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Receptor-Dependent Mechanisms of Cell Stimulation by Bacterial Endotoxin
Abstract
In humans and experimental animals the presence of bacterial lipopolysaccharide (endotoxin, LPS) signals the presence of gram-negative bacteria. Recognition of LPS triggers gene induction by myeloid and nonmyeloid lineage cells. These inducible genes encode proteins that include cytokines, adhesive proteins, and enzymes that produce low molecular weight proinflammatory mediators. Together the products of these inducible genes upregulate host defense systems that participate in eliminating the bacterial infection. Unfortunately, these same mediators contribute to a serious human disease known as septic shock. Considerable progress has been made during the past decade in determining the sources, identities, and sequence of release of these mediators. In contrast, until recently, marked gaps in our knowledge existed regarding the identity of the LPS receptor and intracellular signaling pathways responsible for LPS-induced cell activation. The discovery in 1986 of a plasma protein termed LPS binding protein (LBP) led to the discovery of unanticipated mechanisms of LPS-induced cell activation. CD14 was found as a soluble serum protein or as a glycosylphosphatidylinositol (GPI)-anchored protein of myeloid lineage cells; it now occupies a key role in LPS-induced cell activation as we understand it today. Here we discuss how LBP enables LPS binding to CD14 and how complexes of LPS and soluble or GPI-anchored CD14 participate in cell activation. We also review the evidence supporting a model for a functional LPS receptor of myeloid cells, which is multimeric, comprised of GPI-anchored CD14 and a presently unidentified transmembrane protein that together bind LPS and initiate cell activation via kinase cascades.
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“bacterial cell wall lipopolysaccharides (LPS) induce synthesis of IL-18.20”
From The Gut Microbiome and the Brain (2014) · cites this paper as [20]
Citations
Cites
A MAP Kinase Targeted by Endotoxin and Hyperosmolarity in Mammalian Cells
Han, J., Lee, J. D., Bibbs, L., & Ulevitch, R. J. (1994) · Science · doi:10.1126/science.7914033 · Cited by 2,647
Self-citationStructure and Function of Lipopolysaccharide Binding Protein
Schumann, R. R., Leong, S. R., Flaggs, G., Gray, P. W., Wright, S. D., Mathison, J. C., Tobias, P. S., & Ulevitch, R. J. (1990) · Science · doi:10.1126/science.2402637 · Cited by 1,672
Self-citationThe immune system evolved to discriminate infectious nonself from noninfectious self
Janeway, C. A. (1992) · Immunology Today · doi:10.1016/0167-5699(92)90198-g · Cited by 1,343
Takeda, J., Miyata, T., Kawagoe, K., Iida, Y., Endo, Y., Fujita, T., Takahashi, M., Kitani, T., & Kinoshita, T. (1993) · Cell · doi:10.1016/0092-8674(93)90250-t · Cited by 1,059
A Divergence in the MAP Kinase Regulatory Network Defined by MEK Kinase and Raf
Lange-Carter, C. A., Pleiman, C. M., Gardner, A. M., Blumer, K. J., & Johnson, G. L. (1993) · Science · doi:10.1126/science.8385802 · Cited by 827
Potocytosis: Sequestration and Transport of Small Molecules by Caveolae
Anderson, R. G. W., Kamen, B. A., Rothberg, K. G., & Lacey, S. W. (1992) · Science · doi:10.1126/science.1310359 · Cited by 734
Haziot, A., Chen, S., Ferrero, E., Low, M. G., Silber, R., & Goyert, S. M. (1988) · The Journal of Immunology · doi:10.4049/jimmunol.141.2.547 · Cited by 645
Atomic structure of the MAP kinase ERK2 at 2.3 A resolution
Zhang, F., Strand, A., Robbins, D., Cobb, M. H., & Goldsmith, E. J. (1994) · Nature · doi:10.1038/367704a0 · Cited by 592
Isolation of a lipopolysaccharide-binding acute phase reactant from rabbit serum.
Tobias, P. S., Soldau, K., & Ulevitch, R. J. (1986) · The Journal of Experimental Medicine · doi:10.1084/jem.164.3.777 · Cited by 547
Self-citationRaetz, C. R. H., Ulevitch, R. I., Wright, S. D., Sibley, C. H., Ding, A. H., & Nathan, C. (1991) · The FASEB Journal · doi:10.1096/fasebj.5.12.1916089 · Cited by 507
Self-citation
Cited by
Sorted by citations
Items 101–200 of 1,000
Su, G. L., Klein, R., Aminlari, A., Zhang, H. Y., Steinstraesser, L., Alarcon, W. H., Remick, D., & Wang, S. C. (2000) · Hepatology · doi:10.1053/he.2000.5634 · Cited by 280
Scott, M. G., Vreugdenhil, A. C. E., Buurman, W. A., Hancock, R. E. W., & Gold, M. R. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.2.549 · Cited by 270
Cellular Events Mediated by Lipopolysaccharide-stimulated Toll-like Receptor 4
Yang, H., Young, D. W., Gusovsky, F., & Chow, J. C. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m002896200 · Cited by 267
Guerra-Ruiz, A. R., Casafont, F., Crespo, J., Cayón, A., Mayorga, M. M., Estébanez, Á., Fernández-Escalante, J. C., & Pons‐Romero, F. (2007) · Obesity Surgery · doi:10.1007/s11695-007-9243-7 · Cited by 268
Holloway, J. W., Yang, I. A., & Holgate, S. T. (2010) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2009.10.071 · Cited by 280
Requirement for STAT1 in LPS-induced gene expression in macrophages
Ohmori, Y., & Hamilton, T. A. (2001) · Journal of Leukocyte Biology · doi:10.1189/jlb.69.4.598 · Cited by 267
“Lipopolysaccharide (LPS), a component of bacterial cell walls, is a potent macrophage-activating stimulus which induces expression of many genes necessary for the execution of host defense function [2–4].”
BackgroundCytokine signaling-regulation of the immune response in normal and critically ill states
Oberholzer, A., Oberholzer, C., & Moldawer, L. L. (2000) · Critical Care Medicine · doi:10.1097/00003246-200004001-00002 · Cited by 266
“However, the innate immune system can also rely on the recognition of other "pathogen-specific" entities, such as CpG motifs unique to bacterial DNA (4, 5) and soluble glycoconjugates that are recognized by macrophages (6).”
BackgroundHoffmann, A., Kann, O., Ohlemeyer, C., Hanisch, U., & Kettenmann, H. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-11-04410.2003 · Cited by 263
“LPS triggers activation of macrophage-like cells and is used as a tool to mimic Gramnegative infection (abd-el-Basset and Fedoroff, 1995; Ulevitch and Tobias, 1995).”
BackgroundMethodRole of CD14 in host protection against infections and in metabolism regulation
Zanoni, I., & Granucci, F. (2013) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2013.00032 · Cited by 262
“CD14 is a 55 kDa glycoprotein expressed on the surface of myelomonocytic cells as a glycosylphosphatidylinositol (GPI)anchored receptor or can be secreted in a soluble form (Ulevitch and Tobias, 1995).”
BackgroundMethodInfluentialMD-2 and TLR4 N-Linked Glycosylations Are Important for a Functional Lipopolysaccharide Receptor
Correia, J. D. S., & Ulevitch, R. J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m109910200 · Cited by 262
Self-citationvan Vliet, E. A., Aronica, E., Vezzani, A., & Ravizza, T. (2017) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12444 · Cited by 267
Adamo, R., Sokol, S., Soong, G., Gómez, M. I., & Prince, A. S. (2003) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2003-0260oc · Cited by 258
“Mucosal responses to bacteria depend upon the expression of ligand-specific TLRs and essential coreceptors at the site of infection ( 8 , 9). Unlike nonpolarized cells of hematopoetic origin, the distribution of TLRs in polarized mucosal cells may be important in facilitating their surveillance function.”
BackgroundMartin, M., Schifferle, R. E., Cuesta, N., Vogel, S. N., Katz, J., & Michalek, S. M. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.2.717 · Cited by 265
“sponses, as well as contribute to endotoxin shock (14, 15, 21, 22).”
BackgroundOpal, S. M., & Cohen, J. (1999) · Critical Care Medicine · doi:10.1097/00003246-199908000-00039 · Cited by 258
The Relationship Between Gut Microbiota and Inflammatory Diseases: The Role of Macrophages
Wang, J., Chen, W., & Wang, Y. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01065 · Cited by 269
Toll-Like Receptors: General Molecular and Structural Biology
Behzadi, P., García‐Perdomo, H. A., & Karpiński, T. M. M. (2021) · Journal of Immunology Research · doi:10.1155/2021/9914854 · Cited by 267
Microbes, immunity, and behavior: psychoneuroimmunology meets the microbiome
Dinan, T. G., & Cryan, J. F. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2016.103 · Cited by 246
Dual Roles for Perivascular Macrophages in Immune-to-Brain Signaling
Serrats, J., Schiltz, J. C., García-Bueno, B., van Rooijen, N., Reyes, T. M., & Sawchenko, P. E. (2010) · Neuron · doi:10.1016/j.neuron.2009.11.032 · Cited by 253
Wang, P., & Ohura, K. (2002) · Critical Reviews in Oral Biology and Medicine · doi:10.1177/154411130201300204 · Cited by 278
Immunostimulatory DNA: Sequence‐dependent production of potentially harmful or useful cytokines
Lipford, G. B., Sparwasser, T. D., Bauer, M., Zimmermann, S., Koch, E. S., Heeg, K. M., & Wagner, H. (1997) · European Journal of Immunology · doi:10.1002/eji.1830271242 · Cited by 249
Bhat, N. R., & Zhang, P. (1999) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1999.0720112.x · Cited by 250
Immunity and Inflammation in EpilepsyPreprint
Vezzani, A., Lang, B., & Aronica, E. (2015) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a022699 · Cited by 254
Rhee, S. H., & Hwang, D. H. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m007386200 · Cited by 247
Toll-like receptor signal transduction
Krishnan, J., Selvarajoo, K., Tsuchiya, M., Lee, G., & Choi, S. (2007) · Experimental & Molecular Medicine · doi:10.1038/emm.2007.47 · Cited by 252
“LPS is captured by LPS binding protein (LBP) in blood (Ulevitch and Tobias, 1995).”
Protein Kinase Cϵ Is Required for Macrophage Activation and Defense Against Bacterial Infection
Castrillo, A., Pennington, D. J., Otto, F., Parker, P. J., Owen, M. J., & Boscá, L. (2001) · The Journal of Experimental Medicine · doi:10.1084/jem.194.9.1231 · Cited by 244
Human MD-2 confers on mouse Toll-like receptor 4 species-specific lipopolysaccharide recognition
Akashi, S., Nagai, Y., Ogata, H., Oikawa, M., Fukase, K., Kusumoto, S., Kawasaki, K., Nishijima, M., Hayashi, S., Kimoto, M., et al. (2001) · International Immunology · doi:10.1093/intimm/13.12.1595 · Cited by 245
“LPS is a principal component of Gram-negative bacteria that activates the innate immune system and one of the best-studied molecules ( 3 ).”
BackgroundLiang, Y., Zhan, J., Liu, D., Luo, M., Han, J., Liu, X., Liu, C., Cheng, Z. Z., Zhou, Z., & Wang, P. (2019) · Microbiome · doi:10.1186/s40168-019-0635-4 · Cited by 248
Nau, R., & Eiffert, H. (2002) · Clinical Microbiology Reviews · doi:10.1128/cmr.15.1.95-110.2002 · Cited by 242
“LPS induces the release of a broad spectrum of inflammatory cytokines such as interleukin-1 (IL-1), IL-6, IL-8, and tumor necrosis factor alpha (TNF- ) from human peripheral mononuclear blood cells and expression of VCAM or ICAM on endothelial cells (21, 104, 105, 174, 175).”
BackgroundMyD88-deficient mice develop severe intestinal inflammation in dextran sodium sulfate colitis
Araki, A., Kanai∥, T., Ishikura, T., Makita, S., Uraushihara, K., Iiyama, R., Totsuka, T., Takeda, K., Akira, S., & Watanabe, M. (2005) · Journal of Gastroenterology · doi:10.1007/s00535-004-1492-9 · Cited by 239
Immunomodulatory properties of chitosan polymers
Moran, H. B. T., Turley, J. L., Andersson, M., & Lavelle, E. C. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.08.054 · Cited by 243
Initial and innate responses to viral infections — pattern setting in immunity or disease
Biron, C. A. (1999) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(99)80066-6 · Cited by 239
Sweeten PAMPs: Role of sugar complexed PAMPs in innate immunity and vaccine biology
Mahla, R. S. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00248 · Cited by 239
Cosenza;, M. A., Zhao;, M., Si;, Q., & Lee, S. C. (2002) · Brain Pathology · doi:10.1111/j.1750-3639.2002.tb00461.x · Cited by 238
“CD14 is the LPS receptor and renders the cells exquisitely sensitive to the actions of LPS, as is the case for microglia (35, 55, 63).”
BackgroundIn VitroBrucella suisInfection Prevents the Programmed Cell Death of Human Monocytic Cells
Gross, A., Terraza, A., Ouahrani‐Bettache, S., Liautard, J., & Dornand, J. (2000) · Infection and Immunity · doi:10.1128/iai.68.1.342-351.2000 · Cited by 237
“, in the absence of lipopolysaccharidebinding protein (LBP), which is necessary for LPS-induced monocyte activation during phagocytosis (43).”
BackgroundFazioli, F., Resnati, M., Sidénius, N., Higashimoto, Y., Appella, E., & Blasi, F. (1997) · The EMBO Journal · doi:10.1093/emboj/16.24.7279 · Cited by 237
Saitoh, S.-I. (2004) · International Immunology · doi:10.1093/intimm/dxh097 · Cited by 235
Importance of MAPK pathways for microglial pro-inflammatory cytokine IL-1β production
Kim, S. H., Smith, C. J., & Eldik, L. J. V. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(03)00126-x · Cited by 241
Comprehensive gene expression profile of LPS-stimulated human monocytes by SAGE
Suzuki, T., Hashimoto, S., Toyoda, N., Nagai, S., Yamazaki, N., Dong, H.-Y., Sakai, J., Yamashita, T., Nukiwa, T., & Matsushima, K. (2000) · Blood · doi:10.1182/blood.v96.7.2584 · Cited by 235
Human monocyte CD14 is upregulated by lipopolysaccharide
Landmann, R., Knopf, H. P., Link, S., Sansano, S., Schumann, R., & Zimmerli, W. (1996) · Infection and Immunity · doi:10.1128/iai.64.5.1762-1769.1996 · Cited by 234
Signaling Events Induced by Lipopolysaccharide-Activated Toll-Like Receptor 2
Yang, R., Mark, M. R., Gurney, A. L., & Godowski, P. J. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.163.2.639 · Cited by 234
Böttcher, M. F., Hmani‐Aifa, M., Lindström, A., Jenmalm, M. C., Mai, X., Nilsson, L. J., Zdolsek, H. A., Björkstén, B., Söderkvist, P., & Vaarala, O. (2004) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2004.04.050 · Cited by 229
Fish Oil Decreases Macrophage Tumor Necrosis Factor Gene Transcription by Altering the NFκB Activity
Lo, C.-J., Chiu, K. C., Fu, M., Lo, R., & Helton, S. W. (1999) · Journal of Surgical Research · doi:10.1006/jsre.1998.5524 · Cited by 234
Innate Immunity and Inflammation: A Transcriptional Paradigm
Hawiger, J. (2001) · Immunologic Research · doi:10.1385/ir:23:2-3:099 · Cited by 225
Lipopolysaccharide binding protein and soluble CD14 catalyze exchange of phospholipids.
Yu, B., Hailman, E., & Wright, S. D. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119160 · Cited by 225
Nishimura, T., Kitamura, H., Iwakabe, K., Yahata, T., Ohta, A., Sato, M., Takeda, K., Okumura, K., Kaer, L. V., Kawano, T., et al. (2000) · International Immunology · doi:10.1093/intimm/12.7.987 · Cited by 225
Matsumoto, S., Hara, T., Hori, T., Mitsuyama, K., Nagaoka, M., Tomiyasu, N., Suzuki, A., & Sata, M. (2005) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2005.02790.x · Cited by 224
How does peripheral lipopolysaccharide induce gene expression in the brain of rats?
Singh, A. K., & Jiang, Y. (2004) · Toxicology · doi:10.1016/j.tox.2004.04.015 · Cited by 223
Biological effects of bacterial lipopolysaccharide (endotoxin) in fish: A review
Swain, P., Nayak, S., Nanda, P. K., & DASH, S. (2008) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2008.04.009 · Cited by 229
Subchronic Exposure of Mice to Cadmium Perturbs Their Hepatic Energy Metabolism and Gut Microbiome
Zhang, S., Jin, Y., Zeng, Z., Liu, Z., & Fu, Z. (2015) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.5b00237 · Cited by 220
Pyo, H., Jou, I., Jung, S., Hong, S., & Joe, E.-H. (1998) · Neuroreport · doi:10.1097/00001756-199803300-00020 · Cited by 217
Effect of Lipopolysaccharide on Inflammation and Insulin Action in Human Muscle
Liang, H., Hussey, S. E., Sanchez-Avila, A., Tantiwong, P., & Musi, N. (2013) · PLoS ONE · doi:10.1371/journal.pone.0063983 · Cited by 215
“When LBP and sCD14 are absent, a much higher LPS concentration is required to exert its cellular effects [36,37].”
BackgroundGenomic polymorphisms in sepsis
Lin, M. T., & Albertson, T. E. (2004) · Critical Care Medicine · doi:10.1097/01.ccm.0000110878.49476.42 · Cited by 217
Gut Microbiota: The Conductor in the Orchestra of Immune–Neuroendocrine Communication
El Aidy, S., Dinan, T. G., & Cryan, J. F. (2015) · Clinical Therapeutics · doi:10.1016/j.clinthera.2015.03.002 · Cited by 215
“May 2015 microbiota stimulates a chronic state of low-level activation of the (innate) immune system in the host, in which bacterial particles stimulate intestinal macrophages and T cells to produce pro-inflammatory cytokines (eg, interleukin [IL]-1β, tumor necrosis factor-α, IL-18).(48,49) The produced cytokines crea…”
BackgroundOral Inflammatory Diseases and Systemic Inflammation: Role of the Macrophage
Hastürk, H., Kantarcı, A., & Dyke, T. E. V. (2012) · Frontiers in Immunology · doi:10.3389/fimmu.2012.00118 · Cited by 215
“While CD14 is the major LBP on the surface of mononuclear phagocytes, CD14 is not capable of transducing signals across the membrane.”
BackgroundInfluentialAntagonistic antibody prevents toll-like receptor 2–driven lethal shock-like syndromes
Meng, G., Rutz, M., Schiemann, M., Metzger, J., Grabiec, A., Schwandner, R., Luppa, P. B., Ebel, F., Busch, D. H., Bauer, S., et al. (2004) · Journal of Clinical Investigation · doi:10.1172/jci20762 · Cited by 211
Pugin, J., Widmer, M.-C., Kossodo, S. D., Liang, C.-M., Preas, H. L., & Suffredini, A. F. (1999) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/ajrcmb.20.3.3311 · Cited by 212
Anthrolysin O and Other Gram-positive Cytolysins Are Toll-like Receptor 4 Agonists
Park, J. M., Ng, V. H., Maeda, S., Rest, R. F., & Karin, M. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20041215 · Cited by 212
“TLR4 activation by LPS depends strictly on factors such as soluble CD14 and LPS-binding protein that are provided by inclusion of serum (18).”
BackgroundA Review of Bioactive Factors in Human Breastmilk: A Focus on Prematurity
Gila-Díaz, A., Arribas, S. M., Algara, A., Martin-Cabrejas, M. A., de Pablo, Á. L. L., de Pipaón, M. S., & Ramiro‐Cortijo, D. (2019) · Nutrients · doi:10.3390/nu11061307 · Cited by 212
“This latter membrane-bound form is primarily expressed on the surface of monocytes, macrophages and neutrophils [95,96].”
BackgroundRosenberger, C. M., Scott, M. G., Gold, M. R., Hancock, R. E. W., & Finlay, B. B. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.11.5894 · Cited by 209
TLR2: cellular sensor for microbial and endogenous molecular patterns.
Kirschning, C., & Schumann, R. (2002) · Current Topics in Microbiology and Immunology · doi:10.1007/978-3-642-59430-4_8 · Cited by 232
Mammalian GPI proteins: sorting, membrane residence and functions
Nosjean, O., Briolay, A., & Roux, B. (1997) · Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes · doi:10.1016/s0304-4157(97)00005-1 · Cited by 211
Netea, M. G., Fantuzzi, G., Kullberg, B. J., Stuyt, R. J. L., Pulido, E. J., McIntyre, R. C., Joosten, L. A. B., van der Meer, J. W. M., & Dinarello, C. A. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.5.2644 · Cited by 210
“(35), it is not surprising that differences in the structure of lipid A”
BackgroundAndreakos, E., Sacre, S. M., Smith, C., Lundberg, A. M., Kiriakidis, S., Stonehouse, T., Monaco, C. G., Feldmann, M., & Foxwell, B. M. J. (2003) · Blood · doi:10.1182/blood-2003-04-1356 · Cited by 214
Yang, S., Tamai, R., Akashi, S., Takeuchi, O., Akira, S., Sugawara, S., & Takada, H. (2001) · Infection and Immunity · doi:10.1128/iai.69.4.2045-2053.2001 · Cited by 207
Muta, T., & Takeshige, K. (2001) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2001.02385.x · Cited by 205
Chaston, J. M., Suen, G., Tucker, S., Andersen, A. W., Bhasin, A., Bode, E., Bode, H. B., Brachmann, A. O., Cowles, C. E., Cowles, K. N., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027909 · Cited by 214
Surfactant Proteins A and D Bind CD14 by Different Mechanisms
Sano, H. I., Chiba, H., Iwaki, D., Sohma, H., Voelker, D. R., & Kuroki, Y. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m001107200 · Cited by 205
Dixon, D. R., & Darveau, R. P. (2005) · Journal of Dental Research · doi:10.1177/154405910508400702 · Cited by 203
“For example, early in vitro studies suggested that TLR2 could interact with mCD14—that had previously recognized LBP-bound bacterial LPS (Wright et al., 1990; Ulevitch and Tobias, 1995)—forming an LPS/receptor complex (Yang et al.”
BackgroundRuggiero, T., Trabucchi, M., Santa, F. D., Zupo, S., Harfe, B. D., McManus, M. T., Rosenfeld, M. G., Briata, P., & Gherzi, R. (2009) · The FASEB Journal · doi:10.1096/fj.09-131342 · Cited by 203
“regarded as the cause of septic shock (10).”
BackgroundHan, Z., Enslen, H., Hu, X., Meng, X.-J., Wu, I.-H., Barrett, T., Davis, R., & Ip, Y. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.6.3527 · Cited by 207
Sellati, T. J., Bouis, D. A., Kitchens, R. L., Darveau, R. P., Pugin, J., Ulevitch, R. J., Gangloff, S. C., Goyert, S. M., Norgard, M. V., & Radolf, J. D. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.160.11.5455 · Cited by 201
Self-citationSAPK/JNK activation and apoptotic induction by the macrophage P2X7 nucleotide receptor
Humphreys, B. D. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m002770200 · Cited by 199
Role of CD14 in Cellular Recognition of Bacterial Lipopolysaccharides
Kitchens, R. L. (1999) · KARGER eBooks · doi:10.1159/000058750 · Cited by 197
CYTOKINE EXPRESSION IN THREE MOUSE MODELS OF EXPERIMENTAL HEPATITIS
Sass, G., Heinlein, S., Agli, A., Bang, R., Schümann, J., & Tiegs, G. (2002) · Cytokine · doi:10.1006/cyto.2002.1948 · Cited by 197
Toll-like receptors: a family of pattern-recognition receptors in mammals.
Armant, M. A., & Fenton, M. J. (2002) · Genome biology · doi:10.1186/gb-2002-3-8-reviews3011 · Cited by 196
Tollip Regulates Proinflammatory Responses to Interleukin-1 and Lipopolysaccharide
Didierlaurent, A. M., Brissoni, B., Velin, D., Aebi, N., Tardivel, A., Käslin, E., Sirard, J., Angelov, G. S., Tschopp, J., & Burns, K. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.26.3.735-742.2006 · Cited by 195
“However, excessive and prolonged activation of innate immunity is harmful to the host and may even be fatal (17).”
BackgroundCatalytic Properties of Lipopolysaccharide (LPS) Binding Protein
Yu, B., & Wright, S. D. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.8.4100 · Cited by 195
Itoh, K., Udagawa, N., Kobayashi, K., Suda, K., Li, X., Takami, M., Okahashi, N., Nishihara, T., & Takahashi, N. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.7.3688 · Cited by 193
Elass, E., Legrand, D., Salmon, V., Roșeanu, A., Trif, M., Tobias, P. S., Mazurier, J., & Spik, G. (1998) · Infection and Immunity · doi:10.1128/iai.66.2.486-491.1998 · Cited by 193
Self-citationShi, C., Shi, G., Hsiao, H.-M., Kao, Y.-C., Kuo, K.-L., Ma, C.-Y., Kuo, C., Chang, B.-I., Chang, C., Lin, C., et al. (2008) · Blood · doi:10.1182/blood-2008-03-142760 · Cited by 192
“Binding of LPS to TLR4 triggers the activation of members of the mitogen-activated protein kinase (MAPK) pathway including p38, p42/p44 extra-cellular signal-regulated kinase (ERK1/2), and c-Jun N-terminal kinase (JNK).(8) In resting un-stimulated cells, nuclear factor-κB (NF-κB), a heterodimeric complex composed of 5…”
BackgroundHubacek, J. A., Stüber, F., Fröhlich, D., Book, M., Wetegrove, S., Ritter, M., Rothe, G., & Schmitz, G. (2001) · Critical Care Medicine · doi:10.1097/00003246-200103000-00015 · Cited by 190
Suppression of the inflammatory response by triterpenes isolated from the mushroom Ganoderma lucidum
Dudhgaonkar, S. P., Thyagarajan‐Sahu, A., & Slíva, D. (2009) · International Immunopharmacology · doi:10.1016/j.intimp.2009.07.011 · Cited by 193
“The MAP kinases ERK1/2, JNK and p38 are induced by LPS and can therefore regulate the activity of AP-1 and NF-κB [33].”
BackgroundInfluentialLuo, R., Yao, Y., Chen, Z., & Sun, X. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02149-4 · Cited by 207
“The concave surface, formed by 11 parallel and two antiparallel strands, requires N-terminal disulfide bonds and glycosylation for proper folding and signaling [31, 32].”
Arimoto, T., & Bing, G. (2003) · Neurobiology of Disease · doi:10.1016/s0969-9961(02)00017-7 · Cited by 202
Nagai, Y., Shimazu, R., Ogata, H., Akashi, S., Sudo, K., Yamasaki, H., Hayashi, S., Iwakura, Y., Kimoto, M., & Miyake, K. (2002) · Blood · doi:10.1182/blood.v99.5.1699 · Cited by 189
Heritability estimates of innate immunity: an extended twin study
de Craen, A. J. M., Posthuma, D., Remarque, E. J., van den Biggelaar, A. H. J., Westendorp, R. G. J., & Boomsma, D. I. (2005) · Genes and Immunity · doi:10.1038/sj.gene.6364162 · Cited by 187
“After LPS activation through Toll-like receptor (TLR-) 4, innate immune cells immediately produce a variety of inflammatory mediators such as interleukin (IL-)1β, IL-1 receptor antagonist (ra), IL-6, IL-10, and tumor necrosis factor (TNF-) α”
BackgroundDiep, D. B., Nelson, K. L., Raja, S. M., Pleshak, E. N., & Buckley, J. T. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.4.2355 · Cited by 186
Pulmonary collectins in innate immunity of the lung
Kuroki, Y., Takahashi, M., & Nishitani, C. (2007) · Cellular Microbiology · doi:10.1111/j.1462-5822.2007.00953.x · Cited by 184
“LPS is a major constituent of the outer membrane of Gram-negative bacteria, and is a potent stimulant of inflammation (Ulevitch and Tobias, 1995).”
BackgroundMartin, M., Katz, J., Vogel, S. N., & Michalek, S. M. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.9.5278 · Cited by 183
“A major constituent of the outer membrane of Gram-negative bacteria is LPS, which is considered to be a potent inducer of proinflammatory cytokines by neutrophils, monocytes, and macrophages (1, 2).”
BackgroundBannerman, D. D., Sathyamoorthy, M., & Goldblum, S. E. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.52.35371 · Cited by 183
Sano, H. I., Sohma, H., Muta, T., Nomura, S.-I., Voelker, D. R., & Kuroki, Y. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.163.1.387 · Cited by 183
Yan, F., Wang, L., Shi, Y., Cao, H., Liu, L., Washington, M. K., Chaturvedi, R., Israel, D. A., Cao, H., Wang, B., et al. (2011) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00312.2011 · Cited by 182
Neutrophil Priming in Host Defense: Role of Oxidants as Priming Agents
Swain, S. D., Rohn, T. T., & Quinn, M. T. (2002) · Antioxidants and Redox Signaling · doi:10.1089/152308602753625870 · Cited by 181
“LPS, a component of the cell wall of gram-negative bacteria, is a potent inflammatory mediator, which induces production of proinflammatory cytokines and functional alterations in many cells during sepsis (72).”
Yu, Y.-H., He, J., Li, S., Song, L., Guo, X., Yao, W., Zou, D., Gao, X., Liu, Y., Bai, F., et al. (2016) · International Immunopharmacology · doi:10.1016/j.intimp.2016.05.026 · Cited by 182
Endotoxin Down-Regulates T Cell Activation by Antigen-Presenting Liver Sinusoidal Endothelial Cells
Knolle, P. A., Germann, T., Treichel, U., Uhrig, A., Schmitt, E., Hegenbarth, S. I., Lohse, A. W., & Gerken, G. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.3.1401 · Cited by 181
Glycine: a new anti-inflammatory immunonutrient
Wheeler, M. D., Ikejema, K., Enomoto, N., Stacklewitz, R. F., Seabra, V., Zhong, Z., Yin, M., Schemmer, P., Rose, M., Rusyn, I., et al. (1999) · Cellular and Molecular Life Sciences · doi:10.1007/s000180050030 · Cited by 178
Terato, K., Harper, D. S., Griffiths, M. M., Hasty, D. L., Ye, X. J., Cremer, M. A., & Seyer, J. M. (1995) · Autoimmunity · doi:10.3109/08916939508995311 · Cited by 178
Muzio, M., Polentarutti, N., Bosisio, D., Prahladan, M. K. P., & Mantovani, A. (2000) · Journal of Leukocyte Biology · doi:10.1002/jlb.67.4.450 · Cited by 176
“Alternatively, the LBP/LPS complex can be recognized by a soluble version of CD14; this trimolecular complex can subsequently activate non-myeloid cells such as endothelial and epithelial cells.”
BackgroundBainbridge, B. W., & Darveau, R. P. (2001) · Acta Odontologica Scandinavica · doi:10.1080/000163501750266710 · Cited by 175
Role of cytokines in testicular function
Hales, D. B., Thorsten Diemer, A., & Hales, K. H. (1999) · Endocrine · doi:10.1007/bf02738619 · Cited by 173
Metadata
- Authors
- Ulevitch, R. J., & Tobias, P. S.
- Affiliations
- Scripps Research Institute (US)
- ORCID
- Ulevitch, R J
- Venue
- Annual Review of Immunology
- Publisher
- Annual Reviews
- Published
- 1995-04
- Volume
- 13
- Issue
- 1
- Pages
- 437-457
- ISSN
- 0732-0582 (ISSN-L)
- 1545-3278
- OpenAlex
- W2113828544
- Cited by
- 1,442
- References
- 36
- Citations by year
- 2026: 4 · 2025: 11 · 2024: 8 · 2023: 11 · 2022: 13 · 2021: 25 · 2020: 23 · 2019: 21 · 2018: 22 · 2017: 24 · 2016: 37 · 2015: 29 · 2014: 39 · 2013: 43 · 2012: 38
- FWCI
- 20.96
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Immunology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (GM28485, GM3769)
- National Institute of Allergy and Infectious Diseases (AI 15136, R01AI015136)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Health Sciences › Medicine › Critical Care and Intensive Care Medicine › Sepsis Diagnosis and Treatment
- Life Sciences › Immunology and Microbiology › Immunology › Inflammation biomarkers and pathways
- Keywords
- lipopolysaccharide, endotoxin, LPS receptor, CD14, LPS-binding protein, septic shock, myeloid cells, intracellular signaling, transmembrane proteins, pro-inflammatory mediators
- MeSH terms
- Lipopolysaccharide-Binding Protein, Acute-Phase Proteins, Amino Acid Sequence, Animals, Carbohydrate Sequence, Carrier Proteins, Humans, Lipopolysaccharides, Membrane Glycoproteins, Models, Biological, Molecular Sequence Data, Receptors, Immunologic, Shock, Septic, Antigens, Differentiation, Myelomonocytic, Molecular Structure, Signal Transduction, Antigens, CD, Calcium-Calmodulin-Dependent Protein Kinases, Lipopolysaccharide Receptors
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