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Lipopolysaccharide-mediated Reactive Oxygen Species and Signal Transduction in the Regulation of Interleukin-1 Gene Expression
Open accessAbstract
Lipopolysaccharide (LPS) stimulates macrophages to release inflammatory cytokines, interleukin-1 beta (IL-1), and tumor necrosis factor (TNF). LPS-induced TNF suppresses scavenger receptor functions in macrophages (van Lenten, B. J., and Fogelman, A. M. (1992) J. Immunol. 148, 112-116), which is regulated by TNF-mediated protein kinases (Hsu, H. Y., and Twu, Y. C. (2000) J. Biol. Chem. 275, 41035-41048). To examine the molecular mechanism for LPS induction of IL-1 in macrophages, we demonstrated that LPS quickly stimulated reactive oxygen species (ROS), and 3 h later induced prointerleukin-1 beta (pro-IL-1, precursor of IL-1) production and IL-1 secretion. LPS stimulated pro-IL-1 message/protein between 3 and 10 h; however, there was a 40% reduction of pro-IL-1 in preincubation of the antioxidant, N-acetylcysteine (NAC). Moreover, NAC moderated LPS-induced IL-1 secretion partially via interleukin 1-converting enzyme. The maximal activity of LPS-induced ERK, JNK, and p38 was 12- (30 min), 5- (30 min), and 16-fold (15 min), respectively. In contrast, NAC reduced ERK activity to 60% and decreased p38 activity to the basal level, but JNK activity was induced 2-fold. Furthermore, the pharmacological antagonists LY294002, SB203580, curcumin, calphostin C, and PD98059 revealed the diverse roles of LPS-mediated protein kinases in pro-IL-1. On the other hand, NAC and diphenyleneiodonium chloride partially inhibited LPS-induced Rac activity and protein-tyrosine kinase (PTK), indicating that LPS-mediated ROS and NADPH oxidase correspond to Rac activation and IL-1 expression. Our findings establish for the first time that LPS-mediated PTK/phosphatidylinositol 3-kinase/Rac/p38 pathways play a more important role than pathways of PTK/PKC/MEK/ERK and of PTK/phosphatidylinositol 3-kinase/Rac/JNK in the regulation of pro-IL-1/IL-1. The findings also further elucidate the critical role of LPS-mediated ROS in signal transduction pathways. Our results suggest that understanding LPS-transduced signals in IL-1 induction upon the antibacterial action of macrophages should provide a therapeutic strategy for aberrant inflammatory responses leading to severe cellular injury or concurrent multiorgan septic damage.
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“In the NF-κB system (e.g. [2020-2024]) (Fig 8), NF-κB is normally held inactive in the cytoplasm by binding to an inhibitor IκB (often IκBα). Pro-inflammatory cytokines such as TNF-α, LPS [2025-2030] and IL-1 [2031] act by binding to receptors at the cell surface and initiating signalling pathways that lead to the activation of a particular kinase, IκB kinase or IKK. This kinase phosphorylates the”
From Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases (2009) · cites this paper as [2027]
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Kemelo, M. K., Canová, N. K., Hořínek, A., & Farghali, H. (2017) · Physiological Research · doi:10.33549/physiolres.933488 · Cited by 13
“BRUNET A, SWEENEY LB, STURGILL JF, CHUA KF, GREER PL, LIN Y, TRAN H, ROSS SE, MOSTOSLAVSKY R, COHEN HY, ET AL.”
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“Because antioxidants have previously been shown to inhibit cytokine production from monocytes (Haddad and Land, 2002; Hsu and Wen, 2002), we evaluated if the inhibitory effect of AGIX- 4207 on cytokine production that was observed in ECs and FLSs extended to PBMCs.”
BackgroundInfluentialFunctional roles and cancer variants of the bifunctional glycosylase NEIL2
Hua, A., & Sweasy, J. B. (2023) · Environmental and Molecular Mutagenesis · doi:10.1002/em.22555 · Cited by 12
“However, when there's a significant increase in ROS level, Sp1 undergoes oxidative degradation that decreases its availability for binding to the promoter thereby resulting in downregulation of the NEIL2 (Chakraborti et al., 2017).”
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“The LPSinduced generation of free radicals in microglia was an upstream event serving to regulate the production of other proinflammatory factors [17, 18].”
BackgroundKleber, A., Altmeyer, S., Wolf, B., Wolf, A., Volk, T. J., Fink, T., & Kubulus, D. (2014) · Inflammation Research · doi:10.1007/s00011-014-0779-4 · Cited by 12
“On the other hand, Hsu and Wen concluded that p38 pathways are more important for LPSinduced regulation of IL-1b in macrophages than ERK or JNK signaling [42].”
Hironao, K.-Y., Ashida, H., & Yamashita, Y. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1006132 · Cited by 11
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“Because oxidative activity is one of the factors related to the power to sterilize bacteria, its reduction is associated with immune dysfunction and high mortality (32, 33).”
BackgroundIn Vitro and In Vivo Anti-Inflammatory Effects of Cannabis sativa Stem Extract
Kim, Y. N., Sim, K. S., Park, S., Sohn, H.-Y., Kim, T., & Kim, J. H. (2022) · Journal of Medicinal Food · doi:10.1089/jmf.2021.k.0200 · Cited by 11
“29,30 Therefore, a number of studies using natural antioxidants or medicinal plant extracts have targeted the reduction of intracellular ROS in macrophages and/or animal models to demonstrate their anti-inflammatory effects.”
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“It is known that LPS-induced cytokines are a potent activator of macrophages and stimulate ROS production such as H2O2, NO (36), and superoxides (37).”
BackgroundCKBM stimulates MAPKs but inhibits LPS-induced IFN-γ in lymphocytes
Chan, A. S. L., Yip, E. C. H., Yung, L. Y., Pang, H., Luk, S. C. W., Pang, S. F., & Wong, Y. H. (2006) · Phytotherapy Research · doi:10.1002/ptr.1943 · Cited by 11
“IL-1β is a cytokine primarily produced by monocytes and macrophages (Hsu and Wen, 2002).”
Matos, T. J., Jaleco, S. P., Gonçalo, M., Duarte, C. B., & Lopes, M. C. (2005) · Mediators of Inflammation · doi:10.1155/mi.2005.131 · Cited by 11
“FSDCs (0.2×106 cells/well) were cultured in a 48-well microplate and were incubated for 30 minutes in the presence or absence of DNFB (1 µg/mL), DCNB (1 µg/mL), or GM-CSF (10 ng/mL), or for 12 hours in the presence of LPS (40 µg/mL).”
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Edirisinghe, D. I. U., Singh, A., Seitz, M. P., Esmaeili, A. J., Orado, T. K., Herrero, E., Jankowski, J., Kairuki, P. K., Marshall, L. R., Jain, E., et al. (2025) · ACS Applied Bio Materials · doi:10.1021/acsabm.5c00092 · Cited by 12
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“Pathogen-sensitized macrophages produce excessive ROS, accelerating immune reactions [52].”
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“The importance of the antioxidant mechanism of NAC and its antiinflammatory effect is emphasized in reference to a report in which NAC inhibits LPS-induced cytokine activation [30].”
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Reactive oxygen species mediate phorbol ester-stimulated cAMP response in human eosinophils
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Spatiotemporal proteomic profiling of cellular responses to NLRP3 agonistsPreprint
Hollingsworth, L. R., Veeraraghavan, P., Paulo, J. A., & Harper, J. W. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.19.590338 · Cited by 10
Dissemination of pathogenic bacteria is reinforced by a MARTX toxin effector duet
Choi, S.-H., Lee, Y., Park, S., Jang, S. Y., Park, J., Oh, D. W., Kim, S., Kim, T., Lee, G. S., Cho, C., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-50650-0 · Cited by 8
“The intracellular ROS levelincreased upon infection with EF or inactive RDTND-containing toxin strains (EF::RDTND E/Q -RID C/A ) due to LPS-mediated ROS generation 33,44 ; however, infection by the EF::RDTND-RID C/A strain reduced ROS production by macrophages signi fi cantly.”
Metadata
- Authors
- Hsu, H.-Y., & Wen, M.-H.
- Affiliations
- National Yang Ming University (TW)
- Corresponding author
- Hsu, Hsien-Yeh
- ORCID
- Wen, Meng-Hsuan
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2002-06
- Volume
- 277
- Issue
- 25
- Pages
- 22131-22139
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W2016146035
- Cited by
- 519
- References
- 72
- Citations by year
- 2026: 13 · 2025: 17 · 2024: 20 · 2023: 21 · 2022: 21 · 2021: 27 · 2020: 22 · 2019: 23 · 2018: 25 · 2017: 33 · 2016: 27 · 2015: 21 · 2014: 18 · 2013: 19 · 2012: 14
- FWCI
- 7.22
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Keywords
- lipopolysaccharide, IL-1β, reactive oxygen species, N-acetylcysteine, macrophages, Rac, p38 MAPK, JNK, ERK, phosphatidylinositol 3-kinase, tyrosine kinase, NADPH oxidase, signal transduction, inflammatory cytokines, TNF-α
- MeSH terms
- Animals, Carrier Proteins, Cell Line, Chromones, Curcumin, Enzyme Activation, Enzyme Inhibitors, Enzyme-Linked Immunosorbent Assay, Flavonoids, Gene Expression Regulation, Genes, Dominant, Imidazoles, Interleukin-1, Lipopolysaccharides, Macrophages, Models, Biological, Morpholines, Naphthalenes, Oxygen, Protein Binding, Pyridines, Time Factors, Transfection, Signal Transduction, Reactive Oxygen Species, rac1 GTP-Binding Protein, Mitogen-Activated Protein Kinases, Mitogen-Activated Protein Kinase Kinases, Intracellular Signaling Peptides and Proteins, JNK Mitogen-Activated Protein Kinases, p38 Mitogen-Activated Protein Kinases, MAP Kinase Kinase 4, Mice
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