitors target the cyclic dinucleotide binding pocket
Hong, Z., Mei, J., Li, C., Bai, G., Maimaiti, M., Hu, H., Yu, W., Sun, L., Zhang, L., Cheng, D., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2105465118 · Cited by 296
Cancer-Cell-Intrinsic cGAS Expression Mediates Tumor Immunogenicity
Schadt, L., Sparano, C., Schweiger, N. A., Siliņa, K., Cecconi, V., Lucchiari, G., Yagita∥, H., Guggisberg, E., Saba, S., Naščáková, Z., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.09.065 · Cited by 299
Trial watch: STING agonists in cancer therapy
Le Naour, J., Zitvogel, L., Galluzzi, L., Vacchelli, E., & Kroemer, G. (2020) · OncoImmunology · doi:10.1080/2162402x.2020.1777624 · Cited by 289
The flavivirus NS2B–NS3 protease–helicase as a target for antiviral drug development
Luo, D., Vasudevan, S. G., & Lescar, J. (2015) · Antiviral Research · doi:10.1016/j.antiviral.2015.03.014 · Cited by 295
Zhou, C., Chen, X., Planells‐Cases, R., Chu, J., Wang, L., Cao, L., Li, Z., López‐Cayuqueo, K. I., Xie, Y., Ye, S., et al. (2020) · Immunity · doi:10.1016/j.immuni.2020.03.016 · Cited by 295
Cytoplasmic DNA: sources, sensing, and role in aging and disease
Miller, K. N., Victorelli, S. G., Salmonowicz, H., Dasgupta, N., Liu, T., Passos, J. F., & Adams, P. D. (2021) · Cell · doi:10.1016/j.cell.2021.09.034 · Cited by 288
Fensterl, V., & Sen, G. C. (2010) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2010.0101 · Cited by 288
Regulation of cGAS–STING signalling and its diversity of cellular outcomes
Zhang, Z., & Zhang, C. (2025) · Nature Reviews Immunology · doi:10.1038/s41577-024-01112-7 · Cited by 287
Luo, W., Wang, Y., Zhang, L., Ren, P., Zhang, C., Li, Y., Azares, A. R., Zhang, M. H., Guo, J., Ghaghada, K. B., et al. (2019) · Circulation · doi:10.1161/circulationaha.119.041460 · Cited by 289
Jin, L., Hill, K. K., Filak, H. C., Mogan, J., Knowles, H. M., Zhang, B., Perraud, A., Cambier, J. C., & Lenz, L. L. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100088 · Cited by 285
Rao, Y., & Su, J. (2015) · Journal of Immunology Research · doi:10.1155/2015/670437 · Cited by 285
Olagnier, D., Brandtoft, A. M., Gunderstofte, C., Villadsen, N. L., Krapp, C., Thielke, A. L., Laustsen, A., Peri, S., Hansen, A. L., Bonefeld, L., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05861-7 · Cited by 282
Barber, G. N. (2011) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.12.015 · Cited by 287
Self-citationZhang, L., Mo, J., Swanson, K. V., Wen, H., Petrucelli, A., Gregory, S. M., Zhang, Z., Schneider, M., Jiang, Y., Fitzgerald, K. A., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.01.010 · Cited by 283
Cyclic di-GMP Sensing via the Innate Immune Signaling Protein STING
Yin, Q., Tian, Y., Kabaleeswaran, V., Jiang, X., Tu, D., Eck, M. J., Chen, Z. J., & Wu, H. (2012) · Molecular Cell · doi:10.1016/j.molcel.2012.05.029 · Cited by 293
The Role of Interferons in Inflammation and Inflammasome Activation
Kopitar-Jerala, N. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00873 · Cited by 260
Molecular regulation of interferon antiviral response in fish
Zhang, Y.-B., & Gui, J. (2012) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2012.06.003 · Cited by 279
Casadio, M., Ciancanelli, M. J., Ou, Y.-H., Lorenzo, L., Klaudel‐Dreszler, M., Pauwels, E., Sancho‐Shimizu, V., de Diego, R. P., Abhyankar, A., Israelsson, E., et al. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20111316 · Cited by 292
Cytosolic DNA sensing by cGAS: regulation, function, and human diseases
Yu, L., & Liu, P. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00554-y · Cited by 295
Wang, Y., Ning, X., Gao, P., Wu, S., Sha, M., Lv, M., Zhou, X., Gao, J., Fang, R., Meng, G., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.02.011 · Cited by 279
Evolutionary Origins of cGAS-STING Signaling
Margolis, S. R., Wilson, S. C., & Vance, R. E. (2017) · Trends in Immunology · doi:10.1016/j.it.2017.03.004 · Cited by 282
Gajewski, T. F., Corrales, L. P., Williams, J. B., Horton, B. L., Sivan, A., & Spranger, S. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-67577-0_2 · Cited by 284
The Cyclopeptide Astin C Specifically Inhibits the Innate Immune CDN Sensor STING
Li, S., Hong, Z., Wang, Z., Li, F., Mei, J., Huang, L., Lou, X., Zhao, S., Song, L., Chen, W., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.11.097 · Cited by 279
Yi, G., Brendel, V., Shu, C., Li, P., Palanathan, S., & Kao, C. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077846 · Cited by 283
Innate Immune Recognition in Infectious and Noninfectious Diseases of the Lung
Opitz, B., van Laak, V., Eitel, J., & Suttorp, N. (2010) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200909-1427so · Cited by 287
Konno, H., Yamauchi, S., Berglund, A., Putney, R. M., Mulé, J. J., & Barber, G. N. (2018) · Oncogene · doi:10.1038/s41388-017-0120-0 · Cited by 281
Self-citationWu, S., Zhang, Q., Zhang, F., Meng, F., Liu, S., Zhou, R., Wu, Q., Li, X., Shen, L., Huang, J., et al. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0352-z · Cited by 278
Chen, X., Yang, X., Zheng, Y., Yang, Y., Xing, Y., & Chen, Z. (2014) · Protein & Cell · doi:10.1007/s13238-014-0026-3 · Cited by 272
Meric‐Bernstam, F., Sweis, R. F., Kasper, S., Hamid, O., Bhatia, S., Dummer, R., Stradella, A., Long, G. V., Spreafico, A., Shimizu, T., et al. (2022) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-22-2235 · Cited by 281
The STING pathway and the T cell-inflamed tumor microenvironment
Woo, S., Corrales, L. P., & Gajewski, T. F. (2015) · Trends in Immunology · doi:10.1016/j.it.2015.02.003 · Cited by 275
Research Advances in How the cGAS-STING Pathway Controls the Cellular Inflammatory Response
Wan, D., Jiang, W., & Hao, J. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00615 · Cited by 270
Sun, L., Xing, Y., Chen, X., Zheng, Y., Yang, Y., Nichols, D. B., Clementz, M. A., Banach, B. S., Li, K., Baker, S. C., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030802 · Cited by 269
The IRF Family Transcription Factors at the Interface of Innate and Adaptive Immune ResponsesPreprint
Ikushima, H., Negishi, H., & Taniguchi, T. (2013) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2013.78.020321 · Cited by 273
Dampened STING-Dependent Interferon Activation in Bats
Xie, J., Li, Y., Shen, X.-R., Goh, G., Zhu, Y., Cui, J., Wang, L., Shi, Z., & Zhou, P. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.01.006 · Cited by 277
Yan, M., Li, Y., Luo, Q., Zeng, W., Shao, X., Li, L., Wang, Q., Wang, D., Zhang, Y., Diao, H., et al. (2022) · Cell Death Discovery · doi:10.1038/s41420-022-01046-w · Cited by 267
Positive Regulation of Interferon Regulatory Factor 3 Activation by Herc5 via ISG15 Modification
Shi, H.-X., Yang, K. S., Liu, X., Liu, X.-Y., Wei, B., Shan, Y.-F., Zhu, L.-H., & Wang, C. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.01466-09 · Cited by 274
Oshiumi, H., Miyashita, M., Inoue, N., Okabe, M., Matsumoto, M., & Seya, T. (2010) · Cell Host & Microbe · doi:10.1016/j.chom.2010.11.008 · Cited by 264
Fish MITA Serves as a Mediator for Distinct Fish IFN Gene Activation Dependent on IRF3 or IRF7
Sun, F., Zhang, Y.-B., Liu, T., Shi, J., Wang, B., & Gui, J. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100642 · Cited by 263
Cheng, N., Watkins-Schulz, R., Junkins, R. D., David, C. N., Johnson, B. M., Montgomery, S. A., Peine, K. J., Darr, D. B., Yuan, H., McKinnon, K. P., et al. (2018) · JCI Insight · doi:10.1172/jci.insight.120638 · Cited by 267
Jiang, H., Xue, X., Panda, S., Kawale, A. S., Hooy, R. M., Liang, F., Sohn, J., Sung, P., & Gekara, N. O. (2019) · The EMBO Journal · doi:10.15252/embj.2019102718 · Cited by 270
Cyclic GMP–AMP as an Endogenous Second Messenger in Innate Immune Signaling by Cytosolic DNA
Kato, K., Omura, H., Ishitani, R., & Nureki, O. (2017) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-061516-044813 · Cited by 265
Toll-Like Receptors: General Molecular and Structural Biology
Behzadi, P., García‐Perdomo, H. A., & Karpiński, T. M. M. (2021) · Journal of Immunology Research · doi:10.1155/2021/9914854 · Cited by 267
Innate Immune Recognition of an AT-Rich Stem-Loop DNA Motif in the Plasmodium falciparum Genome
Sharma, S., DeOliveira, R. B., Kalantari, P., Parroche, P., Goutagny, N., Jiang, Z., Chan, J., Bartholomeu, D. C., Lauw, F. N., Hall, J. P., et al. (2011) · Immunity · doi:10.1016/j.immuni.2011.05.016 · Cited by 258
Self-citationSTING activation in cancer immunotherapy
Su, T., Zhang, Y. L., Valerie, K. C., Wang, X., Lin, S., & Zhu, G. (2019) · Theranostics · doi:10.7150/thno.37574 · Cited by 262
Dengue Virus Targets the Adaptor Protein MITA to Subvert Host Innate Immunity
Yu, C.-Y., Chang, T.-H., Liang, J., Chiang, R.-L., Lee, Y.-L., Liao, C., & Lin, Y. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002780 · Cited by 257
The STING1 network regulates autophagy and cell death
Zhang, R., Kang, R., & Tang, D. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00613-4 · Cited by 266
Hu, X., Zhang, H., Zhang, Q., Yao, X. X., Ni, W., & Zhou, K. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02602-y · Cited by 271
Mitofusin 2 Inhibits Mitochondrial Antiviral Signaling
Yasukawa, K., Oshiumi, H., Takeda, M., Ishihara, N., Yanagi, Y., Seya, T., Kawabata, S.-I., & Koshiba, T. (2009) · Science Signaling · doi:10.1126/scisignal.2000287 · Cited by 255
STING controls nociception via type I interferon signalling in sensory neurons
Donnelly, C. R., Jiang, C., Andriessen, A. S., Wang, K., Wang, Z., Ding, H., Zhao, J., Luo, X., Lee, M. S., Lei, Y. L., et al. (2021) · Nature · doi:10.1038/s41586-020-03151-1 · Cited by 262
Viruses transfer the antiviral second messenger cGAMP between cells
Bridgeman, A., Maelfait, J., Davenne, T., Partridge, T., Peng, Y., Mayer, A., Dong, T., Kaever, V., Borrow, P., & Rehwinkel, J. (2015) · Science · doi:10.1126/science.aab3632 · Cited by 261
Ohkuri, T., Ghosh, A., Kosaka, A., Zhu, J., Ikeura, M., David, M., Watkins, S. C., Sarkar, S. N., & Okada, H. (2014) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-14-0099 · Cited by 255
STING inhibits the reactivation of dormant metastasis in lung adenocarcinoma
Hu, J. Y., Rivera, F. J. S., Wang, Z., Johnson, G. N., Ho, Y.-J., Ganesh, K., Umeda, S., Gan, S., Mujal, A. M., Delconte, R. B., et al. (2023) · Nature · doi:10.1038/s41586-023-05880-5 · Cited by 261
Cytosolic DNA Sensing in Organismal Tumor Control
Vanpouille-Box, C., Demaria, S., Formenti, S. C., & Galluzzi, L. (2018) · Cancer Cell · doi:10.1016/j.ccell.2018.05.013 · Cited by 250
Ancient Origin of cGAS-STING Reveals Mechanism of Universal 2′,3′ cGAMP Signaling
Kranzusch, P. J., Wilson, S. C., Lee, A. S. Y., Berger, J. M., Doudna, J. A., & Vance, R. E. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.07.022 · Cited by 256
Cytoplasmic DNA innate immune pathways
Barber, G. N. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01051.x · Cited by 253
Self-citationVirus-cell fusion as a trigger of innate immunity dependent on the adaptor STING
Holm, C. K., Jensen, S. B., Jakobsen, M. R., Cheshenko, N., Horan, K., Moeller, H. B., Gonzalez‐Dosal, R., Rasmussen, S. B., Christensen, M. H., Yarovinsky, T. O., et al. (2012) · Nature Immunology · doi:10.1038/ni.2350 · Cited by 253
Luo, W., Li, S., Li, C., Lian, H., Yang, Q., Zhong, B., & Shu, H. (2016) · Nature Immunology · doi:10.1038/ni.3510 · Cited by 249
Mitochondria in innate immunity
Arnoult, D., Soares, F., Tattoli, I., & Girardin, S. E. (2011) · EMBO Reports · doi:10.1038/embor.2011.157 · Cited by 256
Zhang, Z., Bao, M., Lu, N., Weng, L., Yuan, B., & Liu, Y. (2012) · Nature Immunology · doi:10.1038/ni.2492 · Cited by 249
Regulation of innate immune responses by autophagy-related proteins
Saitoh, T., & Akira, S. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201002021 · Cited by 251
Structural basis for the inhibition of cGAS by nucleosomes
Kujirai, T., Zierhut, C., Takizawa, Y., Kim, R., Negishi, L., Uruma, N., Hirai, S., Funabiki, H., & Kurumizaka, H. (2020) · Science · doi:10.1126/science.abd0237 · Cited by 243
Belgnaoui, S. M., Paz, S., & Hiscott, J. B. (2011) · Current Opinion in Immunology · doi:10.1016/j.coi.2011.08.001 · Cited by 241
Qiao, J. T., Cui, C., Qing, L., Wang, L., He, T., Yan, F., Liu, F. Q., Shen, Y. H., Hou, X., & Chen, L. (2017) · Metabolism · doi:10.1016/j.metabol.2017.09.010 · Cited by 245
STING mediates neurodegeneration and neuroinflammation in nigrostriatal α-synucleinopathy
Hinkle, J. T., Patel, J., Panicker, N., Karuppagounder, S. S., Biswas, D., Belingon, B., Chen, R., Brahmachari, S., Pletnikova, O., Troncoso, J. C., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2118819119 · Cited by 240
Liu, Y., Gordesky-Gold, B., Leney-Greene, M. A., Weinbren, N. L., Tudor, M., & Cherry, S. R. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.05.022 · Cited by 244
Wang, W., Hu, D., Feng, Y., Wu, J., Li, A., Wang, Y., Cheng, K., Tian, M., Xiao, F., Zhang, Q., et al. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008335 · Cited by 240
Trial watch: TLR3 agonists in cancer therapy
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Organelle-specific initiation of cell death
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The interferon response to intracellular DNA: Why so many receptors?
Unterholzner, L. (2013) · Immunobiology · doi:10.1016/j.imbio.2013.07.007 · Cited by 248
Structural basis of nucleosome-dependent cGAS inhibition
Boyer, J. A., Spangler, C. J., Strauss, J. D., Cesmat, A. P., Liu, P., McGinty, R. K., & Zhang, Q. (2020) · Science · doi:10.1126/science.abd0609 · Cited by 238
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Phosphorylation and chromatin tethering prevent cGAS activation during mitosis
Li, T., Huang, T., Du, M., Chen, X., Du, F., Ren, J., & Chen, Z. J. (2021) · Science · doi:10.1126/science.abc5386 · Cited by 247
Barker, J. R., Koestler, B. J., Carpenter, V. K., Burdette, D. L., Waters, C. M., Vance, R. E., & Valdivia, R. H. (2013) · mBio · doi:10.1128/mbio.00018-13 · Cited by 248
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Stegmann, M., Anderson, R. G., Ichimura, K., Pečenková, T., Reuter, P., Žárský, V., McDowell, J. M., Shirasu, K., & Trujillo, M. (2012) · The Plant Cell · doi:10.1105/tpc.112.104463 · Cited by 234
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Metadata
- Authors
- Ishikawa, H., & Barber, G. N.
- Affiliations
- University of Miami (US)
- Corresponding author
- Barber, Glen N.
- Venue
- Nature
- Published
- 2008-08-24
- Volume
- 455
- Issue
- 7213
- Pages
- 674-678
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC2804933
- OpenAlex
- W2060004514
- Semantic Scholar
- cd831bfb6fd9847baedbe5161ddd21d405728bee
- Cited by
- 3,576
- References
- 29
- Citations by year
- 2026: 310 · 2025: 394 · 2024: 359 · 2023: 332 · 2022: 322 · 2021: 315 · 2020: 270 · 2019: 195 · 2018: 163 · 2017: 161 · 2016: 115 · 2015: 118 · 2014: 112 · 2013: 123 · 2012: 83
- FWCI
- 28.23
- Type
- journal article
- Language
- en
- Update notices
- erratum (2008-11-13)
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases (R01AI079336)
- 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 › Cell Biology › Endoplasmic Reticulum Stress and Disease
- Keywords
- STING, endoplasmic reticulum, innate immunity, interferon-beta, IRF3, NF-κB, RIG-I, Sec61β, translocon, TRAP complex, vesicular stomatitis virus, herpesvirus, negative-strand RNA viruses, viral DNA sensing, antiviral defense, protein translocation, pattern recognition receptors
- MeSH terms
- STING Protein, Animals, Cell Line, Endoplasmic Reticulum, Fibroblasts, Humans, Immunity, Innate, Interferons, Membrane Proteins, Mice, Inbred C57BL, Signal Transduction, Mice, Knockout, Mice
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