O-GlcNAcylation Modification in Immune Cells: Potential Therapeutic Implications of Sepsis
O-GlcNAc modification is a glycosylation modification that is commonly observed in nuclear and organelle proteins of cells. In recent years, several studies have shown that O-GlcNAc modification plays an important regulatory role in immune cells, which regulates their activity and function and inhib...
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Published in | Intensive care research Vol. 3; no. 3; pp. 204 - 214 |
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Main Authors | , |
Format | Journal Article |
Language | English |
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01.09.2023
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Abstract | O-GlcNAc modification is a glycosylation modification that is commonly observed in nuclear and organelle proteins of cells. In recent years, several studies have shown that O-GlcNAc modification plays an important regulatory role in immune cells, which regulates their activity and function and inhibits inflammatory responses. It also enhances immune cells recognition and clearance of pathogens, and improves the host´s antibacterial immune response. Sepsis is a systemic inflammatory response to infection, whose development and progression are regulated by the immune system. Therefore, in the present review, we will discuss the mechanism of O-GlcNAc modification in immune cells and its potential therapeutic value in sepsis, which will be expected to provide new insights and targets for the treatment of sepsis. |
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AbstractList | O-GlcNAc modification is a glycosylation modification that is commonly observed in nuclear and organelle proteins of cells. In recent years, several studies have shown that O-GlcNAc modification plays an important regulatory role in immune cells, which regulates their activity and function and inhibits inflammatory responses. It also enhances immune cells recognition and clearance of pathogens, and improves the host´s antibacterial immune response. Sepsis is a systemic inflammatory response to infection, whose development and progression are regulated by the immune system. Therefore, in the present review, we will discuss the mechanism of O-GlcNAc modification in immune cells and its potential therapeutic value in sepsis, which will be expected to provide new insights and targets for the treatment of sepsis. Abstract O-GlcNAc modification is a glycosylation modification that is commonly observed in nuclear and organelle proteins of cells. In recent years, several studies have shown that O-GlcNAc modification plays an important regulatory role in immune cells, which regulates their activity and function and inhibits inflammatory responses. It also enhances immune cells recognition and clearance of pathogens, and improves the host´s antibacterial immune response. Sepsis is a systemic inflammatory response to infection, whose development and progression are regulated by the immune system. Therefore, in the present review, we will discuss the mechanism of O-GlcNAc modification in immune cells and its potential therapeutic value in sepsis, which will be expected to provide new insights and targets for the treatment of sepsis. |
Author | Huang, ZhenZhen Qin, YuanMei |
Author_xml | – sequence: 1 givenname: ZhenZhen surname: Huang fullname: Huang, ZhenZhen organization: Department of Emergency Medicine, Zhoukou Central Hospital – sequence: 2 givenname: YuanMei surname: Qin fullname: Qin, YuanMei email: Qinyuanmei69@163.com organization: Henan University of Chinese Medicine |
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Cites_doi | 10.1177/0271678X16679671 10.1111/bph.12223 10.1038/nrm.2017.22 10.4037/ajcc2016432 10.3390/metabo12080725 10.3390/ijms22179236 10.3390/cells10112962 10.1016/j.biopha.2021.111477 10.3389/fcimb.2017.00373 10.3390/ijms21072356 10.1074/jbcM116.766568 10.1111/mmi.13849 10.1074/jbc.M116.737940 10.1128/MMBR.00027-07 10.4049/jimmunol.0903151 10.1097/WNR.0000000000001582 10.1016/j.clim.2004.08.015 10.1186/s13073-019-0674-2 10.3389/fphys.2019.01614 10.3389/fimmu.2016.00155 10.1016/j.cell.2016.05.056 10.1146/annurev-physiol-061121-040214 10.1021/acschembio.7b00869 10.1097/CCM.0000000000002380 10.1016/j.ejphar.2020.173090 10.1038/s41388-018-0435-5 10.1038/s41598-019-55381-7 10.1371/journal.ppat.1004701 10.1016/j.intimp.2021.107791 10.2174/1389203720666190305164128 10.2174/1871529x15666150108113236 10.3389/fimmu.2022.841299 10.1038/sj.emboj.7601845 10.1128/JB.00234-06 10.1038/ncomms12526 10.1016/j.immuni.2019.01.007 10.1073/pnas.1521740112 10.4049/jimmunol.181.8.5481 10.1371/journal.ppat.1003080 10.4049/jimmunol.175.12.8003 10.3389/fendo.2022.943576 10.1016/j.bbagen.2013.09.011 10.1038/s41568-018-0090-8 10.1111/imm.12854 10.1016/S0021-9258(17)43295-9 10.1016/j.jaci.2013.01.046 10.3390/cancers13071666 10.3390/ijms231911260 10.1146/annurev.Immunol.021908.132706 10.1073/pnas.1214550110 10.1073/pnas.1801850115 10.1007/s12017-019-08584-0 10.1001/jama.2016.0287 10.1002/cyto.a.20569 10.4049/jimmunol.1302259 10.1097/01.shk.0000068322.08268.b4 10.1038/ni.3439 10.1038/nm0509-496 10.4161/viru.26516 10.1038/s41590-020-0789-z 10.1074/jbc.RA119.008373 10.1007/s00011-016-0970-x 10.1111/cmi.12304 10.1111/febs.14491 10.1084/jem.20161105 10.1074/jbc.RA118.004638 10.3390/ijms23126430 10.1073/pnas.1323226111 10.1038/s41467-018-04719-2 10.1073/pnas.2119658120 10.1074/jbc.M414066200 10.1038/sj.cr.7290215 10.3389/fimmu.2021.701675 10.1152/physrev.00043.2019 10.1038/s41467-019-08300-3 10.1016/s1074-7613(02)00333-3 10.1038/s41467-017-01677-z 10.1007/s10863-017-9735-7 10.4049/jimmunol.1601727 10.1177/154411130201300302 10.1007/s10863-018-9744-1 10.1152/ajpcell.00042.2013 10.1128/JB.01175-10 10.1126/scisignal.20040 10.1074/jbc.M407911200 10.1073/pnas.0405821101 10.1016/j.redox.2022.102581 |
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References | Kneass, Marchase (CR59) 2004 Lorente-Sorolla, Garcia-Gomez, Català-Moll (CR6) 2019 von Knethen, Heinicke, Weigert (CR20) 2020 Hwang, Kim, Park (CR55) 2019 Vatanen, Kostic (CR73) 2016 Chatham, Zhang, Wende (CR24) 2021 Lo, Shie, Chen (CR68) 2018 Yao, Tang, Wang (CR63) 2004 Boamah, Gilmore, Bourget (CR83) 2023 Singer, Deutschman, Seymour (CR1) 2016 Wesselkamper, Eppert, Motz (CR72) 2008 Torres, Hart (CR21) 1984; 259 Golks, Tran, Goetschy (CR32) 2007 Nedeva, Menassa, Duan (CR11) 2020 Cicchetti, Allen, Glogauer (CR62) 2002 Feinberg, Ramakrishnan, Wong (CR70) 2022 Chen, Liu, Gao (CR54) 2021 Li, Zhang, Li (CR52) 2017 Silva-Aguiar, Peruchetti, Pinheiro (CR7) 2022 Hwang, Kwon, Kim (CR49) 2017 Liu, Dong, Li (CR27) 2022 Johnson, Opimba, Bernier (CR35) 2014 Chu, Lo, Yeh (CR67) 2014 Lerman, Kim (CR56) 2015 Kneass, Marchase (CR61) 2005 Shah, Zúñiga-Pflücker (CR30) 2014 Liu, Ma, Chen (CR36) 2017 Cao, Schnelzer, Hannemann (CR4) 2021 van der Laarse, Leney, Heck (CR31) 2018 Yang, Qian (CR25) 2017 Lockridge, Hanover (CR22) 2022 Wheeler, Chevalier, Eberl (CR82) 2014 He, Ma, Li, Thiamet (CR48) 2017 Wang, Lu, Zheng (CR77) 2021 Vatanen, Kostic (CR13) 2016; 4 Bhan, Dipankar, Chakraborty (CR19) 2016 Nguyen, Green, Mecsas (CR12) 2017 Ma, Chalkley, Vosseller (CR33) 2017 Swamy, Pathak, Grzes (CR29) 2016 Pieper, Grimbacher, Eibel (CR42) 2013 Yunna, Mengru, Lei (CR53) 2020 Pachot, Monneret, Voirin (CR18) 2005 Hotchkiss, Coopersmith, McDunn (CR3) 2009 Ferron, Cadiet, Persello (CR8) 2019 Parker, Peterson, Slawson (CR26) 2021 Hwang, Hwang, Kim (CR46) 2013 Dupas, Persello, Blangy-Letheule (CR79) 2022 Wu, Su, Zha (CR78) 2023 Guo, Patil, Luan (CR71) 2018 Denis, Dupas, Persello (CR76) 2021 Sohanpal, El-Labany, Lahooti (CR88) 2004 Wu, Wu, Tsai (CR44) 2016 Sônego, Castanheira, Ferreira (CR57) 2016 Jamieson, Diefenbach, McMahon (CR64) 2002 Silva, Olivon, Mestriner (CR75) 2019 Qiu, Tu, Ju (CR9) 2019 Wu, Chiang, Hsu (CR43) 2017 Korgaonkar, Whiteley (CR80) 2011 Wiesner, Specht, Lee (CR86) 2015 Torres, Pickkers, van der Poll (CR2) 2022 Janas, Groves, Kienzle (CR40) 2005 Madsen-Bouterse, Xu, Petty (CR58) 2008 Barnhart, Lynem, Chapman (CR89) 2006 Shankar-Hari, Fear, Lavender (CR45) 2017 Jiang, Xu, Li (CR65) 2019 Bueter, Specht, Levitz (CR85) 2013 Unsinger, McGlynn, Kasten (CR15) 2010 Ferron, Cadiet, Persello (CR74) 2019 Sharma, Saluja, Banerjee (CR23) 2018 Hwang, Hwang, Kim (CR47) 2013 Korgaonkar, Trivedi, Rumbaugh (CR87) 2013 Ramakrishnan, Clark, Mason (CR34) 2013 Smith-Garvin, Koretzky, Jordan (CR39) 2009 Liu, Salgado, Singh (CR38) 2019 Lopez Aguilar, Gao, Hou (CR41) 2017 Boomer, Green, Hotchkiss (CR10) 2014 Park, Lai, Arumugam (CR28) 2020 Yin, Leavenworth, Li (CR66) 2015 Hynninen, Pettilä, Takkunen (CR14) 2003 Machacek, Slawson, Fields (CR16) 2018 Machacek, Saunders, Zhang (CR37) 2019 Loftus, Assmann, Kedia-Mehta (CR69) 2018 Greathouse, Hall (CR17) 2016 Huynh, Chand, Gough (CR51) 2019 Li, Gong, Wang (CR50) 2019 Santarsiero, Convertini, Todisco (CR5) 2021 Cong, Sun, Yang (CR60) 2021 Park, Uehara (CR81) 2008 Bonnet, Durmort, Jacq (CR84) 2017 C Liu (48_CR27) 2022 JL Wu (48_CR44) 2016 Y Guo (48_CR71) 2018 A Pachot (48_CR18) 2005 SA Madsen-Bouterse (48_CR58) 2008 CL Bueter (48_CR85) 2013 MP Parker (48_CR26) 2021 B Liu (48_CR38) 2019 A Santarsiero (48_CR5) 2021 A Korgaonkar (48_CR87) 2013 JT Park (48_CR81) 2008 C Nedeva (48_CR11) 2020 F Sônego (48_CR57) 2016 A Lopez Aguilar (48_CR41) 2017 K Pieper (48_CR42) 2013 JC Chatham (48_CR24) 2021 J Unsinger (48_CR15) 2010 J Wang (48_CR77) 2021 D Wu (48_CR78) 2023 RP Silva-Aguiar (48_CR7) 2022 GT Nguyen (48_CR12) 2017 R Liu (48_CR36) 2017 R Wheeler (48_CR82) 2014 M Swamy (48_CR29) 2016 S van der Laarse (48_CR31) 2018 AK Korgaonkar (48_CR80) 2011 J Huynh (48_CR51) 2019 Y Qiu (48_CR9) 2019 JF Silva (48_CR75) 2019 SC Wesselkamper (48_CR72) 2008 A Golks (48_CR32) 2007 X Yang (48_CR25) 2017 JS Boomer (48_CR10) 2014 M Denis (48_CR76) 2021 BK Sohanpal (48_CR88) 2004 M Machacek (48_CR16) 2018 DK Shah (48_CR30) 2014 ZT Kneass (48_CR61) 2005 ML Janas (48_CR40) 2005 ZT Kneass (48_CR59) 2004 T Dupas (48_CR79) 2022 J Yin (48_CR66) 2015 PW Lo (48_CR68) 2018 SY Hwang (48_CR46) 2013 AM Jamieson (48_CR64) 2002 CR Torres (48_CR21) 1984; 259 RS Hotchkiss (48_CR3) 2009 M Ferron (48_CR74) 2019 JS Hwang (48_CR55) 2019 G Cicchetti (48_CR62) 2002 M Singer (48_CR1) 2016 JS Hwang (48_CR49) 2017 R Cong (48_CR60) 2021 X Li (48_CR52) 2017 LK Torres (48_CR2) 2022 J Bonnet (48_CR84) 2017 M Shankar-Hari (48_CR45) 2017 T Vatanen (48_CR73) 2016 JL Wu (48_CR43) 2017 DL Wiesner (48_CR86) 2015 T Vatanen (48_CR13) 2016; 4 A von Knethen (48_CR20) 2020 B Johnson (48_CR35) 2014 M Ferron (48_CR8) 2019 NS Sharma (48_CR23) 2018 MM Barnhart (48_CR89) 2006 X Chen (48_CR54) 2021 AY Yao (48_CR63) 2004 CS Chu (48_CR67) 2014 A Lockridge (48_CR22) 2022 C Lorente-Sorolla (48_CR6) 2019 C Bhan (48_CR19) 2016 M Hynninen (48_CR14) 2003 X Li (48_CR50) 2019 S Cao (48_CR4) 2021 M Machacek (48_CR37) 2019 RM Loftus (48_CR69) 2018 JE Smith-Garvin (48_CR39) 2009 D Feinberg (48_CR70) 2022 J Park (48_CR28) 2020 M Jiang (48_CR65) 2019 Z Ma (48_CR33) 2017 P Ramakrishnan (48_CR34) 2013 SY Hwang (48_CR47) 2013 Y He (48_CR48) 2017 C Yunna (48_CR53) 2020 D Boamah (48_CR83) 2023 KC Greathouse (48_CR17) 2016 YV Lerman (48_CR56) 2015 |
References_xml | – year: 2017 ident: CR48 article-title: Mediates neuroprotection in experimental stroke by modulating microglia/macrophage polarization and inhibiting NF-κB p65 signaling publication-title: J Cereb Blood Flow Metab doi: 10.1177/0271678X16679671 – year: 2013 ident: CR47 article-title: O-GlcNAcylation and p50/p105 binding of c-Rel are dynamically regulated by LPS and glucosamine in BV2 microglia cells publication-title: Br J Pharmacol doi: 10.1111/bph.12223 – year: 2017 ident: CR25 article-title: Protein O-GlcNAcylation: emerging mechanisms and functions publication-title: Nat Rev Mol Cell Biol doi: 10.1038/nrm.2017.22 – year: 2016 ident: CR17 article-title: Critical Illness-induced immune suppression: current state of the science publication-title: Am J Crit Care doi: 10.4037/ajcc2016432 – year: 2022 ident: CR27 article-title: O-GlcNAc modification and its role in diabetic retinopathy publication-title: Metabolites doi: 10.3390/metabo12080725 – year: 2021 ident: CR76 article-title: An -GlcNAcylomic approach reveals ACLY as a potential target in sepsis in the young rat publication-title: Int J Mol Sci doi: 10.3390/ijms22179236 – year: 2021 ident: CR5 article-title: ACLY nuclear translocation in human macrophages drives proinflammatory gene expression by NF-κB acetylation publication-title: Cells doi: 10.3390/cells10112962 – year: 2021 ident: CR60 article-title: Protein O-GlcNAcylation alleviates small intestinal injury induced by ischemia-reperfusion and oxygen-glucose deprivation publication-title: Biomed Pharmacother. doi: 10.1016/j.biopha.2021.111477 – year: 2017 ident: CR12 article-title: Neutrophils to the ROScue: mechanisms of NADPH oxidase activation and bacterial resistance publication-title: Front Cell Infect Microbiol doi: 10.3389/fcimb.2017.00373 – year: 2020 ident: CR20 article-title: Histone deacetylation inhibitors as modulators of regulatory T cells publication-title: Int J Mol Sci doi: 10.3390/ijms21072356 – year: 2017 ident: CR33 article-title: Hyper- -GlcNAcylation activates nuclear factor κ-light-chain-enhancer of activated B cells (NF-κB) signaling through interplay with phosphorylation and acetylation publication-title: J Biol Chem doi: 10.1074/jbcM116.766568 – year: 2017 ident: CR84 article-title: Peptidoglycan -acetylation is functionally related to cell wall biosynthesis and cell division in Streptococcus pneumoniae publication-title: Mol Microbiol doi: 10.1111/mmi.13849 – year: 2017 ident: CR49 article-title: Lipopolysaccharide (LPS)-stimulated iNOS induction is increased by glucosamine under normal glucose conditions but is inhibited by glucosamine under high glucose conditions in macrophage cells publication-title: J Biol Chem doi: 10.1074/jbc.M116.737940 – year: 2008 ident: CR81 article-title: How bacteria consume their own exoskeletons (turnover and recycling of cell wall peptidoglycan) publication-title: Microbiol Mol Biol Rev doi: 10.1128/MMBR.00027-07 – year: 2010 ident: CR15 article-title: IL-7 promotes T cell viability, trafficking, and functionality and improves survival in sepsis publication-title: J Immunol doi: 10.4049/jimmunol.0903151 – year: 2021 ident: CR77 article-title: Glutamine's protection against brain damage in septic rats via increased protein oxygen- -acetylglucosamine modification publication-title: NeuroReport doi: 10.1097/WNR.0000000000001582 – year: 2005 ident: CR18 article-title: Longitudinal study of cytokine and immune transcription factor mRNA expression in septic shock publication-title: Clin Immunol doi: 10.1016/j.clim.2004.08.015 – year: 2019 ident: CR6 article-title: Inflammatory cytokines and organ dysfunction associate with the aberrant DNA methylome of monocytes in sepsis publication-title: Genome Med doi: 10.1186/s13073-019-0674-2 – year: 2019 ident: CR75 article-title: Acute increase in -GlcNAc improves survival in mice with LPS-induced systemic inflammatory response syndrome publication-title: Front Physiol doi: 10.3389/fphys.2019.01614 – year: 2016 ident: CR57 article-title: Paradoxical roles of the neutrophil in sepsis: protective and deleterious publication-title: Front Immunol doi: 10.3389/fimmu.2016.00155 – year: 2016 ident: CR73 article-title: Variation in microbiome LPS immunogenicity contributes to autoimmunity in humans publication-title: Cell. doi: 10.1016/j.cell.2016.05.056 – year: 2022 ident: CR2 article-title: Sepsis-Induced Immunosuppression publication-title: Annu Rev Physiol doi: 10.1146/annurev-physiol-061121-040214 – year: 2017 ident: CR41 article-title: Profiling of protein -GlcNAcylation in murine CD8(+) effector− and memory-like T cells publication-title: ACS Chem Biol doi: 10.1021/acschembio.7b00869 – year: 2017 ident: CR45 article-title: Activation—associated accelerated apoptosis of memory B cells in critically ill patients with sepsis publication-title: Crit Care Med doi: 10.1097/CCM.0000000000002380 – year: 2020 ident: CR53 article-title: Macrophage M1/M2 polarization publication-title: Eur J Pharmacol doi: 10.1016/j.ejphar.2020.173090 – year: 2019 ident: CR65 article-title: O-GlcNAcylation promotes colorectal cancer metastasis via the miR-101-O-GlcNAc/EZH2 regulatory feedback circuit publication-title: Oncogene doi: 10.1038/s41388-018-0435-5 – year: 2019 ident: CR8 article-title: O-GlcNAc stimulation: a new metabolic approach to treat septic shock publication-title: Sci Rep doi: 10.1038/s41598-019-55381-7 – year: 2015 ident: CR86 article-title: Chitin recognition via chitotriosidase promotes pathologic type-2 helper T cell responses to cryptococcal infection publication-title: PLoS Pathog doi: 10.1371/journal.ppat.1004701 – year: 2021 ident: CR54 article-title: The roles of macrophage polarization in the host immune response to sepsis publication-title: Int Immunopharmacol doi: 10.1016/j.intimp.2021.107791 – year: 2019 ident: CR9 article-title: The immune system regulation in sepsis: from innate to adaptive publication-title: Curr Protein Pept Sci doi: 10.2174/1389203720666190305164128 – year: 2015 ident: CR56 article-title: Neutrophil migration under normal and sepsis conditions publication-title: Cardiovasc Hematol Disord Drug Targets doi: 10.2174/1871529x15666150108113236 – year: 2022 ident: CR70 article-title: Inhibition of -GlcNAcylation decreases the cytotoxic function of natural killer cells publication-title: Front Immunol doi: 10.3389/fimmu.2022.841299 – year: 2007 ident: CR32 article-title: Requirement for -linked -acetylglucosaminyltransferase in lymphocytes activation publication-title: EMBO J doi: 10.1038/sj.emboj.7601845 – year: 2006 ident: CR89 article-title: GlcNAc-6P levels modulate the expression of Curli fibers by publication-title: J Bacteriol doi: 10.1128/JB.00234-06 – year: 2016 ident: CR44 article-title: Temporal regulation of Lsp1 -GlcNAcylation and phosphorylation during apoptosis of activated B cells publication-title: Nat Commun doi: 10.1038/ncomms12526 – year: 2019 ident: CR50 article-title: O-GlcNAc transferase suppresses inflammation and necroptosis by targeting receptor-interacting serine/threonine-protein kinase 3 publication-title: Immunity doi: 10.1016/j.immuni.2019.01.007 – year: 2015 ident: CR66 article-title: Ezh2 regulates differentiation and function of natural killer cells through histone methyltransferase activity publication-title: Proc Natl Acad Sci US A doi: 10.1073/pnas.1521740112 – year: 2008 ident: CR72 article-title: NKG2D is critical for NK cell activation in host defense against pseudomonas aeruginosa respiratory infection publication-title: J Immunol doi: 10.4049/jimmunol.181.8.5481 – year: 2013 ident: CR85 article-title: Innate sensing of chitin and chitosan publication-title: PLoS Pathog doi: 10.1371/journal.ppat.1003080 – year: 2005 ident: CR40 article-title: IL-2 regulates perforin and granzyme gene expression in CD8+ T cells independently of its effects on survival and proliferation publication-title: J Immunol doi: 10.4049/jimmunol.175.12.8003 – year: 2022 ident: CR22 article-title: A nexus of lipid and O-Glcnac metabolism in physiology and disease publication-title: Front Endocrinol (Lausanne) doi: 10.3389/fendo.2022.943576 – year: 2014 ident: CR35 article-title: Implications of the O-GlcNAc modification in the regulation of nuclear apoptosis in T cells publication-title: Biochim Biophys Acta doi: 10.1016/j.bbagen.2013.09.011 – year: 2019 ident: CR51 article-title: Therapeutically exploiting STAT3 activity in cancer—using tissue repair as a road map publication-title: Nat Rev Cancer doi: 10.1038/s41568-018-0090-8 – year: 2018 ident: CR71 article-title: The biology of natural killer cells during sepsis publication-title: Immunology doi: 10.1111/imm.12854 – volume: 259 start-page: 3308 issue: 5 year: 1984 end-page: 17 ident: CR21 article-title: Topography and polypeptide distribution of terminal -acetylglucosamine residues on the surfaces of intact lymphocytes evidence for O-linked GlcNAc publication-title: J Biol Chem. doi: 10.1016/S0021-9258(17)43295-9 – year: 2013 ident: CR42 article-title: B-cell biology and development publication-title: J Allergy Clin Immunol doi: 10.1016/j.jaci.2013.01.046 – year: 2021 ident: CR26 article-title: O-GlcNAcylation and O-GlcNAc cycling regulate gene transcription: emerging roles in cancer publication-title: Cancers (Basel) doi: 10.3390/cancers13071666 – year: 2022 ident: CR7 article-title: O-GlcNAcylation in renal (Patho)physiology publication-title: Int J Mol Sci doi: 10.3390/ijms231911260 – year: 2009 ident: CR39 article-title: T cell activation publication-title: Annu Rev Immunol doi: 10.1146/annurev.Immunol.021908.132706 – year: 2013 ident: CR87 article-title: Community surveillance enhances virulence during polymicrobial infection publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.1214550110 – year: 2018 ident: CR68 article-title: -GlcNAcylation regulates the stability and enzymatic activity of the histone methyltransferase EZH2 publication-title: Natl Acad Sci USA doi: 10.1073/pnas.1801850115 – year: 2020 ident: CR28 article-title: O-GlcNAcylation as a therapeutic target for Alzheimer’s disease publication-title: Neuromo-lecular Med doi: 10.1007/s12017-019-08584-0 – year: 2019 ident: CR74 article-title: O-GlcNAc stimulation: a new metabolic approach to treat septic shock publication-title: Sci Rep doi: 10.1038/s41598-019-55381-7 – year: 2016 ident: CR1 article-title: The third international consensus definitions for sepsis and septic shock (Sepsis-3) publication-title: JAMA doi: 10.1001/jama.2016.0287 – year: 2008 ident: CR58 article-title: Quantification of -GlcNAc protein modification in neutrophils by flow cytometry publication-title: Cytometry A doi: 10.1002/cyto.a.20569 – year: 2014 ident: CR30 article-title: An overview of the intrathymic intricacies of T cell development publication-title: J Immunol doi: 10.4049/jimmunol.1302259 – year: 2003 ident: CR14 article-title: Predictive value of monocyte histocompatibility leukocyte antigen-DR expression and plasma interleukin-4 and -10 levels in critically ill patients with sepsis[J] publication-title: Shock doi: 10.1097/01.shk.0000068322.08268.b4 – year: 2016 ident: CR29 article-title: Glucose and glutamine fuel protein O-GlcNAcylation to control T cell self-renewal and malignancy publication-title: Nat Immunol doi: 10.1038/ni.3439 – year: 2009 ident: CR3 article-title: The sepsis seesaw: tilting toward immunosuppression publication-title: Nat Med doi: 10.1038/nm0509-496 – year: 2014 ident: CR10 article-title: The changing immune system in sepsis: is individualized immuno-modulatory therapy the answer? publication-title: Virulence doi: 10.4161/viru.26516 – year: 2020 ident: CR11 article-title: TREML4 receptor regulates inflammation and innate immune cell death during polymicrobial sepsis publication-title: Nat Immunol doi: 10.1038/s41590-020-0789-z – year: 2019 ident: CR37 article-title: Elevated -GlcNAcylation enhances pro-inflammatory Th17 function by altering the intracellular lipid microenvironment publication-title: J Biol Chem doi: 10.1074/jbc.RA119.008373 – year: 2016 ident: CR19 article-title: Role of cellular events in the pathophysiology of sepsis publication-title: Inflamm Res doi: 10.1007/s00011-016-0970-x – year: 2014 ident: CR82 article-title: The biology of bacterial peptidoglycans and their impact on host immunity and physiology publication-title: Cell Microbiol doi: 10.1111/cmi.12304 – year: 2018 ident: CR31 article-title: Crosstalk between phosphorylation and O-GlcNAcylation: friend or foe publication-title: FEBS J doi: 10.1111/febs.14491 – year: 2017 ident: CR52 article-title: Myeloid-derived cullin 3 promotes STAT3 phosphorylation by inhibiting OGT expression and protects against intestinal inflammation publication-title: J Exp Med doi: 10.1084/jem.20161105 – year: 2019 ident: CR55 article-title: Glucosamine improves survival in a mouse model of sepsis and attenuates sepsis-induced lung injury and inflammation publication-title: J Biol Chem doi: 10.1074/jbc.RA118.004638 – year: 2022 ident: CR79 article-title: Beneficial effects of O-GlcNAc stimulation in a young rat model of sepsis: beyond modulation of gene expression publication-title: Int J Mol Sci doi: 10.3390/ijms23126430 – year: 2014 ident: CR67 article-title: O-GlcNAcylation regulates EZH2 protein stability and function publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.1323226111 – year: 2018 ident: CR69 article-title: Amino acid-dependent cMyc expression is essential for NK cell metabolic and functional responses in mice publication-title: Nat Commun doi: 10.1038/s41467-018-04719-2 – year: 2023 ident: CR83 article-title: Peptidoglycan deacetylation controls type IV secretion and the intracellular survival of the bacterial pathogen Legionella pneumophila publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.2119658120 – volume: 4 start-page: 07 year: 2016 ident: CR13 article-title: Variation in microbiome LPS immunogenicity contributes to autoimmunity in humans publication-title: Cell. – year: 2005 ident: CR61 article-title: Protein -GlcNAc modulates motility-associated signaling intermediates in neutrophils publication-title: J Biol Chem doi: 10.1074/jbc.M414066200 – year: 2004 ident: CR63 article-title: Inhibition of the activating signals in NK92 cells by recombinant GST-sHLA-G1a chain publication-title: Cell Res doi: 10.1038/sj.cr.7290215 – year: 2021 ident: CR4 article-title: The transcription factor FRA-1/AP-1 controls lipocalin-2 expression and inflammation in sepsis model publication-title: Front Immunol doi: 10.3389/fimmu.2021.701675 – year: 2021 ident: CR24 article-title: Role of O-linked -acetylglucosamine protein modification in cellular (patho)physiology publication-title: Physiol Rev doi: 10.1152/physrev.00043.2019 – year: 2019 ident: CR38 article-title: The lineage stability and suppressive program of regulatory T cells require protein O-GlcNAcylation publication-title: Nat Commun doi: 10.1038/s41467-019-08300-3 – year: 2002 ident: CR64 article-title: The role of the NKG2D immunoreceptor in immune cell activation and natural killing publication-title: Immunity doi: 10.1016/s1074-7613(02)00333-3 – year: 2017 ident: CR43 article-title: -GlcNAcylation is required for B cell homeostasis and antibody responses publication-title: Nat Commun doi: 10.1038/s41467-017-01677-z – year: 2018 ident: CR23 article-title: Nutrient-sensing and self-renewal: O-GlcNAc in a new role publication-title: J Bioenerg Biomembr doi: 10.1007/s10863-017-9735-7 – year: 2017 ident: CR36 article-title: MicroRNA-15b suppresses 17th differentiation and is associated with pathogenesis of multiple sclerosis by targeting O-GlcNAc transferase publication-title: J Immunol doi: 10.4049/jimmunol.1601727 – year: 2002 ident: CR62 article-title: Chemotactic signaling pathways in neutrophils: from receptor to actin assembly publication-title: Crit Rev Oral Biol Med doi: 10.1177/154411130201300302 – year: 2018 ident: CR16 article-title: O-GlcNAc: a novel regulator of immunometabolism publication-title: J Bioenerg Biomembr doi: 10.1007/s10863-018-9744-1 – year: 2013 ident: CR46 article-title: O-GlcNAc transferase inhibitsLPS-mediated expression of inducible nitric oxide synthase through an increased interaction with mSin3A in RAW264.7 cells publication-title: Am J Physiol Cell Physiol. doi: 10.1152/ajpcell.00042.2013 – year: 2011 ident: CR80 article-title: Pseudomonas aeruginosa enhances production of an antimicrobial in response to -acetylglucosamine and peptidoglycan publication-title: J Bacteriol doi: 10.1128/JB.01175-10 – year: 2013 ident: CR34 article-title: Activation of the transcriptional function of the NF-κB protein c-Rel by -GlcNAc glycosylation publication-title: Sci Signal. doi: 10.1126/scisignal.20040 – year: 2004 ident: CR59 article-title: Neutrophils exhibit rapid agonist-induced increases in protein-associated -GlcNAc publication-title: J Biol Chem doi: 10.1074/jbc.M407911200 – year: 2004 ident: CR88 article-title: Integrated regulatory responses of fimB to -acetylneuraminic (sialic) acid and GlcNAc in K-12 publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.0405821101 – year: 2023 ident: CR78 article-title: Glutamine promotes O-GlcNAcylation of G6PD and inhibits AGR2 -glutathionylation to maintain the intestinal mucus barrier in burned septic mice publication-title: Redox Biol doi: 10.1016/j.redox.2022.102581 – year: 2019 ident: 48_CR8 publication-title: Sci Rep doi: 10.1038/s41598-019-55381-7 – year: 2023 ident: 48_CR83 publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.2119658120 – year: 2009 ident: 48_CR3 publication-title: Nat Med doi: 10.1038/nm0509-496 – year: 2020 ident: 48_CR11 publication-title: Nat Immunol doi: 10.1038/s41590-020-0789-z – year: 2016 ident: 48_CR29 publication-title: Nat Immunol doi: 10.1038/ni.3439 – year: 2018 ident: 48_CR31 publication-title: FEBS J doi: 10.1111/febs.14491 – year: 2016 ident: 48_CR17 publication-title: Am J Crit Care doi: 10.4037/ajcc2016432 – year: 2020 ident: 48_CR53 publication-title: Eur J Pharmacol doi: 10.1016/j.ejphar.2020.173090 – year: 2017 ident: 48_CR48 publication-title: J Cereb Blood Flow Metab doi: 10.1177/0271678X16679671 – year: 2021 ident: 48_CR24 publication-title: Physiol Rev doi: 10.1152/physrev.00043.2019 – year: 2017 ident: 48_CR36 publication-title: J Immunol doi: 10.4049/jimmunol.1601727 – year: 2018 ident: 48_CR69 publication-title: Nat Commun doi: 10.1038/s41467-018-04719-2 – year: 2003 ident: 48_CR14 publication-title: Shock doi: 10.1097/01.shk.0000068322.08268.b4 – year: 2017 ident: 48_CR41 publication-title: ACS Chem Biol doi: 10.1021/acschembio.7b00869 – year: 2004 ident: 48_CR88 publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.0405821101 – year: 2021 ident: 48_CR54 publication-title: Int Immunopharmacol doi: 10.1016/j.intimp.2021.107791 – year: 2019 ident: 48_CR37 publication-title: J Biol Chem doi: 10.1074/jbc.RA119.008373 – year: 2006 ident: 48_CR89 publication-title: J Bacteriol doi: 10.1128/JB.00234-06 – year: 2007 ident: 48_CR32 publication-title: EMBO J doi: 10.1038/sj.emboj.7601845 – year: 2013 ident: 48_CR85 publication-title: PLoS Pathog doi: 10.1371/journal.ppat.1003080 – year: 2016 ident: 48_CR44 publication-title: Nat Commun doi: 10.1038/ncomms12526 – year: 2022 ident: 48_CR70 publication-title: Front Immunol doi: 10.3389/fimmu.2022.841299 – year: 2019 ident: 48_CR74 publication-title: Sci Rep doi: 10.1038/s41598-019-55381-7 – year: 2019 ident: 48_CR75 publication-title: Front Physiol doi: 10.3389/fphys.2019.01614 – year: 2013 ident: 48_CR42 publication-title: J Allergy Clin Immunol doi: 10.1016/j.jaci.2013.01.046 – year: 2016 ident: 48_CR57 publication-title: Front Immunol doi: 10.3389/fimmu.2016.00155 – year: 2002 ident: 48_CR62 publication-title: Crit Rev Oral Biol Med doi: 10.1177/154411130201300302 – year: 2015 ident: 48_CR66 publication-title: Proc Natl Acad Sci US A doi: 10.1073/pnas.1521740112 – year: 2016 ident: 48_CR1 publication-title: JAMA doi: 10.1001/jama.2016.0287 – year: 2019 ident: 48_CR51 publication-title: Nat Rev Cancer doi: 10.1038/s41568-018-0090-8 – year: 2019 ident: 48_CR50 publication-title: Immunity doi: 10.1016/j.immuni.2019.01.007 – volume: 4 start-page: 07 year: 2016 ident: 48_CR13 publication-title: Cell. – year: 2018 ident: 48_CR16 publication-title: J Bioenerg Biomembr doi: 10.1007/s10863-018-9744-1 – year: 2008 ident: 48_CR58 publication-title: Cytometry A doi: 10.1002/cyto.a.20569 – year: 2022 ident: 48_CR2 publication-title: Annu Rev Physiol doi: 10.1146/annurev-physiol-061121-040214 – year: 2008 ident: 48_CR72 publication-title: J Immunol doi: 10.4049/jimmunol.181.8.5481 – year: 2017 ident: 48_CR33 publication-title: J Biol Chem doi: 10.1074/jbcM116.766568 – year: 2014 ident: 48_CR30 publication-title: J Immunol doi: 10.4049/jimmunol.1302259 – year: 2022 ident: 48_CR79 publication-title: Int J Mol Sci doi: 10.3390/ijms23126430 – year: 2013 ident: 48_CR34 publication-title: Sci Signal. doi: 10.1126/scisignal.20040 – year: 2002 ident: 48_CR64 publication-title: Immunity doi: 10.1016/s1074-7613(02)00333-3 – year: 2021 ident: 48_CR4 publication-title: Front Immunol doi: 10.3389/fimmu.2021.701675 – year: 2022 ident: 48_CR22 publication-title: Front Endocrinol (Lausanne) doi: 10.3389/fendo.2022.943576 – year: 2017 ident: 48_CR25 publication-title: Nat Rev Mol Cell Biol doi: 10.1038/nrm.2017.22 – year: 2005 ident: 48_CR61 publication-title: J Biol Chem doi: 10.1074/jbc.M414066200 – year: 2019 ident: 48_CR65 publication-title: Oncogene doi: 10.1038/s41388-018-0435-5 – year: 2022 ident: 48_CR27 publication-title: Metabolites doi: 10.3390/metabo12080725 – year: 2017 ident: 48_CR12 publication-title: Front Cell Infect Microbiol doi: 10.3389/fcimb.2017.00373 – year: 2020 ident: 48_CR28 publication-title: Neuromo-lecular Med doi: 10.1007/s12017-019-08584-0 – year: 2013 ident: 48_CR47 publication-title: Br J Pharmacol doi: 10.1111/bph.12223 – year: 2015 ident: 48_CR56 publication-title: Cardiovasc Hematol Disord Drug Targets doi: 10.2174/1871529x15666150108113236 – year: 2017 ident: 48_CR45 publication-title: Crit Care Med doi: 10.1097/CCM.0000000000002380 – year: 2022 ident: 48_CR7 publication-title: Int J Mol Sci doi: 10.3390/ijms231911260 – year: 2019 ident: 48_CR38 publication-title: Nat Commun doi: 10.1038/s41467-019-08300-3 – year: 2014 ident: 48_CR10 publication-title: Virulence doi: 10.4161/viru.26516 – year: 2021 ident: 48_CR77 publication-title: NeuroReport doi: 10.1097/WNR.0000000000001582 – year: 2021 ident: 48_CR5 publication-title: Cells doi: 10.3390/cells10112962 – year: 2015 ident: 48_CR86 publication-title: PLoS Pathog doi: 10.1371/journal.ppat.1004701 – year: 2013 ident: 48_CR46 publication-title: Am J Physiol Cell Physiol. doi: 10.1152/ajpcell.00042.2013 – year: 2005 ident: 48_CR18 publication-title: Clin Immunol doi: 10.1016/j.clim.2004.08.015 – year: 2009 ident: 48_CR39 publication-title: Annu Rev Immunol doi: 10.1146/annurev.Immunol.021908.132706 – year: 2020 ident: 48_CR20 publication-title: Int J Mol Sci doi: 10.3390/ijms21072356 – year: 2004 ident: 48_CR59 publication-title: J Biol Chem doi: 10.1074/jbc.M407911200 – volume: 259 start-page: 3308 issue: 5 year: 1984 ident: 48_CR21 publication-title: J Biol Chem. doi: 10.1016/S0021-9258(17)43295-9 – year: 2021 ident: 48_CR26 publication-title: Cancers (Basel) doi: 10.3390/cancers13071666 – year: 2019 ident: 48_CR55 publication-title: J Biol Chem doi: 10.1074/jbc.RA118.004638 – year: 2019 ident: 48_CR9 publication-title: Curr Protein Pept Sci doi: 10.2174/1389203720666190305164128 – year: 2017 ident: 48_CR49 publication-title: J Biol Chem doi: 10.1074/jbc.M116.737940 – year: 2018 ident: 48_CR71 publication-title: Immunology doi: 10.1111/imm.12854 – year: 2016 ident: 48_CR73 publication-title: Cell. doi: 10.1016/j.cell.2016.05.056 – year: 2021 ident: 48_CR76 publication-title: Int J Mol Sci doi: 10.3390/ijms22179236 – year: 2010 ident: 48_CR15 publication-title: J Immunol doi: 10.4049/jimmunol.0903151 – year: 2018 ident: 48_CR68 publication-title: Natl Acad Sci USA doi: 10.1073/pnas.1801850115 – year: 2019 ident: 48_CR6 publication-title: Genome Med doi: 10.1186/s13073-019-0674-2 – year: 2014 ident: 48_CR82 publication-title: Cell Microbiol doi: 10.1111/cmi.12304 – year: 2021 ident: 48_CR60 publication-title: Biomed Pharmacother. doi: 10.1016/j.biopha.2021.111477 – year: 2017 ident: 48_CR84 publication-title: Mol Microbiol doi: 10.1111/mmi.13849 – year: 2017 ident: 48_CR52 publication-title: J Exp Med doi: 10.1084/jem.20161105 – year: 2016 ident: 48_CR19 publication-title: Inflamm Res doi: 10.1007/s00011-016-0970-x – year: 2005 ident: 48_CR40 publication-title: J Immunol doi: 10.4049/jimmunol.175.12.8003 – year: 2014 ident: 48_CR67 publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.1323226111 – year: 2018 ident: 48_CR23 publication-title: J Bioenerg 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Snippet | O-GlcNAc modification is a glycosylation modification that is commonly observed in nuclear and organelle proteins of cells. In recent years, several studies... Abstract O-GlcNAc modification is a glycosylation modification that is commonly observed in nuclear and organelle proteins of cells. In recent years, several... |
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SubjectTerms | Immune cells Inflammation Medicine Medicine & Public Health O-GlcNAcylation modification Review Article Sepsis |
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