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      KCI등재 SCI SCIE SCOPUS

      The Role of High Mobility Group Box 1 in Innate Immunity

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      https://www.riss.kr/link?id=A101616796

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      다국어 초록 (Multilingual Abstract)

      With growing accounts of inflammatory diseases such as sepsis, greater understandingthe immune system and the mechanisms of cellular immunity have become primaryobjectives in immunology studies. High mobility group box 1 (HMGB1) is a ubiquitous nuclea...

      With growing accounts of inflammatory diseases such as sepsis, greater understandingthe immune system and the mechanisms of cellular immunity have become primaryobjectives in immunology studies. High mobility group box 1 (HMGB1) is a ubiquitous nuclear protein that is implicated in various aspects of the innate immune system as a damage-associated molecular pattern molecule and a late mediator of inflammation, as well as in principal cellular processes, such as autophagy and apoptosis. HMGB1 functions in the nucleus as a DNA chaperone; however, it exhibits cytokine-like activity when secreted by injurious or infectious stimuli. Extracellular HMGB1 acts through specific receptors to promote activation of the NF-κB signalingpathway, leading to production of cytokines and chemokines. These findings furtherimplicate HMGB1 in lethal inflammatory diseases as a crucial regulator of inflammatory,injurious, and infectious responses. In this paper, we summarize the role of HMGB1 in inflammatory and non-inflammatory states and assess potential therapeuticapproaches targeting HMGB1 in inflammatory diseases.

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      참고문헌 (Reference)

      1 Kissoon N, "World Federation of Pediatric Intensive Care and Critical Care Societies: Global Sepsis Initiative" 12 : 494-503, 2011

      2 Poser I, "Upregulation of HMG1 leads to melanoma inhibitory activity expression in malignant melanoma cells and contributes to their malignancy phenotype" 23 : 2991-2998, 2003

      3 van Beijnum JR, "Tumor angiogenesis is enforced by autocrine regulation of high-mobility group box 1" 32 : 363-374, 2013

      4 Tian J, "Toll-like receptor 9-dependent activation by DNA-containing immune complexes is mediated by HMGB1 and RAGE" 8 : 487-496, 2007

      5 Park BS, "The structural basis of lipopolysaccharide recognition by the TLR4-MD-2 complex" NATURE PUBLISHING GROUP 458 (458): 1191-1195, 2009

      6 Hori O, "The receptor for advanced glycation end products (RAGE) is a cellular binding site for amphoterin. Mediation of neurite outgrowth and co-expression of rage and amphoterin in the developing nervous system" 270 : 25752-25761, 1995

      7 Gardella S, "The nuclear protein HMGB1 is secreted by monocytes via a non-classical, vesicle-mediated secretory pathway" 3 : 995-1001, 2002

      8 Paull TT, "The nonspecific DNA-binding and -bending proteins HMG1 and HMG2 promote the assembly of complex nucleoprotein structures" 7 : 1521-1534, 1993

      9 Conti L, "The noninflammatory role of high mobility group box 1/Toll-like receptor 2 axis in the self-renewal of mammary cancer stem cells" 27 : 4731-4744, 2013

      10 Knapp S, "The long acidic tail of high mobility group box 1 (HMGB1) protein forms an extended and flexible structure that interacts with specific residues within and between the HMG boxes" 43 : 11992-11997, 2004

      1 Kissoon N, "World Federation of Pediatric Intensive Care and Critical Care Societies: Global Sepsis Initiative" 12 : 494-503, 2011

      2 Poser I, "Upregulation of HMG1 leads to melanoma inhibitory activity expression in malignant melanoma cells and contributes to their malignancy phenotype" 23 : 2991-2998, 2003

      3 van Beijnum JR, "Tumor angiogenesis is enforced by autocrine regulation of high-mobility group box 1" 32 : 363-374, 2013

      4 Tian J, "Toll-like receptor 9-dependent activation by DNA-containing immune complexes is mediated by HMGB1 and RAGE" 8 : 487-496, 2007

      5 Park BS, "The structural basis of lipopolysaccharide recognition by the TLR4-MD-2 complex" NATURE PUBLISHING GROUP 458 (458): 1191-1195, 2009

      6 Hori O, "The receptor for advanced glycation end products (RAGE) is a cellular binding site for amphoterin. Mediation of neurite outgrowth and co-expression of rage and amphoterin in the developing nervous system" 270 : 25752-25761, 1995

      7 Gardella S, "The nuclear protein HMGB1 is secreted by monocytes via a non-classical, vesicle-mediated secretory pathway" 3 : 995-1001, 2002

      8 Paull TT, "The nonspecific DNA-binding and -bending proteins HMG1 and HMG2 promote the assembly of complex nucleoprotein structures" 7 : 1521-1534, 1993

      9 Conti L, "The noninflammatory role of high mobility group box 1/Toll-like receptor 2 axis in the self-renewal of mammary cancer stem cells" 27 : 4731-4744, 2013

      10 Knapp S, "The long acidic tail of high mobility group box 1 (HMGB1) protein forms an extended and flexible structure that interacts with specific residues within and between the HMG boxes" 43 : 11992-11997, 2004

      11 Calogero S, "The lack of chromosomal protein Hmg1 does not disrupt cell growth but causes lethal hypoglycaemia in newborn mice" 22 : 276-280, 1999

      12 Goodwin GH, "The isolation of the high mobility group non-histone chromosomal protein HMG 14" 80 : 413-416, 1977

      13 Mitkova E, "The inhibitory effect of HMGB-1 protein on the repair of cisplatin-damaged DNA is accomplished through the acidic domain" 44 : 5893-5898, 2005

      14 Bell CW, "The extracellular release of HMGB1 during apoptotic cell death" 291 : C1318-C1325, 2006

      15 Giese K, "The HMG domain of lymphoid enhancer factor 1 bends DNA and facilitates assembly of functional nucleoprotein structures" 69 : 185-195, 1992

      16 Latz E, "TLR9 signals after translocating from the ER to CpG DNA in the lysosome" 5 : 190-198, 2004

      17 Levy RM, "Systemic inflammation and remote organ injury following trauma require HMGB1" 293 : R1538-R1544, 2007

      18 Weir HM, "Structure of the HMG box motif in the B-domain of HMG1" 12 : 1311-1319, 1993

      19 Li J, "Structural basis for the proinflammatory cytokine activity of high mobility group box 1" 9 : 37-45, 2003

      20 Chen GY, "Sterile inflammation: sensing and reacting to damage" 10 : 826-837, 2010

      21 Taniguchi N, "Stage-specific secretion of HMGB1 in cartilage regulates endochondral ossification" 27 : 5650-5663, 2007

      22 Bianchi ME, "Specific recognition of cruciform DNA by nuclear protein HMG1" 243 (243): 1056-1059, 1989

      23 Kim S, "Signaling of high mobility group box 1 (HMGB1) through toll-like receptor 4 in macrophages requires CD14" 19 : 88-98, 2013

      24 Tye H, "STAT3-driven upregulation of TLR2 promotes gastric tumorigenesis independent of tumor inflammation" 22 : 466-478, 2012

      25 Belgrano FS, "Role of the acidic tail of high mobility group protein B1 (HMGB1) in protein stability and DNA bending" 8 : e79572-, 2013

      26 Qin S, "Role of HMGB1 in apoptosis-mediated sepsis lethality" 203 : 1637-1642, 2006

      27 Bustin M, "Revised nomenclature for high mobility group (HMG) chromosomal proteins" 26 : 152-153, 2001

      28 Yang H, "Reversing established sepsis with antagonists of endogenous high-mobility group box 1" 101 : 296-301, 2004

      29 Campana L, "Requirement of HMGB1 for stromal cell-derived factor-1/CXCL12-dependent migration of macrophages and dendritic cells" 86 : 609-615, 2009

      30 Dumitriu IE, "Release of high mobility group box 1 by dendritic cells controls T cell activation via the receptor for advanced glycation end products" 174 : 7506-7515, 2005

      31 Scaffidi P, "Release of chromatin protein HMGB1 by necrotic cells triggers inflammation" 418 : 191-195, 2002

      32 Korkaya H, "Regulation of cancer stem cells by cytokine networks: attacking cancer’s inflammatory roots" 17 : 6125-6129, 2011

      33 Yang H, "Redox modification of cysteine residues regulates the cytokine activity of high mobility group box-1 (HMGB1)" 18 : 250-259, 2012

      34 Huttunen HJ, "Receptor for advanced glycation end products (RAGE)-mediated neurite outgrowth and activation of NF-kappaB require the cytoplasmic domain of the receptor but different downstream signaling pathways" 274 : 19919-19924, 1999

      35 Kokkola R, "RAGE is the major receptor for the proinflammatory activity of HMGB1 in rodent macrophages" 61 : 1-9, 2005

      36 Ito T, "Proteolytic cleavage of high mobility group box 1 protein by thrombin-thrombomodulin complexes" 28 : 1825-1830, 2008

      37 Robert SM, "Preconditioning with high mobility group box 1 (HMGB1) induces lipoteichoic acid (LTA) tolerance" 33 : 663-671, 2010

      38 Aneja RK, "Preconditioning with high mobility group box 1 (HMGB1) induces lipopolysaccharide (LPS) tolerance" 84 : 1326-1334, 2008

      39 Ito I, "Post-translational methylation of high mobility group box 1 (HMGB1) causes its cytoplasmic localization in neutrophils" 282 : 16336-16344, 2007

      40 Youn JH, "Nucleocytoplasmic shuttling of HMGB1 is regulated by phosphorylation that redirects it toward secretion" 177 (177): 7889-7897, 2006

      41 Javaherian K, "Nonhistone proteins HMG1 and HMG2 change the DNA helical structure" 199 : 1345-1346, 1978

      42 Semino C, "NK/iDC interaction results in IL-18 secretion by DCs at the synaptic cleft followed by NK cell activation and release of the DC maturation factor HMGB1" 106 : 609-616, 2005

      43 Srikrishna G, "N -Glycans on the receptor for advanced glycation end products influence amphoterin binding and neurite outgrowth" 80 : 998-1008, 2002

      44 Venereau E, "Mutually exclusive redox forms of HMGB1 promote cell recruitment or proinflammatory cytokine release" 209 : 1519-1528, 2012

      45 Bonaldi T, "Monocytic cells hyperacetylate chromatin protein HMGB1 to redirect it towards secretion" 22 : 5551-5560, 2003

      46 Hoppe G, "Molecular basis for the redox control of nuclear transport of the structural chromatin protein Hmgb1" 312 : 3526-3538, 2006

      47 Kang R, "Metabolic regulation by HMGB1-mediated autophagy and mitophagy" 7 : 1256-1258, 2011

      48 Ellerman JE, "Masquerader: high mobility group box-1 and cancer" 13 : 2836-2848, 2007

      49 Watson M, "Mapping intramolecular interactions between domains in HMGB1 using a tail-truncation approach" 374 : 1286-1297, 2007

      50 Schröder NW, "Lipoteichoic acid (LTA) of Streptococcus pneumoniae and Staphylococcus aureus activates immune cells via Toll-like receptor (TLR)-2, lipopolysaccharide-binding protein (LBP), and CD14, whereas TLR-4 and MD-2 are not involved" 278 : 15587-15594, 2003

      51 Saitoh S, "Ligand-dependent Toll-like receptor 4 (TLR4)-oligomerization is directly linked with TLR4-signaling" 10 : 257-260, 2004

      52 Urbonaviciute V, "Induction of inflammatory and immune responses by HMGB1-nucleosome complexes: implications for the pathogenesis of SLE" 205 : 3007-3018, 2008

      53 Kazama H, "Induction of immunological tolerance by apoptotic cells requires caspase-dependent oxidation of high-mobility group box-1 protein" 29 : 21-32, 2008

      54 Choi J, "Increased levels of HMGB1 and pro-inflammatory cytokines in children with febrile seizures" BIOMED CENTRAL LTD 8 : 135-, 2011

      55 Popovic K, "Increased expression of the novel proinflammatory cytokine high mobility group box chromosomal protein 1 in skin lesions of patients with lupus erythematosus" 52 : 3639-3645, 2005

      56 Youn JH, "Identification of lipopolysaccharide-binding peptide regions within HMGB1 and their effects on subclinical endotoxemia in a mouse model" WILEY-V C H VERLAG GMBH 41 (41): 2753-2762, 2011

      57 Lin Q, "High-mobility group box-1 mediates toll-like receptor 4-dependent angiogenesis" 31 : 1024-1032, 2011

      58 Straino S, "High-mobility group box 1 protein in human and murine skin: involvement in wound healing" 128 : 1545-1553, 2008

      59 Huebener P, "High-mobility group box 1 is dispensable for autophagy, mitochondrial quality control, and organ function in vivo" 19 : 539-547, 2014

      60 Yang D, "High mobility group box-1 protein induces the migration and activation of human dendritic cells and acts as an alarmin" 81 : 59-66, 2007

      61 Messmer D, "High mobility group box protein 1: an endogenous signal for dendritic cell maturation and Th1 polarization" 173 : 307-313, 2004

      62 Taniguchi N, "High mobility group box chromosomal protein 1 plays a role in the pathogenesis of rheumatoid arthritis as a novel cytokine" 48 : 971-981, 2003

      63 Dong Xda E, "High mobility group box I (HMGB1) release from tumor cells after treatment: implications for development of targeted chemoimmunotherapy" 30 : 596-606, 2007

      64 Youn JH, "High mobility group box 1 protein binding to lipopolysaccharide facilitates transfer of lipopolysaccharide to CD14 and enhances lipopolysaccharide-mediated TNF-alpha production in human monocytes" 180 : 5067-5074, 2008

      65 Falciola L, "High mobility group 1 protein is not stably associated with the chromosomes of somatic cells" 137 : 19-26, 1997

      66 Andersson U, "High mobility group 1 protein (HMG-1) stimulates proinflammatory cytokine synthesis in human monocytes" 192 : 565-570, 2000

      67 Kang R, "HMGB1: a novel Beclin 1-binding protein active in autophagy" 6 : 1209-1211, 2010

      68 Tang D, "HMGB1 release and redox regulates autophagy and apoptosis in cancer cells" 29 : 5299-5310, 2010

      69 Schiraldi M, "HMGB1 promotes recruitment of inflammatory cells to damaged tissues by forming a complex with CXCL12 and signaling via CXCR4" 209 : 551-563, 2012

      70 Rovere-Querini P, "HMGB1 is an endogenous immune adjuvant released by necrotic cells" 5 : 825-830, 2004

      71 Brezniceanu ML, "HMGB1 inhibits cell death in yeast and mammalian cells and is abundantly expressed in human breast carcinoma" 17 : 1295-1297, 2003

      72 Sha Y, "HMGB1 develops enhanced proinflammatory activity by binding to cytokines" 180 : 2531-2537, 2008

      73 Bassi R, "HMGB1 as an autocrine stimulus in human T98G glioblastoma cells: role in cell growth and migration" 87 : 23-33, 2008

      74 Oh YJ, "HMGB1 Is Phosphorylated by Classical Protein Kinase C and Is Secreted by a Calcium-Dependent Mechanism" AMER ASSOC IMMUNOLOGISTS 182 : 5800-5809, 2009

      75 Stros M, "HMGB proteins: interactions with DNA and chromatin" 1799 : 101-113, 2010

      76 Sparatore B, "Extracellular high-mobility group 1 protein is essential for murine erythroleukaemia cell differentiation" 320 (320): 253-256, 1996

      77 Tang D, "Endogenous HMGB1 regulates autophagy" 190 : 881-892, 2010

      78 Goldstein RS, "Elevated high-mobility group box 1 levels in patients with cerebral and myocardial ischemia" 25 : 571-574, 2006

      79 Antoine DJ, "Diet restriction inhibits apoptosis and HMGB1 oxidation and promotes inflammatory cell recruitment during acetaminophen hepatotoxicity" 16 : 479-490, 2010

      80 Ganz T, "Defensins: antimicrobial peptides of innate immunity" 3 : 710-720, 2003

      81 Mitola S, "Cutting edge: extracellular high mobility group box-1 protein is a proangiogenic cytokine" 176 : 12-15, 2006

      82 Yanai H, "Conditional ablation of HMGB1 in mice reveals its protective function against endotoxemia and bacterial infection" 110 : 20699-20704, 2013

      83 Wang H, "Che J, et al. HMG-1 as a late mediator of endotoxin lethality in mice" 285 : 248-251, 1999

      84 Mbitikon-Kobo FM, "Characterization of a CD44/CD122int memory CD8 T cell subset generated under sterile inflammatory conditions" 182 : 3846-3854, 2009

      85 Min HJ, "Chaperone-like Activity of High-Mobility Group Box 1 Protein and Its Role in Reducing the Formation of Polyglutamine Aggregates" AMER ASSOC IMMUNOLOGISTS 190 (190): 1797-1806, 2013

      86 Teicher BA, "CXCL12 (SDF-1)/CXCR4 pathway in cancer" 16 : 2927-2931, 2010

      87 Oh YJ, "CKD712, (S)-1-(α-naphthylmethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline, inhibits the lipopolysaccharide-stimulated secretion of HMGB1 by inhibiting PI3K and classical protein kinase C" 11 : 1160-1165, 2011

      88 Taguchi A, "Blockade of RAGE-amphoterin signalling suppresses tumour growth and metastases" 405 : 354-360, 2000

      89 Liu Z, "Blockade of Autocrine TGF-β Signaling Inhibits Stem Cell Phenotype, Survival, and Metastasis of Murine Breast Cancer Cells" 2 : 1-8, 2012

      90 Yang D, "Antimicrobial proteins act as “alarmins” in joint immune defense" 50 : 3401-3403, 2004

      91 Schlueter C, "Angiogenetic signaling through hypoxia: HMGB1: an angiogenetic switch molecule" 166 : 1259-1263, 2005

      92 Laudet V, "Ancestry and diversity of the HMG box superfamily" 21 : 2493-2501, 1993

      93 Oppenheim JJ, "Alarmins: chemotactic activators of immune responses" 17 : 359-365, 2005

      94 Park JS, "Activation of gene expression in human neutrophils by high mobility group box 1 protein" 284 : C870-C879, 2003

      95 Ivanov S, "A novel role for HMGB1 in TLR9-mediated inflammatory responses to CpG-DNA" 110 : 1970-1981, 2007

      96 Goodwin GH, "A new group of chromatin-associated proteins with a high content of acidic and basic amino acids" 38 : 14-19, 1973

      97 Li W, "A major ingredient of green tea rescues mice from lethal sepsis partly by inhibiting HMGB1" 2 : e1153-, 2007

      98 Yang H, "A critical cysteine is required for HMGB1 binding to Toll-like receptor 4 and activation of macrophage cytokine release" 107 : 11942-11947, 2010

      99 Tang D, "A Janus tale of two active high mobility group box 1 (HMGB1) redox states" 18 : 1360-1362, 2012

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