The DOI matches its Crossref record; 39 of the 39 references it cites were found in a registry or an index.
IL-33, the IL-1-like cytokine ligand for ST2 receptor, is a chromatin-associated nuclear factor in vivo
Open accessAbstract
Recent studies indicate that IL-1α functions intracellularly in pathways independent of its cell surface receptors by translocating to the nucleus and regulating transcription. Similarly, the chromatin-associated protein HMGB1 acts as both a nuclear factor and a secreted proinflammatory cytokine. Here, we show that IL-33, an IL-1-like cytokine that signals via the IL-1 receptor-related protein ST2 and induces T helper type 2-associated cytokines, is an endothelium-derived, chromatin-associated nuclear factor with transcriptional repressor properties. We found that IL-33 is identical to NF-HEV, a nuclear factor preferentially expressed in high endothelial venules (HEV), that we previously characterized. Accordingly, in situ hybridization demonstrated that endothelial cells constitute a major source of IL-33 mRNA in chronically inflamed tissues from patients with rheumatoid arthritis and Crohn's disease. Immunostaining with three distinct antisera, directed against the N-terminal part and IL-1-like C-terminal domain, revealed that IL-33 is a heterochromatin-associated nuclear factor in HEV endothelial cells in vivo . Association of IL-33 with heterochromatin was also observed in human and mouse cells under living conditions. In addition, colocalization of IL-33 with mitotic chromatin was noted. Nuclear localization, heterochromatin-association, and targeting to mitotic chromosomes were all found to be mediated by an evolutionarily conserved homeodomain-like helix–turn–helix motif within the IL-33 N-terminal part. Finally, IL-33 was found to possess transcriptional repressor properties, associated with the homeodomain-like helix–turn–helix motif. Together, these data suggest that, similarly to IL1α and HMGB1, IL-33 is a dual function protein that may function as both a proinflammatory cytokine and an intracellular nuclear factor with transcriptional regulatory properties.
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?
In the citing paper
“IL-33 is highly expressed within endothelial cells in the synovium of patients with rheumatoid arthritis87, and IL-33-deficient mice have reduced neutrophil migration in an experimental model of rheumatoid arthritis88, but the actual role of this cytokine in the pathogenesis of rheumatoid arthritis or other sterile inflammatory diseases remains to be determined.”
From Sterile inflammation: sensing and reacting to damage (2010) · cites this paper as [87]
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
Biologic basis for interleukin-1 in disease.
Dinarello, C. (1996) · Blood · doi:10.1182/blood.v87.6.2095.bloodjournal8762095 · Cited by 4,344
Release of chromatin protein HMGB1 by necrotic cells triggers inflammation
Scaffidi, P., Misteli, T., & Bianchi, M. E. (2002) · Nature · doi:10.1038/nature00858 · Cited by 4,221
Schmitz, J., Owyang, A. M., Oldham, E. R., Song, Y., Murphy, E., McClanahan, T. K., Zurawski, G., Moshrefi, M., Qin, J., Li, X., et al. (2005) · Immunity · doi:10.1016/j.immuni.2005.09.015 · Cited by 3,773
HMG-1 as a Late Mediator of Endotoxin Lethality in Mice
Wang, H., Bloom, O., Zhang, M., Vishnubhakat, J. M., Ombrellino, M., Che, J., Frazier, A., Yang, H., Ivanova, S., Borovikova, L. V., et al. (1999) · Science · doi:10.1126/science.285.5425.248 · Cited by 3,386
Yang, Y., Li, S., Yang, Q., Shi, Y., Zheng, M., Liu, Y., Chen, F., Song, G., Xu, H., Wan, T., et al. (2014) · Cellular Physiology and Biochemistry · doi:10.1159/000358696 · Cited by 3,263
High-mobility group box 1 protein (HMGB1): nuclear weapon in the immune arsenal
Lotze, M. T., & Tracey, K. J. (2005) · Nature reviews. Immunology · doi:10.1038/nri1594 · Cited by 2,490
Monocytic cells hyperacetylate chromatin protein HMGB1 to redirect it towards secretion
Bonaldi, T., Talamo, F., Scaffidi, P., Ferrera, D., Porto, A., Bachi, A., Rubartelli, A., Agresti, A., & Bianchi, M. E. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg516 · Cited by 1,252
Association of transcriptionally silent genes with Ikaros complexes at centromeric heterochromatin.
Brown, K., Guest, S. S., Smale, S., Hahm, K., Merkenschlager, M., & Fisher, A. (1997) · Cell · doi:10.1016/s0092-8674(00)80472-9 · Cited by 824
HMG1 and 2, and related ‘architectural’ DNA-binding proteins
Thomas, J. O., & TRAVERS, A. A. (2001) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(01)01801-1 · Cited by 619
Ikaros DNA-Binding Proteins Direct Formation of Chromatin Remodeling Complexes in Lymphocytes
Kim, J., Sif, S., Jones, B., Jackson, A., Koipally, J., Heller, E., Winandy, S., Viel, A., Sawyer, A., Ikeda, T., et al. (1999) · Immunity · doi:10.1016/s1074-7613(00)80034-5 · Cited by 587
Research works printed but not linked: 1
- CA Dinarello Eur Cytokine Netw 11, 483–486 (2000).
Cited by
Sorted by citations
Items 401–500 of 965
Sex differences in the molecular signature of the developing mouse hippocampus
Bundy, J. L., Vied, C., & Nowakowski, R. S. (2017) · BMC Genomics · doi:10.1186/s12864-017-3608-7 · Cited by 54
Dichotomous function of IL-33 in health and disease: From biology to clinical implications
Braun, H., Afonina, I. S., Mueller, C., & Beyaert, R. (2018) · Biochemical Pharmacology · doi:10.1016/j.bcp.2018.01.010 · Cited by 50
Basal epithelial stem cells cross an alarmin checkpoint for postviral lung disease
Wu, K., Kamimoto, K., Zhang, Y., Yang, K., Keeler, S. P., Gerovac, B. J., Agapov, E. V., Austin, S. R., Yantis, J., Gissy, K. A., et al. (2021) · Journal of Clinical Investigation · doi:10.1172/jci149336 · Cited by 50
Unconventional Pathways of Secretion Contribute to Inflammation
Daniels, M. J. D., & Brough, D. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18010102 · Cited by 50
IL-33 released by alum is responsible for early cytokine production and has adjuvant properties
Rose, W., Okragly, A. J., Patel, C. N., & Benschop, R. J. (2015) · Scientific Reports · doi:10.1038/srep13146 · Cited by 51
Paracrine IL-33 Stimulation Enhances Lipopolysaccharide-Mediated Macrophage Activation
Ohno, T., Oboki, K., Morita, H., Kajiwara, N., Arae, K., Tanaka, S., Ikeda, M., Iikura, M., Akiyama, T., Inoue, J., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018404 · Cited by 49
Bianchetti, L., Marini, M. A., Isgrò, M., Bellini, A., Schmidt, M., & Mattoli, S. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.08.047 · Cited by 49
Patel, N. N., Kohanski, M. A., Maina, I. W., Workman, A. D., Herbert, D. R., & Cohen, N. A. (2018) · International Forum of Allergy & Rhinology · doi:10.1002/alr.22206 · Cited by 48
IL-36 family cytokines in protective versus destructive inflammation
Han, Y., Huard, A., Mora, J., da Silva, P., Brüne, B., & Weigert, A. (2020) · Cellular Signalling · doi:10.1016/j.cellsig.2020.109773 · Cited by 50
The IL-1 Family and Its Role in Atherosclerosis
González, L., Rivera, K., Andía, M. E., & Martı́nez-Rodrı́guez, G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010017 · Cited by 51
Murine Mast Cells Secrete and Respond to Interleukin-33
Tung, H.-Y., Plunkett, B., Huang, S.-K., & Zhou, Y. (2013) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2012.0066 · Cited by 48
Nuclear retention of IL‐1α by necrotic cells: A mechanism to dampen sterile inflammation
Luheshi, N., McColl, B. W., & Brough, D. (2009) · European Journal of Immunology · doi:10.1002/eji.200939712 · Cited by 48
Kang, H., Yang, K., Xiao, L., Guo, L., Guo, C.-J., Yan, Y., Jin, Q., Wang, F., Ryffel, B., Li, C., et al. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01312 · Cited by 49
The Dynamics and Mechanisms of Interleukin‐1α and β Nuclear Import
Luheshi, N., Rothwell, N. J., & Brough, D. (2008) · Traffic · doi:10.1111/j.1600-0854.2008.00840.x · Cited by 48
Sawada, J., Hiraoka, N., Qi, R., Jiang, L., Fournier-Goss, A. E., Yoshida, M., Kawashima, H., & Komatsu, M. (2022) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-21-0369 · Cited by 47
Dual Immune Regulatory Roles of Interleukin-33 in Pathological Conditions
Guo, H., Bossila, E. A., Ma, X., Zhao, C., & Zhao, Y. X. (2022) · Cells · doi:10.3390/cells11203237 · Cited by 54
Koyasu, S., Moro, K., Tanabe, M., & Takeuchi, T. (2010) · Advances in immunology · doi:10.1016/b978-0-12-380995-7.00002-1 · Cited by 50
Taniguchi, K., Yamamoto, S., Hitomi, E., Inada, Y., Suyama, Y., Sugioka, T., & Hamasaki, Y. (2013) · PubMed · Cited by 47
Chen, S., Chen, B., Wen, Z., Huang, Z. W., & Ye, L. (2017) · Oncotarget · doi:10.18632/oncotarget.16299 · Cited by 47
Zhuang, X., Zhan, B., Jia, Y., Li, C., Wu, N., Zhao, M., Chen, N., Guo, Y., Du, Y., Zhang, Y., et al. (2022) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2022.02.019 · Cited by 48
Signaling and functions of interleukin-33 in immune regulation and diseases
Yi, X.-M., Lian, H., & Li, S. (2022) · Cell Insight · doi:10.1016/j.cellin.2022.100042 · Cited by 46
Wang, X., Hallen, N. R., Lee, M., Samuchiwal, S. K., Ye, Q., Buchheit, K. M., Maxfield, A. Z., Roditi, R. E., Bergmark, R. W., Bhattacharyya, N., et al. (2022) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2023.01.030 · Cited by 46
Lee, E.-J., So, M. W., Hong, S., Kim, Y., Yoo, B., & Lee, C. (2015) · Cytokine · doi:10.1016/j.cyto.2015.10.005 · Cited by 46
Nomura, K., Kojima, T., Fuchimoto, J., Obata, K., Keira, T., Himi, T., & Sawada, N. (2012) · The Laryngoscope · doi:10.1002/lary.23261 · Cited by 46
IL-33-ST2 Axis in Liver Disease: Progression and Challenge
Sun, Z., Chang, B., Gao, M., Zhang, J., & Zou, Z. (2017) · Mediators of Inflammation · doi:10.1155/2017/5314213 · Cited by 47
IL-33/ST2 Pathway as a Rational Therapeutic Target for CNS Diseases
Du, L., Wang, Y., Hua, G., & Mi, W. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.11.028 · Cited by 46
Current perspectives on the interleukin‐1 family as targets for inflammatory disease
Hernandez-Santana, Y., Giannoudaki, E., León, G., Lucitt, M. B., & Walsh, P. T. (2019) · European Journal of Immunology · doi:10.1002/eji.201848056 · Cited by 47
Qi, F., Wang, D., Liu, J., Zeng, S., Xu, L., Hu, H., & Liu, B. (2015) · International Immunopharmacology · doi:10.1016/j.intimp.2015.10.022 · Cited by 46
Millar, N. L., O’Donnell, C., McInnes, I. B., & Brint, E. K. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.08.007 · Cited by 45
Mishra, P. K., Palma, M., Buechel, B., Moore, J., Davra, V., Chu, N., Millman, A., Hallab, N. J., Kanneganti, T., Birge, R. B., et al. (2019) · Nature Materials · doi:10.1038/s41563-018-0271-6 · Cited by 44
Aparicio‐Domingo, P., Cannelle, H., Buechler, M. B., Nguyen, S., Kallert, S. M., Favre, S., Alouche, N., Papazian, N., Ludewig, B., Cupedo, T., et al. (2020) · European Journal of Immunology · doi:10.1002/eji.201948413 · Cited by 44
IL-1/IL-1R Signaling in Head and Neck Cancer
Niklander, S. E., Murdoch, C., & Hunter, K. D. (2021) · Frontiers in Oral Health · doi:10.3389/froh.2021.722676 · Cited by 43
IL-33–Induced Hematopoietic Stem and Progenitor Cell Mobilization Depends upon CCR2
Kim, J., Kim, W., Le, H. T., Moon, U. J., Tran, V. G., Kim, H. J., Jung, S., Nguyen, Q.-T., Kim, B.-S., Jun, J., et al. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1400176 · Cited by 45
The multi‐faceted role of allergen exposure to the local airway mucosa
Golebski, K., Röschmann, K., Toppila-Salmi, S. K., Hammad, H., Lambrecht, B. N., Renkonen, R., Fokkens, W. J., & van Drunen, C. M. (2012) · Allergy · doi:10.1111/all.12080 · Cited by 46
Group 2 innate lymphoid cells: new players in human allergic diseases.
Doherty, T. A., & Broide, D. H. (2015) · PubMed · Cited by 44
The role of the IL-33/ST2 axis in autoimmune disorders: Friend or foe?
Liu, X., Xiao, Y., Pan, Y., Li, H., Zheng, S. G., & Su, W. (2019) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2019.04.004 · Cited by 44
Skin Immunity and Tolerance: Focus on Epidermal Keratinocytes Expressing HLA-G
Mestrallet, G., Rouas‐Freiss, N., LeMaoult, J., Fortunel, N. O., & Martin, M. T. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.772516 · Cited by 43
A role for interleukin-33 in TH2-polarized intestinal inflammation?
Seidelin, J. B., Rogler, G., & Nielsen, O. H. (2011) · Mucosal Immunology · doi:10.1038/mi.2011.22 · Cited by 43
Osteoprotective Effects of IL-33/ST2 Link to Osteoclast Apoptosis
Lima, I. L. D. A., Macari, S., Madeira, M. F. M., Rodrigues, L. F. D., Colavite, P. M., Garlet, G. P., Soriani, F. M., Teixeira, M. M., Fukada, S. Y., & Silva, T. A. (2015) · American Journal Of Pathology · doi:10.1016/j.ajpath.2015.08.013 · Cited by 43
IL33 and Mast Cells—The Key Regulators of Immune Responses in Gastrointestinal Cancers?
Eissmann, M. F., Büchert, M., & Ernst, M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01389 · Cited by 45
Wu, M., Wang, S., Xie, Y., Chen, Z., Guo, Q., Yuan, W., Guan, C., Xu, C., Huang, Y., Wang, J., et al. (2020) · Journal of Cellular Physiology · doi:10.1002/jcp.30158 · Cited by 43
Role of the IL-33/ST2L axis in colorectal cancer progression
Akimoto, M., & Takenaga, K. (2018) · Cellular Immunology · doi:10.1016/j.cellimm.2017.12.014 · Cited by 42
Critical Roles of IL-33/ST2 Pathway in Neurological Disorders
Isnadi, M. F. A. R., Chin, V. K., Majid, R. A., Lee, T. Y., Abdullah, M. A., Bello, R. O., Ibraheem, Z. O., & Basir, R. (2018) · Mediators of Inflammation · doi:10.1155/2018/5346413 · Cited by 42
Interleukin-33 and ST2 Signaling in Tumor Microenvironment
Hong, J., Kim, S., & Lin, P. C. (2018) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2018.0044 · Cited by 43
Caspase 1 deficiency reduces inflammation-induced brain transcription
Mastronardi, C. A., Whelan, F., Yildiz, O. A., Hannestad, J. O., Elashoff, D. A., McCann, S. M., Licinio, J., & Wong, M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701366104 · Cited by 42
Microglia and Brain Macrophages as Drivers of Glioma Progression
Zheng, Y., & Graeber, M. B. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232415612 · Cited by 40
Wang, Z., Pan, B., Qiu, J., Zhang, X., Ke, X., Shen, S., Wu, X., Yao, Y., & Tang, N. (2023) · Science Signaling · doi:10.1126/scisignal.abq3362 · Cited by 42
Serum amyloid A induces interleukin‐33 expression through an IRF7‐dependent pathway
Sun, L., Zhu, Z., Cheng, N., Yan, Q., & Ye, R. D. (2014) · European Journal of Immunology · doi:10.1002/eji.201344310 · Cited by 41
Research progress on interleukin-33 and its roles in the central nervous system
Han, P., Mi, W., & Wang, Y.-Q. (2011) · Neuroscience Bulletin · doi:10.1007/s12264-011-1025-5 · Cited by 41
Zhu, J., Wang, Y., Yang, F., Sang, L.-X., Zhai, J., Li, S., Li, Y., Wang, D., Lu, C., & Sun, X. (2015) · International Immunopharmacology · doi:10.1016/j.intimp.2015.08.032 · Cited by 41
IFN-γ Directly Controls IL-33 Protein Level through a STAT1- and LMP2-dependent Mechanism
Kopach, P., Lockatell, V., Pickering, E. M., Haskell, R. E., Anderson, R. D., Hasday, J. D., Todd, N. W., Luzina, I. G., & Atamas, S. P. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.534396 · Cited by 41
Disease severity in K/BxN serum transfer-induced arthritis is not affected by IL-33 deficiency
Martin, P., Talabot‐Ayer, D., Seemayer, C. A., Vigne, S., Lamacchia, C., Rodriguez, E., Finckh, A., Smith, D. E., Gabay, C., & Palmer, G. (2013) · Arthritis Research & Therapy · doi:10.1186/ar4143 · Cited by 43
Le, H. T., Kim, W., Kim, J., Cho, H. R., & Kwon, B. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00104 · Cited by 42
Noncanonical intracrine action
Ré, R. N., & Cook, J. L. (2011) · Journal of the American Society of Hypertension · doi:10.1016/j.jash.2011.07.001 · Cited by 41
The Deubiquitinase USP17 Regulates the Stability and Nuclear Function of IL-33
Ni, Y., Tao, L., Chen, C., Song, H., Li, Z., Gao, Y., Nie, J., Piccioni, M., Shi, G., & Li, B. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms161126063 · Cited by 41
Alarmins and central nervous system inflammation in HIV ‐associated neurological disorders
Gougeon, M. (2016) · Journal of Internal Medicine · doi:10.1111/joim.12570 · Cited by 41
Yap, G. S., & Gause, W. C. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02135 · Cited by 43
NOD1 is required forHelicobacter pyloriinduction of IL-33 responses in gastric epithelial cells
Tran, L. S., Tran, D., Paoli, A. D., D’Costa, K., Creed, S. J., Ng, G. Z., Le, L., SUTTON, P. R. N., Silke, J., Nachbur, U., et al. (2018) · Cellular Microbiology · doi:10.1111/cmi.12826 · Cited by 42
Lin, C. Y., Pfluger, C. M., Henderson, R. D., & McCombe, P. (2012) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2012.05.001 · Cited by 41
Shen, J., Shang, Q., Wong, C. K., Li, E. K., Wang, S., Li, R., Lee, K.-L., Leung, Y.-Y., Ying, K.-Y., Yim, C.-W., et al. (2015) · Seminars in Arthritis and Rheumatism · doi:10.1016/j.semarthrit.2015.02.001 · Cited by 40
Kageyama, Y., Torikai, E., Tsujimura, K., & Kobayashi, M. (2011) · Modern Rheumatology · doi:10.1007/s10165-011-0480-1 · Cited by 40
Developmental expression of IL-33 in the mouse brain
Wicher, G., Husic, E., Nilsson, G. P., & Forsberg‐Nilsson, K. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2013.09.046 · Cited by 40
Similarities and differences in inflammatory mechanisms of asthma and COPD
Barnes, P. J. (2011) · Breathe · doi:10.1183/20734735.026410 · Cited by 42
The Janus Face of IL-33 Signaling in Tumor Development and Immune Escape
Choi, M.-R., Sosman, J. A., & Zhang, B. (2021) · Cancers · doi:10.3390/cancers13133281 · Cited by 40
Sokołowska, M., Głobińska, A., & Akdiş, C. A. (2017) · Wiley-VCH eBooks · doi:10.1002/9783527692156.ch38 · Cited by 40
Interleukin-33 mediates formalin-induced inflammatory pain in mice
Han, P., Zhao, J., Liu, S.-B., Yang, C.-J., Wang, Y., Wu, G. C., Xu, D., & Mi, W. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.03.019 · Cited by 40
Koyasu, S., & Moro, K. (2011) · Current Opinion in Allergy and Clinical Immunology · doi:10.1097/aci.0b013e3283448808 · Cited by 39
Interleukin‐33 could play an important role in the pathogenesis of periodontitis
Köseoğlu, S., Hatipoğlu, M., Sağlam, M., Enhoş, Ş., & Esen, H. H. (2014) · Journal of Periodontal Research · doi:10.1111/jre.12235 · Cited by 39
Hoogerwerf, J. J., Leendertse, M., Wieland, C. W., de Vos, A. F., de Boer, J. D., Florquin, S., & van der Poll, T. (2010) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201006-0934oc · Cited by 41
Red Blood Cells Store and Release Interleukin-33
Wei, J., Zhao, J., Schrott, V. M., Zhang, Y., Gladwin, M. T., Bullock, G. C., & Zhao, Y. (2015) · Journal of Investigative Medicine · doi:10.1097/jim.0000000000000213 · Cited by 41
Pathophysiologic role of Interleukin-33/ST2 in Sjögren's syndrome
Soyfoo, M. S., & Nicaise, C. (2021) · Autoimmunity Reviews · doi:10.1016/j.autrev.2021.102756 · Cited by 39
Dong, Y., Zhong, J., & Dong, L. (2021) · Frontiers in Medicine · doi:10.3389/fmed.2021.739489 · Cited by 43
IL-33: A central cytokine in helminth infections
McSorley, H. J., & Smyth, D. J. (2021) · Seminars in Immunology · doi:10.1016/j.smim.2021.101532 · Cited by 44
ST2 Protein in Heart Disease: From Discovery to Mechanisms and Prognostic Value
Weinberg, E. O. (2009) · Biomarkers in Medicine · doi:10.2217/bmm.09.56 · Cited by 41
Biomarkers for cardiovascular disease: challenges and future directions
May, A., & Wang, T. J. (2008) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2008.04.003 · Cited by 39
Interleukin-33 in human gliomas: Expression and prognostic significance
Gramatzki, D., Frei, K., Cathomas, G., Moch, H., Weller, M., & Mertz, K. D. (2016) · Oncology Letters · doi:10.3892/ol.2016.4626 · Cited by 39
Hai, S., Li, X., Xie, E., Wu, W., Gao, Q., Yu, B., Hu, J., Xu, F., Zheng, X., Zhang, B., et al. (2024) · Hepatology · doi:10.1097/hep.0000000000000985 · Cited by 38
IL-33 and kidney disease (Review)
Yang, F., ZHU, P., Duan, L., Yang, L., & Wang, J. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.4516 · Cited by 37
Li, C.-W., Chen, K., Kang, H., Yan, Y.-F., Liu, K., Guo, C.-J., Qi, J., Yang, K., Wang, F., Guo, L., et al. (2017) · Cell Death and Disease · doi:10.1038/cddis.2017.534 · Cited by 35
IL-33 contributes to disease severity in Psoriasis-like models of mouse
Duan, Y., Dong, Y.-H., Hu, H., Wang, Q., Guo, S. J., Fu, D., Song, X., Kalvakolanu, D. V., & Tian, Z. (2019) · Cytokine · doi:10.1016/j.cyto.2019.02.019 · Cited by 38
Canè, L., Poto, R., Palestra, F., Pirozzi, M., Parashuraman, S., Iacobucci, I., Ferrara, A. L., Rocca, A. L., Mercadante, E., Pucci, P., et al. (2024) · European Journal of Internal Medicine · doi:10.1016/j.ejim.2024.02.020 · Cited by 39
Lai, Y.-T., Qiu, R.-R., Zhou, J., Ren, L., Qu, Y., & Zhang, G. (2025) · Inflammation · doi:10.1007/s10753-024-02233-w · Cited by 37
Baumann, R., Rabaszowski, M., Stenin, I., Tilgner, L., Gärtner-Akerboom, M., Scheckenbach, K., Wiltfang, J., Chaker, A. M., Schipper, J., & Wagenmann, M. (2013) · Clinical & Experimental Allergy · doi:10.1111/cea.12148 · Cited by 37
Targeting ST2L Potentiates CpG-Mediated Therapeutic Effects in a Chronic Fungal Asthma Model
Ramaprakash, H., Shibata, T., Duffy, K. E., Ismailoglu, U. B., Bredernitz, R. M., Serezani, A. P. M., Coelho, A. L., Das, A., Fursov, N., Chupp, G. L., et al. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2011.03.032 · Cited by 37
Tristetraprolin inhibits gastric cancer progression through suppression of IL-33
Deng, K., Wang, H., Shan, T., Chen, Y., Zhou, H. Y., Zhao, Q., & Xia, J. (2016) · Scientific Reports · doi:10.1038/srep24505 · Cited by 38
Nuclear Alarmin Cytokines in Inflammation
Jiang, L., Shao, Y., Tian, Y., Ouyang, C., & Wang, X. (2020) · Journal of Immunology Research · doi:10.1155/2020/7206451 · Cited by 38
Roussel, L., Farias, R., & Rousseau, S. (2012) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2012.10.019 · Cited by 40
Self-citationKim, D.-J., Baek, S.-Y., Park, M.-K., Park, K.-S., Lee, J. H., Park, S., Kim, H., & Kwok, S. (2013) · Journal of Korean Medical Science · doi:10.3346/jkms.2013.28.8.1145 · Cited by 37
Modulation of IL-33/ST2 signaling as a potential new therapeutic target for cardiovascular diseases
Thanikachalam, P. V., Ramamurthy, S., Mallapu, P., Varma, S. R., Jayaraj, K. N., Abourehab, M. A. S., & Kesharwani, P. (2023) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2023.06.003 · Cited by 38
Xiao, A.-W., He, J., Wang, Q., Luo, Y., Sun, Y., Zhou, Y., Yang, G., Lucassen, P. J., & Dai, J. (2011) · Neuroscience Bulletin · doi:10.1007/s12264-011-1736-7 · Cited by 36
Cancer stem cells and their niche in the progression of squamous cell carcinoma
Oshimori, N. (2020) · Cancer Science · doi:10.1111/cas.14639 · Cited by 38
The Paradigm of the Inflammatory Radicular Cyst: Biological Aspects to be Considered
Osorio, N. R. R., Caviedes‐Bucheli, J., Mosquera-Guevara, L., Adames-Martinez, J. S., Gomez-Pinto, D., Jimenez-Jimenez, K., Maz, H. H. A., & Bornacelly-Mendoza, S. (2022) · European Endodontic Journal · doi:10.14744/eej.2022.26918 · Cited by 35
Alarmin’ Immunologists: IL-33 as a Putative Target for Modulating T Cell-Dependent Responses
Gajardo, T., Morales, R. A., Pérez, F., Terraza, C., Yáñez, L., Campos‐Mora, M., & Pino‐Lagos, K. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00232 · Cited by 35
Mine, Y., Makihira, S., Yamaguchi, Y., Tanaka, H., & Nikawa, H. (2014) · Cell Biology International · doi:10.1002/cbin.10249 · Cited by 36
Epithelial-derived nuclear IL-33 aggravates inflammation in the pathogenesis of reflux esophagitis
Shan, J., Oshima, T., Muto, T., Yasuda, K., Fukui, H., Watari, J., Nakanishi, K., & Miwa, H. (2014) · Journal of Gastroenterology · doi:10.1007/s00535-014-0988-1 · Cited by 36
The Evolutionary Role of the IL-33/ST2 System in Host Immune Defence
Sattler, S., Smits, H. H., Xu, D., & Huang, F. (2013) · Archivum Immunologiae et Therapiae Experimentalis · doi:10.1007/s00005-012-0208-8 · Cited by 38
Schröder, P. C., Casaca, V. I., Illi, S., Schieck, M., Michel, S., Böck, A., Roduit, C., Frei, R., Lluis, A., Genuneit, J., et al. (2016) · Pediatric Allergy and Immunology · doi:10.1111/pai.12597 · Cited by 35
Multifaceted roles of IL-38 in inflammation and cancer
Díaz-Barreiro, A., Huard, A., & Palmer, G. (2022) · Cytokine · doi:10.1016/j.cyto.2022.155808 · Cited by 36
Novel Splice Variants of IL-33: Differential Expression in Normal and Transformed Cells
Tsuda, H., Komine, M., Karakawa, M., Etoh, T., Tominaga, S., & Ohtsuki, M. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2012.180 · Cited by 36
Ahmed, A., Hollan, I., Curran, S. A., Kitson, S. M., Riggio, M. P., Mikkelsen, K., Almdahl, S. M., Aukrust, P., McInnes, I. B., & Goodyear, C. S. (2016) · Arthritis & Rheumatology · doi:10.1002/art.39574 · Cited by 35
Metadata
- Authors
- Carriere, V., Roussel, L., Ortega, N., Lacorre, D.-A., Americh, L., Aguilar, L., Bouche, G., & Girard, J.-P.
- Affiliations
- *Laboratoire de Biologie Vasculaire, Equipe Labellisée “La Ligue 2006,” Institut de Pharmacologie et de Biologie Structurale, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5089, 205 Route de Narbonne, 31077 Toulouse, France; and
- Centre National de la Recherche Scientifique (FR)
- Endocube, Prologue Biotech, BP700, Rue Pierre et Marie Curie, 31319 Labège Cedex, France
- Corresponding author
- Girard, Jean-Philippe
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2007-01-02
- Volume
- 104
- Issue
- 1
- Pages
- 282-287
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC1765450
- OpenAlex
- W2093396768
- Cited by
- 966
- References
- 38
- Citations by year
- 2026: 20 · 2025: 29 · 2024: 30 · 2023: 49 · 2022: 50 · 2021: 51 · 2020: 47 · 2019: 51 · 2018: 58 · 2017: 55 · 2016: 64 · 2015: 70 · 2014: 52 · 2013: 56 · 2012: 72
- FWCI
- 12.14
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Association pour la Recherche sur le Cancer
- Drug Applied Research Center, Tabriz University of Medical Sciences
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › IL-33, ST2, and ILC Pathways
- Life Sciences › Immunology and Microbiology › Immunology › Cytokine Signaling Pathways and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- IL-33, ST2 receptor, heterochromatin, nuclear factors, transcriptional repressor, endothelial cells, high endothelial venules, rheumatoid arthritis, Crohn's disease, chronic inflammation, HMGB1
- MeSH terms
- Interleukin-33, Interleukin-1 Receptor-Like 1 Protein, Animals, Arthritis, Rheumatoid, Crohn Disease, HeLa Cells, Heterochromatin, Humans, Interleukins, Membrane Proteins, Mitosis, Nuclear Proteins, Receptors, Cell Surface, Repressor Proteins, RNA, Messenger, 3T3 Cells, Conserved Sequence, Receptors, Interleukin, Nuclear Localization Signals, Amino Acid Motifs, Endothelial Cells, 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