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Entamoeba histolytica Trophozoites and Lipopeptidophosphoglycan Trigger Human Neutrophil Extracellular Traps

https://doi.org/10.1371/journal.pone.0158979
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s00281-012-0349-1openalex-snapshot
The dynamic interdependence of amebiasis, innate immunity, and undernutrition
inferredcites →https://doi.org/10.1007/s00281-013-0380-xopenalex-snapshot
Modulation of neutrophil NETosis: interplay between infectious agents and underlying host physiology
inferredcites →https://doi.org/10.1007/s00436-014-3939-0openalex-snapshot
The apicomplexan parasite Eimeria arloingi induces caprine neutrophil extracellular traps
inferredcites →https://doi.org/10.1016/0035-9203(78)90144-xopenalex-snapshot
A new medium for the axenic cultivation of Entamoeba histolytica and other Entamoeba
inferredcites →https://doi.org/10.1016/j.arcmed.2005.10.007openalex-snapshot
Pathogenesis of Acute Experimental Liver Amebiasis
inferredcites →https://doi.org/10.1016/j.cub.2005.12.039openalex-snapshot
DNase Expression Allows the Pathogen Group A Streptococcus to Escape Killing in Neutrophil Extracellular Traps
inferredcites →https://doi.org/10.1016/j.exppara.2012.12.009openalex-snapshot
Effect of antimicrobial peptides derived from human cathelicidin LL-37 on Entamoeba histolytica trophozoites
inferredcites →https://doi.org/10.1016/j.it.2009.07.011openalex-snapshot
NETs: a new strategy for using old weapons
inferredcites →https://doi.org/10.1016/j.yexmp.2006.09.005openalex-snapshot
Late experimental amebic liver abscess in hamster is inhibited by cyclosporine and N-acetylcysteine
inferredcites →https://doi.org/10.1016/s0014-4894(02)00021-8openalex-snapshot
Entamoeba histolytica: immunohistochemical study of hepatic amoebiasis in mouse. Neutrophils and nitric oxide as possible factors of resistance
inferredcites →https://doi.org/10.1016/s0016-5085(98)70023-xopenalex-snapshot
Epithelial cell–initiated inflammation plays a crucial role in early tissue damage in amebic infection of human intestine
inferredcites →https://doi.org/10.1016/s0140-6736(07)61690-0openalex-snapshot
Maternal and child undernutrition: global and regional exposures and health consequences
inferredcites →https://doi.org/10.1016/s0140-6736(12)61728-0openalex-snapshot
Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010
inferredcites →https://doi.org/10.1016/s0166-6851(03)00160-9openalex-snapshot
Leishmania lipophosphoglycan (LPG) activates NK cells through toll-like receptor-2
inferredcites →https://doi.org/10.1038/168167a0openalex-snapshot
A Colorimetric Method for the Determination of Sugars
inferredcites →https://doi.org/10.1038/nm.1959openalex-snapshot
Netting neutrophils in autoimmune small-vessel vasculitis
inferredcites →https://doi.org/10.1038/nm1565openalex-snapshot
Platelet TLR4 activates neutrophil extracellular traps to ensnare bacteria in septic blood
inferredcites →https://doi.org/10.1038/nrmicro1710openalex-snapshot
Beneficial suicide: why neutrophils die to make NETs
inferredcites →https://doi.org/10.1046/j.1365-3024.1998.00128.xopenalex-snapshot
Role of neutrophils in innate resistance to Entamoeba histolytica liver infection in mice
inferredcites →https://doi.org/10.1073/pnas.0900226106openalex-snapshot
Leishmania amazonensis promastigotes induce and are killed by neutrophil extracellular traps
inferredcites →https://doi.org/10.1083/jcb.200606027openalex-snapshot
Novel cell death program leads to neutrophil extracellular traps
inferredcites →https://doi.org/10.1089/sur.2008.011openalex-snapshot
Polymorphonuclear Neutrophil Infiltration Intensity as Consequence of Entamoeba histolytica Density in Amebic Colitis
inferredcites →https://doi.org/10.1093/clinids/8.2.228openalex-snapshot
Problems in Recognition and Diagnosis of Amebiasis: Estimation of the Global Magnitude of Morbidity and Mortality
inferredcites →https://doi.org/10.1093/infdis/154.1.19openalex-snapshot
The Interaction of Human Neutrophils and Entamoeba histolytica Increases Cytopathogenicity for Liver Cell Monolayers
inferredcites →https://doi.org/10.1093/infdis/jiv031openalex-snapshot
A Thermonuclease of Neisseria gonorrhoeae Enhances Bacterial Escape From Killing by Neutrophil Extracellular Traps
inferredcites →https://doi.org/10.1099/mic.0.000040openalex-snapshot
Identification of a novel DNase of Streptococcus suis (EndAsuis) important for neutrophil extracellular trap degradation during exponential growth
inferredcites →https://doi.org/10.1111/j.1365-3024.2005.00754.xopenalex-snapshot
The innate immune response to Entamoeba histolytica lipopeptidophosphoglycan is mediated by toll‐like receptors 2 and 4
inferredcites →https://doi.org/10.1111/j.1365-3024.2007.00963.xopenalex-snapshot
Lipopopeptidephosphoglycan from Entamoeba histolytica activates human macrophages and dendritic cells and reaches their late endosomes
inferredcites →https://doi.org/10.1111/j.1365-3024.2011.01333.xopenalex-snapshot
Absence of CD38 delays arrival of neutrophils to the liver and innate immune response development during hepatic amoebiasis by Entamoeba histolytica
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.07419.xopenalex-snapshot
Characterization of the restriction enzyme‐like endonuclease encoded by the Entamoeba histolytica non‐long terminal repeat retrotransposon EhLINE1
inferredcites →https://doi.org/10.1111/mmi.12295openalex-snapshot
N uclease A ( Gbs 0661), an extracellular nuclease of S treptococcus agalactiae, attacks the neutrophil extracellular traps and is needed for full virulence
inferredcites →https://doi.org/10.1126/science.1092385openalex-snapshot
Neutrophil Extracellular Traps Kill Bacteria
inferredcites →https://doi.org/10.1126/science.1242255openalex-snapshot
Staphylococcus aureus Degrades Neutrophil Extracellular Traps to Promote Immune Cell Death
inferredcites →https://doi.org/10.1126/scitranslmed.3001180openalex-snapshot
Neutrophils Activate Plasmacytoid Dendritic Cells by Releasing Self-DNA–Peptide Complexes in Systemic Lupus Erythematosus
inferredcites →https://doi.org/10.1128/cmr.13.2.318openalex-snapshot
Pathogenesis of Intestinal Amebiasis: From Molecules to Disease
inferredcites →https://doi.org/10.1128/iai.01232-13openalex-snapshot
3′-Nucleotidase/Nuclease Activity Allows Leishmania Parasites To Escape Killing by Neutrophil Extracellular Traps
inferredcites →https://doi.org/10.1128/iai.05730-11openalex-snapshot
Toxoplasma gondii Triggers Release of Human and Mouse Neutrophil Extracellular Traps
inferredcites →https://doi.org/10.1128/iai.65.9.3951-3953.1997openalex-snapshot
Neutrophils play a critical role in early resistance to amebic liver abscesses in severe combined immunodeficient mice
inferredcites →https://doi.org/10.1128/iai.73.8.4522-4529.2005openalex-snapshot
Resistance to Intestinal Entamoeba histolytica Infection Is Conferred by Innate Immunity and Gr-1 + Cells
inferredcites →https://doi.org/10.1128/mbio.01817-14openalex-snapshot
Bone Marrow Dendritic Cells from Mice with an Altered Microbiota Provide Interleukin 17A-Dependent Protection against Entamoeba histolytica Colitis
inferredcites →https://doi.org/10.1128/mbio.02046-14openalex-snapshot
Leptin Receptor Mutation Results in Defective Neutrophil Recruitment to the Colon during Entamoeba histolytica Infection
inferredcites →https://doi.org/10.1134/s0006297914120025openalex-snapshot
Neutrophil Extracellular Traps: Mechanisms of formation and role in health and disease
inferredcites →https://doi.org/10.1146/annurev-immunol-020711-074942openalex-snapshot
Neutrophil Function: From Mechanisms to Disease
inferredcites →https://doi.org/10.1159/000319909openalex-snapshot
Nuclease Expression by Staphylococcus aureus Facilitates Escape from Neutrophil Extracellular Traps
inferredcites →https://doi.org/10.1182/blood-2013-04-457671openalex-snapshot
NETosis: how vital is it?
inferredcites →https://doi.org/10.1182/blood.v97.12.3951openalex-snapshot
Human cathelicidin, hCAP-18, is processed to the antimicrobial peptide LL-37 by extracellular cleavage with proteinase 3
inferredcites →https://doi.org/10.1186/1475-2875-7-41openalex-snapshot
Cytokine-associated neutrophil extracellular traps and antinuclear antibodies in Plasmodium falciparum infected children under six years of age
inferredcites →https://doi.org/10.1371/journal.pone.0070363openalex-snapshot
Competence-Independent Activity of Pneumococcal Enda Mediates Degradation of Extracellular DNA and Nets and Is Important for Virulence
inferredcites →https://doi.org/10.1371/journal.pone.0103125openalex-snapshot
Cell Wall-Anchored Nuclease of Streptococcus sanguinis Contributes to Escape from Neutrophil Extracellular Trap-Mediated Bacteriocidal Activity
inferredcites →https://doi.org/10.1371/journal.pone.0139569openalex-snapshot
Trypanosoma cruzi and Its Soluble Antigens Induce NET Release by Stimulating Toll-Like Receptors
inferredcites →https://doi.org/10.1371/journal.ppat.1000434openalex-snapshot
Natural Killer T Cells Activated by a Lipopeptidophosphoglycan from Entamoeba histolytica Are Critically Important To Control Amebic Liver Abscess
inferredcites →https://doi.org/10.1371/journal.ppat.1003614openalex-snapshot
Vibrio cholerae Evades Neutrophil Extracellular Traps by the Activity of Two Extracellular Nucleases
inferredcites →https://doi.org/10.1371/journal.ppat.1004929openalex-snapshot
Rapid Sequestration of Leishmania mexicana by Neutrophils Contributes to the Development of Chronic Lesion
inferredcites →https://doi.org/10.2307/3282753openalex-snapshot
Pathogenesis of Acute Experimental Amebic Liver Abscess in Hamsters
inferredcites →https://doi.org/10.4049/jimmunol.1000893openalex-snapshot
Leishmania donovani Promastigotes Evade the Antimicrobial Activity of Neutrophil Extracellular Traps

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Neutrophils vs. amoebas: Immunity against the protozoan parasiteEntamoeba histolytica
inferred← citeshttps://doi.org/10.1002/jlb.ma0818-309rrropenalex-snapshot
Pathogenic Entamoeba histolytica, but not Entamoeba dispar, induce neutrophil extracellular trap (NET) formation
inferred← citeshttps://doi.org/10.1007/978-3-030-44826-4_13openalex-snapshot
Role of Extracellular Traps Promoted by Intestinal Parasites. Relationship with Virulence
inferred← citeshttps://doi.org/10.1007/s00436-022-07475-xopenalex-snapshot
Trichomonas vaginalis triggers neutrophil extracellular traps reducing parasite integrity and growth
inferred← citeshttps://doi.org/10.1007/s00436-024-08149-6openalex-snapshot
Revisiting the isolation and characterisation of Entamoeba histolytica lipopeptidophosphoglycan
inferred← citeshttps://doi.org/10.1007/s12016-021-08861-6openalex-snapshot
Significance of Mast Cell Formed Extracellular Traps in Microbial Defense
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The interaction of gut microbiota with parasitic protozoa
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Entamoeba
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Host Immune Responses Against Intestinal Unicellular Parasites and Their Role in Pathogenesis and Protection
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Entamoeba histolytica: Plasma membrane components and virulence factors in the invasive process
inferred← citeshttps://doi.org/10.1016/j.cellimm.2022.104630openalex-snapshot
Trichinella spiralis excretory-secretory antigens selectively inhibit the release of extracellular traps from neutrophils without affecting their additional antimicrobial functions
inferred← citeshttps://doi.org/10.1016/j.cellimm.2022.104640openalex-snapshot
Neutrophil extracellular traps: Modulation mechanisms by pathogens
inferred← citeshttps://doi.org/10.1016/j.dci.2017.02.020openalex-snapshot
Molecular analyses on Neospora caninum -triggered NETosis in the caprine system
inferred← citeshttps://doi.org/10.1016/j.dci.2020.103787openalex-snapshot
Fasciola hepatica induces weak NETosis and low production of intra- and extracellular ROS in exposed bovine polymorphonuclear neutrophils
inferred← citeshttps://doi.org/10.1016/j.ejop.2023.126032openalex-snapshot
Acanthamoeba castellanii trophozoites escape killing by neutrophil extracellular traps using their 3′-nucleotidase/nuclease activity
inferred← citeshttps://doi.org/10.1016/j.intimp.2022.109448openalex-snapshot
Protein Kinase C Isoforms Mediate the Formation of Neutrophil Extracellular Traps
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.110100openalex-snapshot
Entamoeba histolytica induced NETosis and the dual role of NETs in amoebiasis
inferred← citeshttps://doi.org/10.1016/j.jevs.2018.11.002openalex-snapshot
Extracellular Trap Formation by Donkey Polymorphonuclear Neutrophils Against Toxoplasma gondii
inferred← citeshttps://doi.org/10.1016/j.pt.2020.09.015openalex-snapshot
Host Protective Mechanisms to Intestinal Amebiasis
inferred← citeshttps://doi.org/10.1016/j.vetimm.2017.05.005openalex-snapshot
Role of NETs in the difference in host susceptibility to Toxoplasma gondii between sheep and cattle
inferred← citeshttps://doi.org/10.1042/bsr20180916openalex-snapshot
The state of art of neutrophil extracellular traps in protozoan and helminthic infections
inferred← citeshttps://doi.org/10.1080/21505594.2022.2158656openalex-snapshot
Pathogenicity and virulence of Entamoeba histolytica , the agent of amoebiasis
inferred← citeshttps://doi.org/10.1080/21505594.2023.2289775openalex-snapshot
Unraveling the interplay between unicellular parasites and bacterial biofilms: Implications for disease persistence and antibiotic resistance
inferred← citeshttps://doi.org/10.1111/pim.12714openalex-snapshot
Neutrophil extracellular traps and MPO in models of susceptibility and resistance against Entamoeba histolytica
inferred← citeshttps://doi.org/10.1152/physiol.00038.2019openalex-snapshot
Immune Response to the Enteric ParasiteEntamoeba histolytica
inferred← citeshttps://doi.org/10.1242/jcs.241075openalex-snapshot
The power from within – understanding the driving forces of neutrophil extracellular trap formation
inferred← citeshttps://doi.org/10.31579/2643-6612/042openalex-snapshot
Microscopy Analyses Reveal the Parasitism of Entamoeba gingivalis in Periodontitis: An Observational Study
inferred← citeshttps://doi.org/10.3389/fcimb.2017.00086openalex-snapshot
Streptococcus suis Serotype 2 Biofilms Inhibit the Formation of Neutrophil Extracellular Traps
inferred← citeshttps://doi.org/10.3389/fcimb.2018.00184openalex-snapshot
Entamoeba histolytica Trophozoites Induce a Rapid Non-classical NETosis Mechanism Independent of NOX2-Derived Reactive Oxygen Species and PAD4 Activity
inferred← citeshttps://doi.org/10.3389/fcimb.2018.00226openalex-snapshot
Entamoeba histolytica Induce Signaling via Raf/MEK/ERK for Neutrophil Extracellular Trap (NET) Formation
inferred← citeshttps://doi.org/10.3389/fcimb.2018.00315openalex-snapshot
Non-vesicular Lipid Transport Machinery in Entamoeba histolytica
inferred← citeshttps://doi.org/10.3389/fcimb.2022.1018314openalex-snapshot
Immunomodulatory effect of extracellular vesicles from Entamoeba histolytica trophozoites: Regulation of NETs and respiratory burst during confrontation with human neutrophils
inferred← citeshttps://doi.org/10.3389/fcimb.2022.855797openalex-snapshot
Molecular interplays of the Entamoeba histolytica endosomal sorting complexes required for transport during phagocytosis
inferred← citeshttps://doi.org/10.3389/fimmu.2022.900553openalex-snapshot
Gasdermins in Innate Host Defense Against Entamoeba histolytica and Other Protozoan Parasites
inferred← citeshttps://doi.org/10.3389/fimmu.2024.1493946openalex-snapshot
Entamoeba histolytica-induced NETs are highly cytotoxic on hepatic and colonic cells due to serine proteases and myeloperoxidase activities
inferred← citeshttps://doi.org/10.3390/antiox10060974openalex-snapshot
New Insights on NETosis Induced by Entamoeba histolytica: Dependence on ROS from Amoebas and Extracellular MPO Activity
inferred← citeshttps://doi.org/10.3390/ijms24108975openalex-snapshot
NETosis in Parasitic Infections: A Puzzle That Remains Unsolved
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The CAMKK/AMPK Pathway Contributes to Besnoitia besnoiti-Induced NETosis in Bovine Polymorphonuclear Neutrophils
inferred← citeshttps://doi.org/10.3390/membranes12111079openalex-snapshot
Entamoeba histolytica: Membrane and Non-Membrane Protein Structure, Function, Immune Response Interaction, and Vaccine Development
inferred← citeshttps://doi.org/10.3390/microorganisms12040827openalex-snapshot
Neutrophils versus Protozoan Parasites: Plasmodium, Trichomonas, Leishmania, Trypanosoma, and Entameoba
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Diversity and Plasticity of Virulent Characteristics of Entamoeba histolytica
inferred← citeshttps://doi.org/10.5152/tpd.2018.5952openalex-snapshot
Comparison of Picogreen and Sytox Orange Stains in Quantitative Analysis of Extracellular Trap Formed against Toxoplasma gondii in Polymorphonuclear Leukocytes from Sheep
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Beneficial and Deleterious Effects of Neutrophil Extracellular Traps on Infection
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Distinct temporal patterns of liver immune responses to pathogenic and non-pathogenic Entamoeba histolytica clones
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Etude de la nétose du polynucléaire neutrophile dans deux modèles de réactions allergiques : le choc anaphylactique aux curares et l’asthme
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