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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.
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“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]
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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
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Wang, H., Hu, Y., Li, Z., Wu, E., Yuan, Q., Niu, X., Liu, J., Cai, H., Qin, M., Xu, J., et al. (2025) · Andrology · doi:10.1111/andr.70078 · Cited by 4
Diagnostic accuracy of interleukin-33 for tuberculous pleural effusion
Shi, X., Yi, F., Qiao, X., Pei, X., & Dong, S. (2021) · Medicine · doi:10.1097/md.0000000000026755 · Cited by 4
Orchestrated regulation of immune inflammation with cell therapy in pediatric acute liver injury
Duan, M., Liu, X., Yang, Y., Zhang, Y., Wu, R., Lv, Y., & Lei, H. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1194588 · Cited by 4
El-Deen, E. M. N., Hassan, W. A., Behiry, E. G., & El-monem, A. E.-H. A. (2020) · The Egyptian Rheumatologist · doi:10.1016/j.ejr.2020.02.005 · Cited by 4
Knowledge mapping of interleukin-33: a bibliometric study.
Sun, J., Xia, Y., Zhang, D., Yu, Z., Ning, Y., & Tan, Z. (2023) · PubMed Central · Cited by 4
Panavas, T., Lu, J. Y., Liu, X., Winkis, A., Powers, G. D., Naso, M. F., & Amegadzie, B. Y. (2011) · Protein Expression and Purification · doi:10.1016/j.pep.2011.05.011 · Cited by 4
Impact of Cytokines in Mast cells Allergic Inflammation
Conti, P. (2013) · Cited by 4
Development of an interleukin (IL)-33 sandwich ELISA kit specific for mature IL-33
Kim, E., Kwak, A., Jhun, H., Lee, S., Jo, S., Lee, J., Kang, T., Her, E., Bae, S., Lee, Y. M., et al. (2016) · Journal of Immunoassay and Immunochemistry · doi:10.1080/15321819.2016.1179645 · Cited by 4
Dinarello, C. A., & Netea, M. G. (2013) · Springer eBooks · doi:10.1007/978-4-431-54442-5_1 · Cited by 4
Mechanisms in COPD compared with asthma
Barnes, P. J. (2008) · Breathe · doi:10.1183/18106838/breathe.5.2.134 · Cited by 4
Shi, P., Sun, P., Lou, C., Fang, J., Zhang, L., Xie, B., & Zhang, C. (2024) · Journal of Surgical Research · doi:10.1016/j.jss.2024.11.017 · Cited by 3
Cytokine, cytokine storm and their role in fatalities of COVID-19
Roy, S. C. (2021) · Journal of Infectious Diseases and Immunity · doi:10.5897/jidi2021.0216 · Cited by 3
IL-33 deficiency suppresses alveolar bone loss in a ligature-induced periodontitis model
Aida, N., Takeda, K., Nakae, S., Saito, H., Okumura, K., Azuma, T., & Ohno, T. (2023) · Biomedical Research · doi:10.2220/biomedres.44.9 · Cited by 5
Shilovskiy, I. P., Драгановна, Т. Е., Михайловна, К. М., Pasikhov, G. B., Tahanovich, A. D., Kadushkin, A. G., Гудима, Г. О., & Khaitov, M. R. (2024) · Immunologiya · doi:10.33029/1816-2134-2024-45-2-245-255 · Cited by 3
Liu, T., & Li, X. (2025) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.70460 · Cited by 3
Unlocking IL-33: New Insights into Tumor Immunity
Kang, B. H., & Lee, H. K. (2025) · Immune Network · doi:10.4110/in.2025.25.e36 · Cited by 3
Benedetto, C. D., Khan, T., Serrano-Saenz, S., Rodriguez-Lemus, A., Klomsiri, C., Beutel, T.-M., Thach, A., Walczak, H., & Betancur, P. A. (2023) · Cancers · doi:10.3390/cancers15030967 · Cited by 4
Casciaro, M., Gangemi, S., Caramori, G., Nucera, F., Tuccari, G., & Ieni, A. (2024) · Pathology - Research and Practice · doi:10.1016/j.prp.2024.155208 · Cited by 3
Atamas, S. P., Lockatell, V., Todd, N. W., Papadimitriou, J. C., Rus, V., Lugkey, K. N., Vogel, S. N., Toshchakov, V. Y., & Luzina, I. G. (2024) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.123.002050 · Cited by 3
Kamari‐Kany, N., Weischendorff, S., Ifversen, M., Horan, D. E., Enevold, C., Kielsen, K., & Müller, K. (2025) · Pediatric Blood & Cancer · doi:10.1002/pbc.31995 · Cited by 3
Interleukin-33/ST2: A new signaling pathway in immunity and immunopathology
Pavlovic, S. M., Zdravkovic, N. S., Radosavljevic, G. D., Arsenijević, N., Lukić, M. L., & Jovanović, I. (2012) · Vojnosanitetski pregled · doi:10.2298/vsp1201069p · Cited by 3
Cytokines in liver, biliary, and pancreatic disease
Weiss, M. J. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4377-1454-8.00010-2 · Cited by 3
Turner, M. J. (2017) · Springer eBooks · doi:10.1007/978-3-319-29785-9_15 · Cited by 5
Hematopoietic Growth Factors and Cytokines
Ekmekçioglu, S., Kurzrock, R., & Grimm, E. A. (2015) · Elsevier eBooks · doi:10.1016/b978-1-4557-4066-6.00057-3 · Cited by 5
Hasan, A., Kochumon, S., Al‐Ozairi, E., Tuomilehto, J. O., Al‐Mulla, F., & Ahmad, R. (2020) · Diabetes Metabolic Syndrome and Obesity · doi:10.2147/dmso.s251978 · Cited by 6
Interleukin-33 and Obesity-Related Inflammation and Cancer
Kowitt, C., & Zhang, Q. (2024) · Encyclopedia · doi:10.3390/encyclopedia4040117 · Cited by 3
Zhang, Z., Li, L., Zhao, L., Liu, G., Han, F., Du, J., & Liu, L. (2022) · Translational Pediatrics · doi:10.21037/tp-21-606 · Cited by 2
Jiang, Y., Donati, V. L., Peters, G. J., Giovannetti, E., & Deng, D. (2023) · Cancer Drug Resistance · doi:10.20517/cdr.2023.06 · Cited by 2
Naef, P., Jaeger-Ruckstuhl, C. A., Schnüriger, N., Forster, S., Monteiro, I., Brigger, D., Eggel, A., Kessenbrock, K., Riether, C., & Ochsenbein, A. F. (2025) · iScience · doi:10.1016/j.isci.2025.112378 · Cited by 5
Liu, X., Wu, Y., Chai, J., Su, X., Qu, Y., Hu, F.-C., Liu, T., Zheng, J., Han, S., Zhou, H., et al. (2025) · Burns · doi:10.1016/j.burns.2025.107615 · Cited by 2
New Perspectives on Classical Alarmin Responses to Intestinal Helminth Infection
Lynch, C. P., & Grencis, R. K. (2025) · Parasite Immunology · doi:10.1111/pim.70027 · Cited by 2
Perea, B., Gambini, C., Paggi, I., Biancucci, S., Cattelan, S., Genovese, M., d’Alessandro, M., Cameli, P., Bargagli, E., Dilroba, A., et al. (2025) · Cytokine · doi:10.1016/j.cyto.2025.157080 · Cited by 2
Bui, T. M., Rojas-Jiménez, E. A., Li, Z., Foidart, P., Puleo, J. I., Yan, P., Jhaveri, A., Yang, L., Nishida, J., Seehawer, M., et al. (2026) · Cancer Cell · doi:10.1016/j.ccell.2026.03.015 · Cited by 3
Overview of the Immune System and Immunotoxicology
Lawrence, D. A. (2010) · Elsevier eBooks · doi:10.1016/b978-0-08-046884-6.00601-1 · Cited by 3
Development of Lymph Node Circulation and Homing Mechanisms
Ager, A., Coles, M. C., & Stein, J. V. (2010) · Springer eBooks · doi:10.1007/978-3-642-14429-5_8 · Cited by 2
Lin, T., Chang, P., Lo, C., Lo, Y., Yu, C., Lin, S., Kuo, C. S., & Lin, H. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.823994 · Cited by 2
Baranova, N. S., Gris, M. S., Baranov, A. A., Spirin, N., Artyuhov, A., Шакирова, К. М., & Nasonov, E. (2023) · Bulletin of Russian State Medical University · doi:10.24075/brsmu.2023.032 · Cited by 3
The IL-33/ST2 Axis Affects Adipogenesis Through Regulating the TRAF6/RelA Pathway
Cao, S., Qin, X., Li, C., Zhang, L., Ren, S., Zhou, W., Zhao, M., & Zhou, G. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252212005 · Cited by 2
Obata‐Ninomiya, K., Tharmalingam, J., & Ziegler, S. F. (2024) · Clinical & Translational Immunology · doi:10.1002/cti2.70020 · Cited by 2
Dobrican, C. T., Deleanu, D. M., Iancu, M., Muntean, I. A., Nedelea, I., Bălan, R.-G., Procopciuc, L. M., & Filip, G. A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252413709 · Cited by 3
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Gorbacheva, A. M., & Mitkin, N. A. (2019) · Molecular Biology · doi:10.1134/s0026898419050069 · Cited by 3
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Sánchez-Alavez, M., & Bartfai, T. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0702505104 · Cited by 2
Potential therapeutic targets from genetic and epigenetic approaches for asthma
Zhang, Y. (2016) · World Journal of Translational Medicine · doi:10.5528/wjtm.v5.i1.14 · Cited by 2
Taniguchi, K. (2013) · Journal of Clinical & Experimental Dermatology Research · doi:10.4172/2155-9554.1000183 · Cited by 2
Molecular genetic aspects of polypous rhinosinusitis
Moiseeva, Y. P., & Пискунов, Г. З. (2020) · Russian Rhinology · doi:10.17116/rosrino20202801126 · Cited by 2
Huang, F. P., Chen, W.-Y., Ma, J., He, X., & Wang, J. (2021) · World Journal of Clinical Cases · doi:10.12998/wjcc.v10.i1.23 · Cited by 2
Lewko, W. M., & Oldham, R. K. (2009) · Springer eBooks · doi:10.1007/978-90-481-2289-9_8 · Cited by 2
Ochi, T., Asai, A., Okamura, S., Yamaguchi, H., Ohashi, S., & Mitake, M. (1987) · PubMed · Cited by 2
The role of innate lymphoid cells in the heart and cardiac inflammation
Choi, H. S., Hou, X., Bracamonte‐Baran, W., Diny, N. L., Talor, M. V., & Čiháková, D. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.200.supp.42.22 · Cited by 2
Physiological role of the IL-1 family cytokines and receptors in the human brain
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Advances in targeting IL-1 family cytokines for the treatment of inflammatory diseases
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Immunology of the Asthmatic Response
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The curious case of IL‐33 in homeostasis and infection
Nadafi, R., & Arens, R. (2020) · European Journal of Immunology · doi:10.1002/eji.202049031 · Cited by 1
Agrawal, A. C., Mohapatra, E., Nanda, R., Bodhey, N. K., Sakale, H. S., & Garg, A. K. (2022) · Cureus · doi:10.7759/cureus.23556 · Cited by 1
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PAs and NPs in an emergency room-linked acute care clinic.
Currey, C. J. (1984) · PubMed · Cited by 1
Szabó, G., & Bruneau, J. C. (2013) · Wiley eBooks · doi:10.1002/9781118637272.ch2 · Cited by 1
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Research of Immunology Markers of UC
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Martinovi, M. (2013)
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Bosch, I., & Muñoz‐Jordán, J. L. (2009) · Salus Journal of Health Sciences
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IL-36 member activation and secretion, and their role in immune defence
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Ali, S., & Justus Liebig University Giessen (2009) · University writing server of the Justus Liebig University Giessen (Justus-Liebig-Universität Gießen) · doi:10.22029/jlupub-10134
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 ›
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