The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
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.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“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]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“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]
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“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]
Experimental — accuracy not yet measuredIn the citing paper
“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
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
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
Cited by
Sorted by citations
Items 301–400 of 1,005
NEMO–IKKβ Are Essential for IRF3 and NF-κB Activation in the cGAS–STING Pathway
Fang, R., Wang, C., Jiang, Q., Lv, M., Gao, P., Yu, X., Mu, P., Zhang, R., Bi, S., Feng, J., et al. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1700699 · Cited by 227
Tsourouktsoglou, T.-D., Warnatsch, A., Ιωάννου, Μ., Hoving, D., Wang, Q., & Papayannopoulos, V. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107602 · Cited by 227
Adenovirus Detection by the cGAS/STING/TBK1 DNA Sensing Cascade
Lam, E., Stein, S. C., & Falck-Pedersen, E. (2013) · Journal of Virology · doi:10.1128/jvi.02702-13 · Cited by 236
STING Signaling Promotes Inflammation in Experimental Acute Pancreatitis
Zhao, Q., Wei, Y., Pandol, S. J., Li, L., & Habtezion, A. (2018) · Gastroenterology · doi:10.1053/j.gastro.2018.01.065 · Cited by 225
TBK1 Directly Engages Akt/PKB Survival Signaling to Support Oncogenic Transformation
Ou, Y.-H., Torres, M. J., Ram, R. R., Formstecher, É., Roland, C. L., Cheng, T., Brekken, R. A., Wurz, R. P., Tasker, A. S., Polverino, T., et al. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.01.019 · Cited by 224
The PYHIN protein family as mediators of host defenses
Schattgen, S., & Fitzgerald, K. A. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01053.x · Cited by 224
Immunogenetics of systemic lupus erythematosus: A comprehensive review
Ghodke‐Puranik, Y., & Niewold, T. B. (2015) · Journal of Autoimmunity · doi:10.1016/j.jaut.2015.08.004 · Cited by 223
Extensive evolutionary and functional diversity among mammalian AIM2-like receptors
Brunette, R. L., Young, J. M., Whitley, D. G., Brodsky, I. E., Malik, H. S., & Stetson, D. B. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20121960 · Cited by 230
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
Human STING is a proton channel
Liu, B., Carlson, R. J., Pires, I. S., Gentili, M., Feng, E., Hellier, Q., Schwartz, M. A., Blainey, P. C., Irvine, D. J., & Hacohen, N. (2023) · Science · doi:10.1126/science.adf8974 · Cited by 223
Prantner, D., Perkins, D. J., Lai, W., Williams, M. S., Sharma, S., Fitzgerald, K. A., & Vogel, S. N. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.382986 · Cited by 225
Mitochondrial dysfunction and the AKI-to-CKD transition
Jiang, M., Bai, M., Lei, J., Xie, Y., Xu, S., Jia, Z., & Zhang, A. (2020) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00285.2020 · Cited by 224
Modular Architecture of the STING C-Terminal Tail Allows Interferon and NF-κB Signaling Adaptation
Mann, C. C. D. O., Orzalli, M. H., King, D., Kagan, J. C., Lee, A. S. Y., & Kranzusch, P. J. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.03.098 · Cited by 226
Mohamed, E. T., Sierra, R. A., Trillo-Tinoco, J., Cao, Y. W., Innamarato, P., Payne, K. K., Pulido, Á. D. M., Mandula, J. K., Zhang, S., Thevenot, P., et al. (2020) · Immunity · doi:10.1016/j.immuni.2020.03.004 · Cited by 223
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
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
Innate immune recognition of DNA: A recent history
Dempsey, A., & Bowie, A. (2015) · Virology · doi:10.1016/j.virol.2015.03.013 · Cited by 229
Zhang, Z., Zhou, H., Ouyang, X., Dong, Y., Sarapultsev, A., Luo, S., & Hu, D. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01252-z · Cited by 222
Structure and Ubiquitination-Dependent Activation of TANK-Binding Kinase 1
Tu, D., Zhu, Z., Zhou, A. Y., Yun, C., Lee, K., Toms, A. V., Li, Y., Dunn, G. P., Chan, E. M., Thai, T. C., et al. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.01.033 · Cited by 222
The structural basis for the sensing and binding of cyclic di-GMP by STING
Huang, Y.-H., Liu, X., Du, X., Jiang, Z., & Su, X. (2012) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2333 · Cited by 224
Interferon regulatory factors: at the crossroads of immunity, metabolism, and disease
Zhao, G., Jiang, D.-S., & Li, H. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.04.030 · Cited by 218
Hendrickx, R., Stichling, N., Koelen, J. A., Kuryk, Ł., Lipiec, A., & Greber, U. F. (2014) · Human Gene Therapy · doi:10.1089/hum.2014.001 · Cited by 221
DNA Sensing in the Innate Immune Response
Briard, B., Place, D. E., & Kanneganti, T. (2020) · Physiology · doi:10.1152/physiol.00022.2019 · Cited by 222
The interactions between cGAS-STING pathway and pathogens
Cheng, Z., Dai, T., He, X., Zhang, Z., Xie, F., Wang, S., Zhang, L., & Zhou, F. (2020) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-020-0198-7 · Cited by 216
ISG56 is a negative-feedback regulator of virus-triggered signaling and cellular antiviral response
Li, Y., Li, C., Xue, P., Zhong, B., Mao, A., Ran, Y., Chen, H., Wang, Y., Yang, F., & Shu, H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900818106 · Cited by 221
STING enhances cell death through regulation of reactive oxygen species and DNA damage
Hayman, T. J., Baro, M., MacNeil, T., Phoomak, C., Aung, T. N., Cui, W., Leach, K., Iyer, R. P., Challa, S., Sandoval-Schaefer, T., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22572-8 · Cited by 219
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
Human TBK1: A Gatekeeper of Neuroinflammation
Ahmad, L., Zhang, S.-Y., Casanova, J.-L., & Sancho-Shimizu, V. (2016) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2016.04.006 · Cited by 208
Ubiquitin in the activation and attenuation of innate antiviral immunity
Heaton, S. M., Borg, N. A., & Dixit, V. M. (2015) · The Journal of Experimental Medicine · doi:10.1084/jem.20151531 · Cited by 208
Resolving systematic errors in widely used enhancer activity assays in human cells
Muerdter, F., Boryń, Ł. M., Woodfin, A. R., Neumayr, C., Rath, M., Zabidi, M. A., Pagani, M., Haberle, V., Kazmar, T., Catarino, R. R., et al. (2018) · Nature Methods · doi:10.1038/nmeth.4534 · Cited by 208
Cytosolic DNA sensors regulating type I interferon induction
Keating, S. E., Baran, M., & Bowie, A. (2011) · Trends in Immunology · doi:10.1016/j.it.2011.08.004 · Cited by 212
ER-directed TREX1 limits cGAS activation at micronuclei
Mohr, L., Toufektchan, E., von Morgen, P., Chu, K., Kapoor, A. R., & Maciejowski, J. (2021) · Molecular Cell · doi:10.1016/j.molcel.2020.12.037 · Cited by 211
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
Hippo signalling governs cytosolic nucleic acid sensing through YAP/TAZ-mediated TBK1 blockade
Zhang, Q., Meng, F., Chen, S., Plouffe, S. W., Wu, S., Liu, S., Li, X., Zhou, R., Wang, J., Zhao, B., et al. (2017) · Nature Cell Biology · doi:10.1038/ncb3496 · Cited by 206
Tumor-targeted delivery of a STING agonist improves cancer immunotherapy
Wu, Y., Fang, Y., Qi, W., Shi, H., Tan, H., Deng, Y., Zeng, Z., Qiu, J., Chen, C., Sun, L., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2214278119 · Cited by 209
Molecular evolutionary and structural analysis of the cytosolic DNA sensor cGAS and STING
Wu, X., Wu, F.-H., Wang, X., Wang, L., Siedow, J. N., Zhang, W., & Pei, Z. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku569 · Cited by 214
Role of the cGAS–STING pathway in cancer development and oncotherapeutic approaches
Khoo, L. T., & Chen, L. (2018) · The EMBO Reports · doi:10.15252/embr.201846935 · Cited by 204
Human Cytomegalovirus Induces the Interferon Response via the DNA Sensor ZBP1
DeFilippis, V. R., Alvarado, D. M., Sali, T. M., Rothenburg, S., & Früh, K. (2009) · Journal of Virology · doi:10.1128/jvi.01748-09 · Cited by 204
Horan, K., Hansen, K., Jakobsen, M. R., Holm, C. K., Søby, S., Unterholzner, L., Thompson, M., West, J. A., Iversen, M. B., Rasmussen, S. B., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1202749 · Cited by 212
Melki, I., Rose, Y., Uggenti, C., Eyck, L. V., Frémond, M., Kitabayashi, N., Rice, G., Jenkinson, E. M., Boulai, A., Jeremiah, N., et al. (2017) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2016.10.031 · Cited by 208
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
STING-associated vasculopathy develops independently of IRF3 in mice
Warner, J. D., Irizarry-Caro, R. A., Bennion, B. G., Ai, T. L., Smith, A. M., Miner, C. A., Sakai, T., Gonugunta, V. K., Wu, J., Platt, D. J., et al. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20171351 · Cited by 210
RNF26 Temporally Regulates Virus-Triggered Type I Interferon Induction by Two Distinct Mechanisms
Qin, Y., Zhou, M., Hu, M., Hu, Y.-H., Zhang, J., Guo, L., Zhong, B., & Shu, H. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004358 · Cited by 203
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
The STING phase-separator suppresses innate immune signalling
Yu, X., Zhang, L., Shen, J., Zhai, Y., Jiang, Q., Yi, M., Deng, X., Ruan, Z., Fang, R., Chen, Z., et al. (2021) · Nature Cell Biology · doi:10.1038/s41556-021-00659-0 · Cited by 205
Corrales, L. P., & Gajewski, T. F. (2015) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-15-1362 · Cited by 206
USP13 negatively regulates antiviral responses by deubiquitinating STING
Sun, H., Zhang, Q., Jing, Y.-Y., Zhang, M., Wang, H., Cai, Z., Liuyu, T., Zhang, Z., Xiong, T.-C., Wu, Y., et al. (2017) · Nature Communications · doi:10.1038/ncomms15534 · Cited by 202
TMEM173 Drives Lethal Coagulation in Sepsis
Zhang, H., Zeng, L., Xie, M., Liu, J., Zhou, B., Wu, R., Cao, L., Kroemer, G., Wang, H., Billiar, T. R., et al. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.02.004 · Cited by 203
Post-translational regulation of inflammasomes
Yang, J., Liu, Z., & Xiao, T. S. (2016) · Cellular and Molecular Immunology · doi:10.1038/cmi.2016.29 · Cited by 211
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
Self-citationLiu, Y., Li, J., Chen, J., Li, Y., Wang, W., Du, X., Song, W., Zhang, W., Lin, L., & Yuan, Z. (2014) · Journal of Virology · doi:10.1128/jvi.02760-14 · Cited by 207
Cancer Vaccines, Adjuvants, and Delivery Systems
Paston, S. J., Brentville, V. A., Symonds, P., & Durrant, L. G. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.627932 · Cited by 200
Fu, Y.-Z., Su, S., Gao, Y.-Q., Wang, P., Huang, Z.-F., Hu, M., Luo, W.-W., Li, S., Luo, M., Wang, Y., et al. (2017) · Cell Host & Microbe · doi:10.1016/j.chom.2017.01.001 · Cited by 197
Wang, S., Xie, F., Chu, F., Zhang, Z., Yang, B., Dai, T., Gao, L., Wang, L., Ling, L., Jia, J., et al. (2017) · Nature Immunology · doi:10.1038/ni.3744 · Cited by 197
Activation of STING by targeting a pocket in the transmembrane domain
Lu, D., Shang, G., Li, J., Lu, Y. D., Bai, X., & Zhang, X. (2022) · Nature · doi:10.1038/s41586-022-04559-7 · Cited by 202
Wang, Y., Lian, Q., Yang, B., Yan, S., Zhou, H., He, L., Lin, G., Lian, Z., Jiang, Z., & Sun, B. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1005012 · Cited by 197
Species‐specific detection of the antiviral small‐molecule compound CMA by STING
Cavlar, T., Deimling, T., Ablasser, A., Hopfner, K., & Hornung, V. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.86 · Cited by 198
Zhang, J., Zhao, J., Xu, S., Li, J., He, S., Zeng, Y. A., Xie, L., Xie, N., Liu, T., Lee, K., et al. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.07.004 · Cited by 196
How Do Sensory Neurons Sense Danger Signals?
Donnelly, C. R., Ouyang, C., & Ji, R. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.07.008 · Cited by 200
NF-κB activation enhances STING signaling by altering microtubule-mediated STING trafficking
Zhang, L., Wei, X., Wang, Z., Liu, P., Hou, Y., Xu, Y., Su, H., Koci, M. D., Yin, H., & Zhang, C. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112185 · Cited by 199
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
Vila, I. K., Chamma, H., Steer, A., Saccas, M., Taffoni, C., Turtoi, E., Reinert, L. S., Hussain, S., Marines, J., Jin, L., et al. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2021.12.007 · Cited by 196
Adjuvants for peptide-based cancer vaccines
Khong, H., & Overwijk, W. W. (2016) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-016-0160-y · Cited by 190
Falahat, R., Berglund, A., Putney, R. M., Perez-Villarroel, P., Aoyama, S., Pilon-Thomas, S., Barber, G. N., & Mulé, J. J. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2013598118 · Cited by 190
Self-citationThe cGAS/STING Pathway: A Novel Target for Cancer Therapy
Gan, Y., Li, X., Han, S., Liang, Q., Ma, X., Rong, P., Wang, W., & Li, W. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.795401 · Cited by 194
Ding, Q., Gaska, J. M., Douam, F., Wei, L., Kim, D., Balev, M., Heller, B. L., & Ploß, A. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1803406115 · Cited by 200
An, X., Zhu, Y., Zheng, T., Wang, G., Zhang, M., Li, J., Ji, H., Li, S., Yang, S., Xu, D., et al. (2019) · Molecular Therapy Nucleic Acids · doi:10.1016/j.omtn.2018.11.003 · Cited by 188
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
Extrinsic Phagocyte-Dependent STING Signaling Dictates the Immunogenicity of Dying Cells
Ahn, J., Xia, T., Rabasa, A., Betancourt, D. M., & Barber, G. N. (2018) · Cancer Cell · doi:10.1016/j.ccell.2018.03.027 · Cited by 194
Self-citationHerpes Simplex Virus 1 Tegument Protein VP22 Abrogates cGAS/STING-Mediated Antiviral Innate Immunity
Huang, J. H., You, H., Su, C., Li, Y., Chen, S., & Zheng, C. (2018) · Journal of Virology · doi:10.1128/jvi.00841-18 · Cited by 188
Luke, J. J., Piha-Paul, S. A., Medina, T. M., Verschraegen, C. F., Varterasian, M. L., Brennan, A. M., Riese, R. J., Sokolovska, A., Strauss, J. F., Hava, D. L., et al. (2023) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-23-0118 · Cited by 188
Key Role of Ubc5 and Lysine-63 Polyubiquitination in Viral Activation of IRF3
Zeng, W., Xu, M., Liu, S., Sun, L., & Chen, Z. J. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.09.037 · Cited by 187
Wu, C. H., Wang, Z., Song, X., Feng, X., Abnet, C. C., He, J., Hu, N., Zuo, X.-B., Tan, W., Zhan, Q., et al. (2014) · Nature Genetics · doi:10.1038/ng.3064 · Cited by 186
Chen, S. N., Zou, P., & Nie, P. (2017) · Immunology · doi:10.1111/imm.12714 · Cited by 186
Transglutaminase Type 2 Regulates ER-Mitochondria Contact Sites by Interacting with GRP75
D’Eletto, M., Rossin, F., Occhigrossi, L., Farrace, M. G., Faccenda, D., Desai, R., Marchi, S., Refolo, G., Falasca, L., Antonioli, M., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.11.094 · Cited by 191
African swine fever virus evasion of host defences
Dixon, L. K., Islam, M., Nash, R. H., & Reis, A. L. (2019) · Virus Research · doi:10.1016/j.virusres.2019.04.002 · Cited by 190
Gozgit, J. M., Vasbinder, M. M., Abo, R., Kunii, K., Kuplast-Barr, K. G., Gui, B., Lu, A. Z., Molina, J. R., Minissale, E., Swinger, K. K., et al. (2021) · Cancer Cell · doi:10.1016/j.ccell.2021.06.018 · Cited by 191
Intrinsic Self-DNA Triggers Inflammatory Disease Dependent on STING
Ahn, J., Ruiz, P., & Barber, G. N. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1401337 · Cited by 193
Self-citationImmune Sensing Mechanisms that Discriminate Self from Altered Self and Foreign Nucleic Acids
Bartok, E., & Hartmann, G. (2020) · Immunity · doi:10.1016/j.immuni.2020.06.014 · Cited by 190
Sensing and Signaling in Antiviral Innate Immunity
O'Neill, L. A. J., & Bowie, A. (2010) · Current Biology · doi:10.1016/j.cub.2010.01.044 · Cited by 183
The AIM2-like Receptors Are Dispensable for the Interferon Response to Intracellular DNA
Gray, E. E., Winship, D., Snyder, J. M., Child, S. J., Geballe, A. P., & Stetson, D. B. (2016) · Immunity · doi:10.1016/j.immuni.2016.06.015 · Cited by 197
IL-21 and T follicular helper cells
Spolski, R. J., & Leonard, W. J. (2009) · International Immunology · doi:10.1093/intimm/dxp112 · Cited by 192
Promising Targets for Cancer Immunotherapy: TLRs, RLRs, and STING-Mediated Innate Immune Pathways
Li, K., Qu, S., Chen, X., Wu, Q., & Shi, M. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18020404 · Cited by 186
Paijo, J., Döring, M., Spanier, J., Grabski, E., Nooruzzaman, M., Schmidt, T., Witte, G., Messerle, M., Hornung, V., Kaever, V., et al. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005546 · Cited by 194
Old dogs, new trick: classic cancer therapies activate cGAS
Yum, S., Li, M., & Chen, Z. J. (2020) · Cell Research · doi:10.1038/s41422-020-0346-1 · Cited by 184
STEEP mediates STING ER exit and activation of signaling
Zhang, B., Nandakumar, R., Reinert, L. S., Huang, J., Laustsen, A., Gao, Z., Sun, C.-L., Jensen, S. B., Troldborg, A., Assil, S., et al. (2020) · Nature Immunology · doi:10.1038/s41590-020-0730-5 · Cited by 184
Lei, C., Zhong, B., Zhang, Y., Zhang, J., Wang, S., & Shu, H. (2010) · Immunity · doi:10.1016/j.immuni.2010.11.021 · Cited by 180
Sze, A., Belgnaoui, S. M., Olagnier, D. P., Lin, R., Hiscott, J. B., & van Grevenynghe, J. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.09.009 · Cited by 188
Hepatitis C virus NS4B blocks the interaction of STING and TBK1 to evade host innate immunity
Ding, Q., Cao, X., Lu, J. L., Huang, B. S., Liu, Y.-J., Kato, N., Shu, H., & Zhong, J. (2013) · Journal of Hepatology · doi:10.1016/j.jhep.2013.03.019 · Cited by 187
Berger, G., Knelson, E. H., Jimenez-Macias, J. L., Nowicki, M. O., Han, S., Panagioti, E., Lizotte, P. H., Adu-Berchie, K., Stafford, A., Dimitrakakis, N., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2111003119 · Cited by 179
Fullam, A., & Schröder, M. (2013) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2013.03.012 · Cited by 182
Nuclear interferon-inducible protein 16 promotes silencing of herpesviral and transfected DNA
Orzalli, M. H., Conwell, S. E., Berrios, C. J., DeCaprio, J. A., & Knipe, D. M. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1316194110 · Cited by 184
Therapeutically Active RIG-I Agonist Induces Immunogenic Tumor Cell Killing in Breast Cancers
Elion, D. L., Jacobson, M. E., Hicks, D. J., Rahman, B., Sanchez, V. M., Ericsson, P. I. G., Fedorova, O., Pyle, A. M., Wilson, J. T., & Cook, R. S. (2018) · Cancer Research · doi:10.1158/0008-5472.can-18-0730 · Cited by 178
Delivery of STING agonists for adjuvanting subunit vaccines
Herck, S. V., Feng, B., & Tang, L. (2021) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2021.114020 · Cited by 182
Cai, H., Yan, L., Liu, N., Xu, M. M., & Cai, H. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.109790 · Cited by 179
Mathur, V., Burai, R., Vest, R. T., Bonanno, L. N., Lehallier, B., Zardeneta, M. E., Mistry, K. N., Do, D., Marsh, S. E., Abud, E. M., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.11.032 · Cited by 175
The cGAS-STING Pathway for DNA Sensing
Xiao, T. S., & Fitzgerald, K. A. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.07.004 · Cited by 177
Dubensky, T. W., Kanne, D. B., & Leong, M. L. L. (2013) · Therapeutic Advances in Vaccines · doi:10.1177/2051013613501988 · Cited by 176
Evasion of host antiviral innate immunity by HSV-1, an update
Su, C., Zhan, G., & Zheng, C. (2016) · Virology Journal · doi:10.1186/s12985-016-0495-5 · Cited by 175
Su, C., & Zheng, C. (2017) · Journal of Virology · doi:10.1128/jvi.02414-16 · Cited by 175
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
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