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DC-SIGN and CLEC-2 Mediate Human Immunodeficiency Virus Type 1 Capture by Platelets

https://doi.org/10.1128/jvi.00136-06
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What this work says

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

inferredcites →https://doi.org/10.1002/1521-4141(200002)30:2<697::aid-immu697>3.0.co;2-mopenalex-snapshot
Molecular characterization of two novel C-type lectin-like receptors, one of which is selectively expressed in human dendritic cells
inferredcites →https://doi.org/10.1002/cbf.1113openalex-snapshot
HCV infective virions can be carried by human platelets
inferredcites →https://doi.org/10.1002/path.1026openalex-snapshot
Placental expression of DC‐SIGN may mediate intrauterine vertical transmission of HIV
inferredcites →https://doi.org/10.1006/viro.1995.1016openalex-snapshot
Vpr Is Required for Efficient Replication of Human Immunodeficiency Virus Type-1 in Mononuclear Phagocytes
inferredcites →https://doi.org/10.1006/viro.1996.0206openalex-snapshot
The Amount of Host HLA-DR Proteins Acquired by HIV-1 Is Virus Strain- and Cell Type-Specific
inferredcites →https://doi.org/10.1006/viro.2000.0193openalex-snapshot
Productive Infection of CD34+-Cell-Derived Megakaryocytes by X4 and R5 HIV-1 Isolates
inferredcites →https://doi.org/10.1006/viro.2002.1730openalex-snapshot
DC-SIGN and DC-SIGNR Bind Ebola Glycoproteins and Enhance Infection of Macrophages and Endothelial Cells
inferredcites →https://doi.org/10.1016/j.micinf.2004.02.004openalex-snapshot
Syndecans and HIV-1 pathogenesis
inferredcites →https://doi.org/10.1016/j.virol.2003.09.028openalex-snapshot
Raji B cells, misidentified as THP-1 cells, stimulate DC-SIGN-mediated HIV transmission
inferredcites →https://doi.org/10.1016/j.virol.2004.05.022openalex-snapshot
Quantification of infectious HIV-1 plasma viral load using a boosted in vitro infection protocol
inferredcites →https://doi.org/10.1016/s0092-8674(00)80693-5openalex-snapshot
Identification of DC-SIGN, a Novel Dendritic Cell–Specific ICAM-3 Receptor that Supports Primary Immune Responses
inferredcites →https://doi.org/10.1016/s0092-8674(00)80694-7openalex-snapshot
DC-SIGN, a Dendritic Cell–Specific HIV-1-Binding Protein that Enhances trans-Infection of T Cells
inferredcites →https://doi.org/10.1016/s0092-8674(01)00477-9openalex-snapshot
Complement-Independent, Peroxide-Induced Antibody Lysis of Platelets in HIV-1-Related Immune Thrombocytopenia
inferredcites →https://doi.org/10.1016/s0966-842x(99)01474-2openalex-snapshot
HIV-1 attachment: another look
inferredcites →https://doi.org/10.1016/s1074-7613(02)00259-5openalex-snapshot
DC-SIGN-Mediated Internalization of HIV Is Required for Trans-Enhancement of T Cell Infection
inferredcites →https://doi.org/10.1038/79815openalex-snapshot
DC-SIGN–ICAM-2 interaction mediates dendritic cell trafficking
inferredcites →https://doi.org/10.1038/82161openalex-snapshot
Efficient presentation of exogenous antigen by liver endothelial cells to CD8+ T cells results in antigen-specific T-cell tolerance
inferredcites →https://doi.org/10.1038/ni841openalex-snapshot
Diversity of receptors binding HIV on dendritic cell subsets
inferredcites →https://doi.org/10.1038/nm1246openalex-snapshot
TLR activation triggers the rapid differentiation of monocytes into macrophages and dendritic cells
inferredcites →https://doi.org/10.1038/nri1182openalex-snapshot
DC-SIGN: escape mechanism for pathogens
inferredcites →https://doi.org/10.1038/nsmb784openalex-snapshot
Structural basis for distinct ligand-binding and targeting properties of the receptors DC-SIGN and DC-SIGNR
inferredcites →https://doi.org/10.1046/j.1537-2995.1998.38698326338.xopenalex-snapshot
Distribution of HIV type 1 (HIV‐1) in blood components: detection and significance of high levels of HIV‐1 associated with platelets
inferredcites →https://doi.org/10.1054/blre.2001.0188openalex-snapshot
HIV-related thrombocytopenia
inferredcites →https://doi.org/10.1073/pnas.032654399openalex-snapshot
Rhesus macaque dendritic cells efficiently transmit primate lentiviruses independently of DC-SIGN
inferredcites →https://doi.org/10.1073/pnas.051631398openalex-snapshot
DC-SIGNR, a DC-SIGN homologue expressed in endothelial cells, binds to human and simian immunodeficiency viruses and activates infection in trans
inferredcites →https://doi.org/10.1073/pnas.0831128100openalex-snapshot
L-SIGN (CD 209L) is a liver-specific capture receptor for hepatitis C virus
inferredcites →https://doi.org/10.1073/pnas.89.5.1582openalex-snapshot
Primary cultures of endothelial cells from the human liver sinusoid are permissive for human immunodeficiency virus type 1.
inferredcites →https://doi.org/10.1074/jbc.m301284200openalex-snapshot
DC-SIGN and L-SIGN Are High Affinity Binding Receptors for Hepatitis C Virus Glycoprotein E2
inferredcites →https://doi.org/10.1084/jem.20022212openalex-snapshot
Blockade of Attachment and Fusion Receptors Inhibits HIV-1 Infection of Human Cervical Tissue
inferredcites →https://doi.org/10.1084/jem.20030648openalex-snapshot
HIV-1 Cell to Cell Transfer across an Env-induced, Actin-dependent Synapse
inferredcites →https://doi.org/10.1086/423209openalex-snapshot
Analysis of Genetic Polymorphisms in CCR5, CCR2, Stromal Cell–Derived Factor–1, RANTES, and Dendritic Cell–Specific Intercellular Adhesion Molecule–3–Grabbing Nonintegrin in Seronegative Individuals Repeatedly Exposed to HIV‐1
inferredcites →https://doi.org/10.1089/088922202753472838openalex-snapshot
Cellular Factors Influence the Binding of HIV Type 1 to Cells
inferredcites →https://doi.org/10.1099/vir.0.80852-0openalex-snapshot
Infection of mature dendritic cells with herpes simplex virus type 1 dramatically reduces lymphoid chemokine-mediated migration
inferredcites →https://doi.org/10.1111/j.1365-2249.1992.tb03066.xopenalex-snapshot
During HIV-1 infection most blood dendritic cells are not productively infected and can induce allogeneic CD4+ T cells clonal expansion
inferredcites →https://doi.org/10.1111/j.1538-7836.2006.01749.xopenalex-snapshot
Lentivirus degradation and DC‐SIGN expression by human platelets and megakaryocytes
inferredcites →https://doi.org/10.1111/j.1600-0854.2004.00209.xopenalex-snapshot
Retroviral Spread by Induction of Virological Synapses
inferredcites →https://doi.org/10.1126/science.1084238openalex-snapshot
Recruitment of HIV and Its Receptors to Dendritic Cell-T Cell Junctions
inferredcites →https://doi.org/10.1126/science.1352913openalex-snapshot
Dendritic Cells Exposed to Human Immunodeficiency Virus Type-1 Transmit a Vigorous Cytopathic Infection to CD4 + T Cells
inferredcites →https://doi.org/10.1128/jvi.74.18.8550-8557.2000openalex-snapshot
CD4-Negative Cells Bind Human Immunodeficiency Virus Type 1 and Efficiently Transfer Virus to T Cells
inferredcites →https://doi.org/10.1128/jvi.74.21.10074-10080.2000openalex-snapshot
Human Immunodeficiency Virus Type 1 Spinoculation Enhances Infection through Virus Binding
inferredcites →https://doi.org/10.1128/jvi.75.10.4664-4672.2001openalex-snapshot
DC-SIGN Interactions with Human Immunodeficiency Virus Type 1 and 2 and Simian Immunodeficiency Virus
inferredcites →https://doi.org/10.1128/jvi.75.21.10281-10289.2001openalex-snapshot
Functional and Antigenic Characterization of Human, Rhesus Macaque, Pigtailed Macaque, and Murine DC-SIGN
inferredcites →https://doi.org/10.1128/jvi.75.21.10523-10526.2001openalex-snapshot
DC-SIGN Interactions with Human Immunodeficiency Virus: Virus Binding and Transfer Are Dissociable Functions
inferredcites →https://doi.org/10.1128/jvi.76.12.5905-5914.2002openalex-snapshot
Functional Evaluation of DC-SIGN Monoclonal Antibodies Reveals DC-SIGN Interactions with ICAM-3 Do Not Promote Human Immunodeficiency Virus Type 1 Transmission
inferredcites →https://doi.org/10.1128/jvi.76.18.9135-9142.2002openalex-snapshot
Quantitative Expression and Virus Transmission Analysis of DC-SIGN on Monocyte-Derived Dendritic Cells
inferredcites →https://doi.org/10.1128/jvi.76.4.1866-1875.2002openalex-snapshot
Expression of DC-SIGN by Dendritic Cells of Intestinal and Genital Mucosae in Humans and Rhesus Macaques
inferredcites →https://doi.org/10.1128/jvi.77.2.989-998.2003openalex-snapshot
Increased Mucosal Transmission but Not Enhanced Pathogenicity of the CCR5-Tropic, Simian AIDS-Inducing Simian/Human Immunodeficiency Virus SHIV SF162P3 Maps to Envelope gp120
inferredcites →https://doi.org/10.1128/jvi.77.23.12865-12874.2003openalex-snapshot
Binding of Human Immunodeficiency Virus Type 1 to Immature Dendritic Cells Can Occur Independently of DC-SIGN and Mannose Binding C-Type Lectin Receptors via a Cholesterol-Dependent Pathway
inferredcites →https://doi.org/10.1128/jvi.77.7.4070-4080.2003openalex-snapshot
Hepatitis C Virus Glycoproteins Interact with DC-SIGN and DC-SIGNR
inferredcites →https://doi.org/10.1128/jvi.78.20.10848-10855.2004openalex-snapshot
Lentivirus-Mediated RNA Interference of DC-SIGN Expression Inhibits Human Immunodeficiency Virus Transmission from Dendritic Cells to T Cells
inferredcites →https://doi.org/10.1128/jvi.78.24.14053-14056.2004openalex-snapshot
Association of DC-SIGN Promoter Polymorphism with Increased Risk for Parenteral, but Not Mucosal, Acquisition of Human Immunodeficiency Virus Type 1 Infection
inferredcites →https://doi.org/10.1128/jvi.79.11.6577-6587.2005openalex-snapshot
Plunder and Stowaways: Incorporation of Cellular Proteins by Enveloped Viruses
inferredcites →https://doi.org/10.1128/jvi.79.9.5386-5399.2005openalex-snapshot
Covert Human Immunodeficiency Virus Replication in Dendritic Cells and in DC-SIGN-Expressing Cells Promotes Long-Term Transmission to Lymphocytes
inferredcites →https://doi.org/10.1139/y94-043openalex-snapshot
Role of platelets in thrombosis and hemostasis
inferredcites →https://doi.org/10.1182/blood-2001-12-0191openalex-snapshot
Host defense role of platelets: engulfment of HIV andStaphylococcus aureus occurs in a specific subcellular compartment and is enhanced by platelet activation
inferredcites →https://doi.org/10.1182/blood-2003-09-3129openalex-snapshot
Immunodeficiency virus uptake, turnover, and 2-phase transfer in human dendritic cells
inferredcites →https://doi.org/10.1182/blood-2005-05-1994openalex-snapshot
A novel Syk-dependent mechanism of platelet activation by the C-type lectin receptor CLEC-2
inferredcites →https://doi.org/10.1182/blood.v75.10.1920.1920openalex-snapshot
Internalization of human immunodeficiency virus type I and other retroviruses by megakaryocytes and platelets
inferredcites →https://doi.org/10.1182/blood.v80.1.162.162openalex-snapshot
Presence of cross-reactive antibody between human immunodeficiency virus (HIV) and platelet glycoproteins in HIV-related immune thrombocytopenic purpura
inferredcites →https://doi.org/10.1182/blood.v91.4.1225openalex-snapshot
Productive Human Immunodeficiency Virus-1 Infection of Purified Megakaryocytic Progenitors/Precursors and Maturing Megakaryocytes
inferredcites →https://doi.org/10.1189/jlb.71.3.445openalex-snapshot
Constitutive and induced expression of DC-SIGN on dendritic cell and macrophage subpopulations in situ and in vitro
inferredcites →https://doi.org/10.1517/14728222.6.4.423openalex-snapshot
The role of DC-SIGN and DC-SIGNR in HIV and Ebola virus infection: can potential therapeutics block virus transmission and dissemination?
inferredcites →https://doi.org/10.2174/156801605774322364openalex-snapshot
Thrombocytopenia in HIV Disease: Clinical Relevance, Physiopathology and Management
inferredcites →https://doi.org/10.4049/jimmunol.175.7.4265openalex-snapshot
Dendritic Cell-Specific Intercellular Adhesion Molecule 3-Grabbing Nonintegrin/CD209 Is Abundant on Macrophages in the Normal Human Lymph Node and Is Not Required for Dendritic Cell Stimulation of the Mixed Leukocyte Reaction

What points at this work

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

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Platelets and Their Interactions with Other Immune Cells
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Platelets and Their Interactions with Other Immune Cells
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Tissue dendritic cells as portals for HIV entry
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Platelet CLEC‐2 and lung development
inferred← citeshttps://doi.org/10.1002/rth2.12710openalex-snapshot
Clustering extent‐dependent differential signaling by CLEC‐2 receptors in platelets
inferred← citeshttps://doi.org/10.1007/978-1-4419-0461-4_570openalex-snapshot
CLEC-2
inferred← citeshttps://doi.org/10.1007/978-1-4614-6438-9_570-1openalex-snapshot
CLEC-2
inferred← citeshttps://doi.org/10.1007/978-1-4614-7651-1_7openalex-snapshot
Cellular Entry of Retroviruses
inferred← citeshttps://doi.org/10.1007/978-3-031-96340-7_14openalex-snapshot
Platelet CLEC-2
inferred← citeshttps://doi.org/10.1007/978-3-031-96352-0_17openalex-snapshot
Platelets in Viral Pathophysiology
inferred← citeshttps://doi.org/10.1007/978-3-319-47462-5_10openalex-snapshot
The Role of CLEC-2 in and Beyond the Vasculature
inferred← citeshttps://doi.org/10.1007/978-3-319-47462-5_34openalex-snapshot
Platelets and Immunity
inferred← citeshttps://doi.org/10.1007/978-3-319-47462-5_72openalex-snapshot
Virus–Platelet Associations
inferred← citeshttps://doi.org/10.1007/978-3-319-67199-4_570openalex-snapshot
CLEC-2
inferred← citeshttps://doi.org/10.1007/978-3-7091-1065-2_34openalex-snapshot
Dectin-1 Receptor Family
inferred← citeshttps://doi.org/10.1007/978-3-7091-1646-3_8openalex-snapshot
Platelets in Lymph Vessel Development and Integrity
inferred← citeshttps://doi.org/10.1007/978-3-7643-7783-0_3openalex-snapshot
Attachment of human immunodeficiency virus to cells and its inhibition
inferred← citeshttps://doi.org/10.1007/978-4-431-56015-9_6openalex-snapshot
C-Type Lectin-Like Receptor 2 (CLEC-2)
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The Biologic Activity of Aggretin/Rhodocytin, a Snake Venom C-Type Lectin Protein (Snaclec)
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Platelets and viruses: an ambivalent relationship
inferred← citeshttps://doi.org/10.1007/s00281-011-0286-4openalex-snapshot
Platelets: versatile effector cells in hemostasis, inflammation, and the immune continuum
inferred← citeshttps://doi.org/10.1007/s10719-012-9413-2openalex-snapshot
The production of soluble C-type lectin-like receptor 2 is a regulated process
inferred← citeshttps://doi.org/10.1007/s10719-012-9419-9openalex-snapshot
The C-type lectin-like receptors of Dectin-1 cluster in natural killer gene complex
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Dengue virus infection: how platelet-leukocyte crosstalk shapes thrombotic events and inflammation
inferred← citeshttps://doi.org/10.1007/s11684-015-0424-9openalex-snapshot
Emerging roles of podoplanin in vascular development and homeostasis
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COVID-19 vaccines adverse events: potential molecular mechanisms
inferred← citeshttps://doi.org/10.1007/s12185-019-02680-4openalex-snapshot
Soluble CLEC-2 is generated independently of ADAM10 and is increased in plasma in acute coronary syndrome: comparison with soluble GPVI
inferred← citeshttps://doi.org/10.1007/s15010-026-02838-3openalex-snapshot
Viral subversion of megakaryopoiesis: reshaping the landscapes of immune regulation
inferred← citeshttps://doi.org/10.1016/b978-0-12-374546-0.00028-6openalex-snapshot
Lectin-like interactions in virus–cell recognition
inferred← citeshttps://doi.org/10.1016/b978-0-12-387837-3.00009-2openalex-snapshot
Platelet Receptors
inferred← citeshttps://doi.org/10.1016/b978-0-12-387837-3.00011-0openalex-snapshot
GPVI and CLEC-2
inferred← citeshttps://doi.org/10.1016/b978-0-12-387837-3.00036-5openalex-snapshot
Inflammation
inferred← citeshttps://doi.org/10.1016/b978-0-12-813456-6.00009-6openalex-snapshot
Platelet Receptors
inferred← citeshttps://doi.org/10.1016/bs.ai.2022.09.001openalex-snapshot
Self-referential immune recognition through C-type lectin receptors
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Platelets and inter-cellular communication in immune responses: Dialogue with both professional and non-professional immune cells
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The Evolution of HIV-1 Interactions with Coreceptors and Mannose C-Type Lectin Receptors
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Platelet C-Type Lectin-Like Receptor 2 Reduces Cholestatic Liver Injury in Mice
inferred← citeshttps://doi.org/10.1016/j.bbrc.2008.03.070openalex-snapshot
Molecular characterization of two novel isoforms and a soluble form of mouse CLEC-2
inferred← citeshttps://doi.org/10.1016/j.bbrc.2009.09.087openalex-snapshot
RACK1 associates with CLEC-2 and promotes its ubiquitin–proteasome degradation
inferred← citeshttps://doi.org/10.1016/j.bcp.2015.02.004openalex-snapshot
Impact of the PI3-kinase/Akt pathway on ITAM and hemITAM receptors: Haemostasis, platelet activation and antithrombotic therapy
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SARS-CoV-2 S1 protein induces IgG-mediated platelet activation and is prevented by 1.8-cineole
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Should studies on Glanzmann thrombasthenia not be telling us more about cardiovascular disease and other major illnesses?
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Regulation of cytoskeleton and adhesion signaling in osteoclasts by tetraspanin CD82
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Elucidation of differences in N-glycosylation between different molecular weight forms of recombinant CLEC-2 by LC MALDI tandem MS
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Higher plasma C-type lectin-like receptor 2 concentrations for prediction of higher risk of 30-day mortality in isolated severe blunt traumatic brain injury
inferred← citeshttps://doi.org/10.1016/j.cellsig.2016.07.007openalex-snapshot
E3 ubiquitin ligase CHIP interacts with C-type lectin-like receptor CLEC-2 and promotes its ubiquitin-proteasome degradation
inferred← citeshttps://doi.org/10.1016/j.coph.2008.11.001openalex-snapshot
Thrombomodulation via CLEC-2 targeting
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HIV and SIV associated thrombocytopenia: an expanding role for platelets in the pathogenesis of HIV
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Platelet Factor 4 Promotes Rapid Replication and Propagation of Dengue and Japanese Encephalitis Viruses
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Morphometric image analysis of placental C-type lectin domain family 2, member D (CLEC2D) immuno-expression in HIV associated pre-eclampsia
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Regulation of platelet function by natural bioactive compounds
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High glucose disrupts oligosaccharide recognition function via competitive inhibition: A potential mechanism for immune dysregulation in diabetes mellitus
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Inhibitory C-type lectin receptors in myeloid cells
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Myeloid C-type Lectin Receptors in Pathogen Recognition and Host Defense
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Myeloid C-type lectin receptors in innate immune recognition
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Platelets: Orchestrators of immunity in host defense and beyond
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Platelet’s plea to Immunologists: Please do not forget me
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Differential platelet receptor expression for viral capture (DC-SIGN) and plasma leakage in patients with dengue infection
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Inhibition of cellular activation induced by platelet factor 4 via the CXCR3 pathway ameliorates Japanese encephalitis and dengue viral infections
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Viral coagulation: pushing the envelope
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Platelets to surrogate lung inflammation in COVID-19 patients
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Platelets immune response against Mycobacterium tuberculosis infection
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In vitro and in vivo metabolic tagging and modulation of platelets
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Abnormalities in C-type lectin-like receptor 2 in a patient with Gorham-Stout disease: the first case report
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Beyond hemostasis, the immunomodulatory nature of platelets
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A Platform of C-type Lectin-like Receptor CLEC-2 for Binding O-Glycosylated Podoplanin and Nonglycosylated Rhodocytin
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Step up to the platelet: Role of platelets in inflammation and infection
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The Immune Nature of Platelets Revisited
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Immunologie plaquettaire et réponse immune
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Plaquettes sanguines, réponses aux signaux de danger infectieux et inflammation : vers un nouveau paradigme ?
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Modulation of HIV and SIV neutralization sensitivity by DC-SIGN and mannose-binding lectin
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Interactions of LSECtin and DC-SIGN/DC-SIGNR with viral ligands: Differential pH dependence, internalization and virion binding
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The Crystal Structure of the Platelet Activator Aggretin Reveals a Novel (αβ)2Dimeric Structure
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CLEC-2
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Signalling through C-type lectin receptors: shaping immune responses
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The non-haemostatic role of platelets in systemic lupus erythematosus
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Platelets in pediatric and neonatal sepsis: novel mediators of the inflammatory cascade
inferred← citeshttps://doi.org/10.1038/s41467-019-10360-4openalex-snapshot
Extracellular vesicles from CLEC2-activated platelets enhance dengue virus-induced lethality via CLEC5A/TLR2
inferred← citeshttps://doi.org/10.1038/s41598-018-33403-0openalex-snapshot
Persistent platelet activation and apoptosis in virologically suppressed HIV-infected individuals
inferred← citeshttps://doi.org/10.1038/s41598-021-94307-0openalex-snapshot
Characterization and visualization of murine coagulation factor VIII-producing cells in vivo
inferred← citeshttps://doi.org/10.1039/d2cs00954dopenalex-snapshot
Glycomimetics for the inhibition and modulation of lectins
inferred← citeshttps://doi.org/10.1042/bj20071216openalex-snapshot
Renal cells activate the platelet receptor CLEC-2 through podoplanin
inferred← citeshttps://doi.org/10.1042/cs20220039openalex-snapshot
Casting a wide NET: an update on uncontrolled NETosis in response to COVID-19 infection
inferred← citeshttps://doi.org/10.1051/medsci/2021006openalex-snapshot
Un passager clandestin
inferred← citeshttps://doi.org/10.1055/a-2523-1821openalex-snapshot
Recent Advances in Immunothrombosis and Thromboinflammation
inferred← citeshttps://doi.org/10.1055/a-2731-2399openalex-snapshot
Platelets in Neonatal Sepsis: Beyond Clotting, from Silent Players to Immune Orchestrators
inferred← citeshttps://doi.org/10.1055/s-0037-1604090openalex-snapshot
Platelet CLEC-2: Roles Beyond Hemostasis
inferred← citeshttps://doi.org/10.1055/s-0037-1619045openalex-snapshot
Arterial thrombus formation
inferred← citeshttps://doi.org/10.1055/s-0040-1708827openalex-snapshot
A Champion of Host Defense: A Generic Large-Scale Cause for Platelet Dysfunction and Depletion in Infection
inferred← citeshttps://doi.org/10.1055/s-0041-1726033openalex-snapshot
Platelet Function in Viral Immunity and SARS-CoV-2 Infection
inferred← citeshttps://doi.org/10.1055/s-0044-1791512openalex-snapshot
Modulating Immune Responses: The Double-Edged Sword of Platelet CD40L
inferred← citeshttps://doi.org/10.1073/pnas.1207314109openalex-snapshot
Identification of the platelet-derived chemokine CXCL4/PF-4 as a broad-spectrum HIV-1 inhibitor
inferred← citeshttps://doi.org/10.1074/jbc.m111.329987openalex-snapshot
Platelet Activation Receptor CLEC-2 Regulates Blood/Lymphatic Vessel Separation by Inhibiting Proliferation, Migration, and Tube Formation of Lymphatic Endothelial Cells
inferred← citeshttps://doi.org/10.1074/jbc.m117.791012openalex-snapshot
Gq pathway regulates proximal C-type lectin-like receptor-2 (CLEC-2) signaling in platelets
inferred← citeshttps://doi.org/10.1074/jbc.m609558200openalex-snapshot
The C-type Lectin Receptors CLEC-2 and Dectin-1, but Not DC-SIGN, Signal via a Novel YXXL-dependent Signaling Cascade
inferred← citeshttps://doi.org/10.1074/jbc.m610383200openalex-snapshot
The Crystal Structure and Mutational Binding Analysis of the Extracellular Domain of the Platelet-activating Receptor CLEC-2
inferred← citeshttps://doi.org/10.1080/08830185.2017.1309528openalex-snapshot
Multiple functions of the E3 ubiquitin ligase CHIP in immunity
inferred← citeshttps://doi.org/10.1080/09537104.2018.1478401openalex-snapshot
Roles of the CLEC-2–podoplanin interaction in tumor progression
inferred← citeshttps://doi.org/10.1080/09537104.2020.1718631openalex-snapshot
Platelets and extracellular traps in infections
inferred← citeshttps://doi.org/10.1080/09537104.2020.1849606openalex-snapshot
Hiding in plain sight – platelets, the silent carriers of HIV-1
inferred← citeshttps://doi.org/10.1080/09537104.2021.1887842openalex-snapshot
Platelets and viruses
inferred← citeshttps://doi.org/10.1080/09537104.2021.1945571openalex-snapshot
Platelet activation by charged ligands and nanoparticles: platelet glycoprotein receptors as pattern recognition receptors
inferred← citeshttps://doi.org/10.1080/09537104.2021.1952179openalex-snapshot
Platelet–leukocyte interactions in the pathogenesis of viral infections
inferred← citeshttps://doi.org/10.1080/10408363.2016.1200008openalex-snapshot
Platelets are versatile cells: New discoveries in hemostasis, thrombosis, immune responses, tumor metastasis and beyond
inferred← citeshttps://doi.org/10.1086/520607openalex-snapshot
Analysis of the Interaction of Ebola Virus Glycoprotein with DC‐SIGN (Dendritic Cell–Specific Intercellular Adhesion Molecule 3–Grabbing Nonintegrin) and Its Homologue DC‐SIGNR
inferred← citeshttps://doi.org/10.1086/588710openalex-snapshot
Protective Role of DC‐SIGN(CD209)Neck‐Region Alleles with <5 Repeat Units in HIV‐1 Transmission
inferred← citeshttps://doi.org/10.1089/aid.2006.0311openalex-snapshot
Platelet Count Is Associated with Plasma HIV Type 1 RNA and Disease Progression
inferred← citeshttps://doi.org/10.1089/vim.2021.0135openalex-snapshot
Dengue Virus and Platelets: From the Biology to the Clinic
inferred← citeshttps://doi.org/10.1093/glycob/cwz097openalex-snapshot
Fucoidan suppresses the gastric cancer cell malignant phenotype and production of TGF-β1 via CLEC-2
inferred← citeshttps://doi.org/10.1093/jb/mvr079openalex-snapshot
Essential in vivo roles of the platelet activation receptor CLEC-2 in tumour metastasis, lymphangiogenesis and thrombus formation
inferred← citeshttps://doi.org/10.1093/jimmun/vkag197openalex-snapshot
Platelets are essential for survival of respiratory-restricted viral infection
inferred← citeshttps://doi.org/10.1093/jleuko/qiae048openalex-snapshot
Increased platelet–CD8+ T-cell aggregates displaying high activation, exhaustion, and tendency to death correlate with disease progression in people with HIV-1
inferred← citeshttps://doi.org/10.1097/coh.0b013e328356e9f3openalex-snapshot
Use of (alternative) coreceptors for HIV entry
inferred← citeshttps://doi.org/10.1097/moh.0b013e3283497dfbopenalex-snapshot
Recently recognized platelet agonists
inferred← citeshttps://doi.org/10.1097/qad.0b013e328336098copenalex-snapshot
Platelet function and HIV: a case–control study
inferred← citeshttps://doi.org/10.1099/acmi.0.000481.v3openalex-snapshot
Binding of respiratory syncytial virus particles to platelets does not result in their degranulation in vitro
inferred← citeshttps://doi.org/10.1100/2012/931386openalex-snapshot
Evolution of the C-Type Lectin-Like Receptor Genes of the DECTIN-1 Cluster in the NK Gene Complex
inferred← citeshttps://doi.org/10.1111/1348-0421.13211openalex-snapshot
Classification of C‐Type Lectins and Recognition of Pathogens
inferred← citeshttps://doi.org/10.1111/1574-6976.12052openalex-snapshot
Bitter-sweet symphony: glycan–lectin interactions in virus biology
inferred← citeshttps://doi.org/10.1111/acel.13749openalex-snapshot
Platelet response to influenza vaccination reflects effects of aging
inferred← citeshttps://doi.org/10.1111/ejh.13705openalex-snapshot
T cell–mediated autoimmunity in immune thrombocytopenia
inferred← citeshttps://doi.org/10.1111/ijlh.12307openalex-snapshot
The evaluation of platelet indices and markers of inflammation, coagulation and disease progression in treatment‐naïve, asymptomatic HIV ‐infected individuals
inferred← citeshttps://doi.org/10.1111/j.0105-2896.2009.00882.xopenalex-snapshot
Syk‐coupled C‐type lectin receptors that mediate cellular activation via single tyrosine based activation motifs
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2009.03372.xopenalex-snapshot
Novel interactions in platelet biology: CLEC-2/podoplanin and laminin/GPVI
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2010.03875.xopenalex-snapshot
GPVI and CLEC‐2 in hemostasis and vascular integrity
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2011.04335.xopenalex-snapshot
Novel platelet activation receptor CLEC‐2: from discovery to prospects
inferred← citeshttps://doi.org/10.1111/j.1538-7836.2011.04356.xopenalex-snapshot
Historical perspective and future directions in platelet research
inferred← citeshttps://doi.org/10.1111/j.1574-6968.2008.01418.xopenalex-snapshot
The fungal pattern recognition receptor, Dectin-1, and the associated cluster of C-type lectin-like receptors
inferred← citeshttps://doi.org/10.1111/jth.12235openalex-snapshot
Platelet receptors activated via mulitmerization: glycoprotein VI, GPIb‐IX‐V, and CLEC‐2
inferred← citeshttps://doi.org/10.1111/jth.13590openalex-snapshot
Physiologic and pathophysiologic roles of interaction between C‐type lectin‐like receptor 2 and podoplanin: partners from in utero to adulthood
inferred← citeshttps://doi.org/10.1111/jth.13669openalex-snapshot
Targeting of C‐type lectin‐like receptor 2 or P2Y12 for the prevention of platelet activation by immunotherapeutic CpG oligodeoxynucleotides
inferred← citeshttps://doi.org/10.1111/mmi.14837openalex-snapshot
Fc‐conjugated C‐type lectin receptors: Tools for understanding host–pathogen interactions
inferred← citeshttps://doi.org/10.1126/scitranslmed.aat6263openalex-snapshot
Platelets from HIV-infected individuals on antiretroviral drug therapy with poor CD4 + T cell recovery can harbor replication-competent HIV despite viral suppression
inferred← citeshttps://doi.org/10.1128/jvi.00554-10openalex-snapshot
A Single Asparagine-Linked Glycosylation Site of the Severe Acute Respiratory Syndrome Coronavirus Spike Glycoprotein Facilitates Inhibition by Mannose-Binding Lectin through Multiple Mechanisms
inferred← citeshttps://doi.org/10.11406/rinketsu.50.389openalex-snapshot
新規血小板活性化受容体CLEC-2とその生体内リガンド, ポドプラニン
inferred← citeshttps://doi.org/10.1152/ajprenal.00629.2009openalex-snapshot
DC-specific ICAM-3-grabbing nonintegrin mediates internalization of HIV-1 into human podocytes
inferred← citeshttps://doi.org/10.1155/2013/869718openalex-snapshot
Targeting Antigens to Dendritic Cell Receptors for Vaccine Development
inferred← citeshttps://doi.org/10.1160/th13-04-0341openalex-snapshot
Platelet chemokines in health and disease
inferred← citeshttps://doi.org/10.1160/ths10-11-0720openalex-snapshot
Platelets, inflammation and tissue regeneration
inferred← citeshttps://doi.org/10.1161/01.res.0000252802.25497.b7openalex-snapshot
Platelets as Immune Cells
inferred← citeshttps://doi.org/10.1161/atvbaha.120.314180openalex-snapshot
Platelets Endocytose Viral Particles and Are Activated via TLR (Toll-Like Receptor) Signaling
inferred← citeshttps://doi.org/10.1161/atvbaha.120.314645openalex-snapshot
Role of Platelets in Detection and Regulation of Infection
inferred← citeshttps://doi.org/10.1161/circresaha.121.319821openalex-snapshot
Platelet and Megakaryocyte Roles in Innate and Adaptive Immunity
inferred← citeshttps://doi.org/10.1161/circresaha.122.321930openalex-snapshot
Platelets and SARS-CoV-2 During COVID-19: Immunity, Thrombosis, and Beyond
inferred← citeshttps://doi.org/10.1172/jci122955openalex-snapshot
Functional significance of the platelet immune receptors GPVI and CLEC-2
inferred← citeshttps://doi.org/10.1177/08892229251365583openalex-snapshot
Analysis of Factors Influencing Immunological Failure in Elderly People Living with HIV Undergoing Antiretroviral Therapy: A LASSO-Logistic Regression Approach
inferred← citeshttps://doi.org/10.1182/asheducation-2016.1.256openalex-snapshot
Platelets in infectious disease
inferred← citeshttps://doi.org/10.1182/blood-2009-05-222273openalex-snapshot
CLEC-2 is an essential platelet-activating receptor in hemostasis and thrombosis
inferred← citeshttps://doi.org/10.1182/blood-2012-09-456004openalex-snapshot
A detailed proteomic analysis of rhodocytin-activated platelets reveals novel clues on the CLEC-2 signalosome: implications for CLEC-2 signaling regulation
inferred← citeshttps://doi.org/10.1182/blood-2014-05-572818openalex-snapshot
CLEC-2 expression is maintained on activated platelets and on platelet microparticles
inferred← citeshttps://doi.org/10.1182/blood.2019003977openalex-snapshot
Aspirin and antiplatelet treatments in cancer
inferred← citeshttps://doi.org/10.1182/bloodadvances.2018016261openalex-snapshot
Cobalt hematoporphyrin inhibits CLEC-2–podoplanin interaction, tumor metastasis, and arterial/venous thrombosis in mice
inferred← citeshttps://doi.org/10.1182/bloodadvances.2020001698openalex-snapshot
Heme activates platelets and exacerbates rhabdomyolysis-induced acute kidney injury via CLEC-2 and GPVI/FcRγ
inferred← citeshttps://doi.org/10.1182/bloodadvances.2020002420openalex-snapshot
Platelets function as an acute viral reservoir during HIV-1 infection by harboring virus and T-cell complex formation
inferred← citeshttps://doi.org/10.1182/bloodadvances.2022007444openalex-snapshot
Platelet activation by SARS-CoV-2 implicates the release of active tissue factor by infected cells
inferred← citeshttps://doi.org/10.1183/16000617.0062-2021openalex-snapshot
Platelets: a potential role in chronic respiratory diseases?
inferred← citeshttps://doi.org/10.1186/1742-4690-10-48openalex-snapshot
Platelet activation suppresses HIV-1 infection of T cells
inferred← citeshttps://doi.org/10.1186/1742-4690-7-47openalex-snapshot
Incorporation of podoplanin into HIV released from HEK-293T cells, but not PBMC, is required for efficient binding to the attachment factor CLEC-2
inferred← citeshttps://doi.org/10.1186/s12865-015-0092-1openalex-snapshot
Human platelets and their capacity of binding viruses: meaning and challenges?
inferred← citeshttps://doi.org/10.1186/s12929-021-00741-7openalex-snapshot
C-type lectins and extracellular vesicles in virus-induced NETosis
inferred← citeshttps://doi.org/10.1186/s12959-018-0170-8openalex-snapshot
Human blood platelets and viruses: defense mechanism and role in the removal of viral pathogens
inferred← citeshttps://doi.org/10.1186/s12959-021-00311-9openalex-snapshot
Thrombosis in COVID-19 infection: Role of platelet activation-mediated immunity
inferred← citeshttps://doi.org/10.1186/s12967-025-06591-3openalex-snapshot
Over-activation and dysfunction of platelet-NK cell aggregates in HIV-infected individuals
inferred← citeshttps://doi.org/10.1186/s13045-020-00954-7openalex-snapshot
SARS-CoV-2 binds platelet ACE2 to enhance thrombosis in COVID-19
inferred← citeshttps://doi.org/10.1189/jlb.1206753openalex-snapshot
The role of the β-glucan receptor Dectin-1 in control of fungal infection
inferred← citeshttps://doi.org/10.1371/journal.pntd.0002858openalex-snapshot
The Role of Platelets in the Pathogenesis of Viral Hemorrhagic Fevers
inferred← citeshttps://doi.org/10.1371/journal.pntd.0011488openalex-snapshot
Dabie bandavirus infection induces macrophagic pyroptosis and this process is attenuated by platelets
inferred← citeshttps://doi.org/10.1371/journal.pone.0013139openalex-snapshot
Inference of Surface Membrane Factors of HIV-1 Infection through Functional Interaction Networks
inferred← citeshttps://doi.org/10.1371/journal.pone.0071051openalex-snapshot
Transcriptome Analysis of Duck Liver and Identification of Differentially Expressed Transcripts in Response to Duck Hepatitis A Virus Genotype C Infection
inferred← citeshttps://doi.org/10.1371/journal.pone.0081002openalex-snapshot
Platelets and Erythrocyte-Bound Platelets Bind Infectious HIV-1 in Plasma of Chronically Infected Patients
inferred← citeshttps://doi.org/10.1371/journal.pone.0130061openalex-snapshot
Platelet Activation in Human Immunodeficiency Virus Type-1 Patients Is Not Altered with Cocaine Abuse
inferred← citeshttps://doi.org/10.1371/journal.pone.0194185openalex-snapshot
HIV induces production of IL-18 from intestinal epithelial cells that increases intestinal permeability and microbial translocation
inferred← citeshttps://doi.org/10.1371/journal.pone.0206346openalex-snapshot
Dynamic modulation of DC-SIGN and FcΥR2A receptors expression on platelets in dengue
inferred← citeshttps://doi.org/10.1371/journal.ppat.1012190openalex-snapshot
Macrophage- and CD4+ T cell-derived SIV differ in glycosylation, infectivity and neutralization sensitivity
inferred← citeshttps://doi.org/10.1371/journal.ppat.1013985openalex-snapshot
Platelet-like particles released from Ebola virus-infected megakaryocytic cells behave like virus-like particles
inferred← citeshttps://doi.org/10.15252/emmm.202216351openalex-snapshot
Inhibition of SARS‐CoV‐2‐mediated thromboinflammation by CLEC2.Fc
inferred← citeshttps://doi.org/10.1529/biophysj.107.106708openalex-snapshot
Stochastic Entry of Enveloped Viruses: Fusion versus Endocytosis
inferred← citeshttps://doi.org/10.1590/0037-8682-0105-2016openalex-snapshot
Human platelets antigens influence the viral load of platelets after the interaction of the platelets with HCV and HIV in vitro
inferred← citeshttps://doi.org/10.17305/bb.2023.10135openalex-snapshot
The role of platelets in sepsis: A review
inferred← citeshttps://doi.org/10.17749/2313-7347/ob.gyn.rep.2022.305openalex-snapshot
The role of platelets in antiviral immunity
inferred← citeshttps://doi.org/10.2147/jbm.s365218openalex-snapshot
Haematological Traits in Symptomatic and Asymptomatic COVID-19 Positive Patients for Predicting Severity and Hospitalization
inferred← citeshttps://doi.org/10.2174/187152810793937991openalex-snapshot
Platelet Toll-Like Receptor Expression: The Link Between “Danger” Ligands and Inflammation
inferred← citeshttps://doi.org/10.2174/187152908784533739openalex-snapshot
Beyond Hemostasis: The Role of Platelets in Inflammation, Malignancy and Infection
inferred← citeshttps://doi.org/10.21873/invivo.13766openalex-snapshot
Hyperexpression ofPTAFRandPF4as Possible Platelet Risk Biomarkers in Patients With COVID-19
inferred← citeshttps://doi.org/10.2217/fmb.13.104openalex-snapshot
Platelets as Immune Cells in Infectious Diseases
inferred← citeshttps://doi.org/10.24287/1726-1708-2021-20-1-184-191openalex-snapshot
Platelets in COVID-19: “innocent by-standers” or active participants?
inferred← citeshttps://doi.org/10.2491/jjsth.20.401openalex-snapshot
An overview of the novel platelet activation receptor CLEC-2
inferred← citeshttps://doi.org/10.2491/jjsth.22.348openalex-snapshot
Novel platelet activation receptor CLEC-2
inferred← citeshttps://doi.org/10.2491/jjsth.23.259openalex-snapshot
A role of platelets in infection and inflammation
inferred← citeshttps://doi.org/10.2491/jjsth.26.29openalex-snapshot
C-type lectin receptors
inferred← citeshttps://doi.org/10.2491/jjsth.28.518openalex-snapshot
Identification of the platelet activation receptor CLEC-2, its endogenous ligand podoplanin, and pathophysiological roles of their interaction
inferred← citeshttps://doi.org/10.2491/jjsth.34.414openalex-snapshot
The platelet activation receptor CLEC-2: from basic research to prospect of clinical application
inferred← citeshttps://doi.org/10.25439/rmt.27589824openalex-snapshot
Investigating novel platelet immunoreceptor ‘CEACAM2’ in contact-dependent events that modulate platelet thrombus formation
inferred← citeshttps://doi.org/10.30607/kvj.1524672openalex-snapshot
Determination of Hematological Indices in Dogs with Acute CDV Infection
inferred← citeshttps://doi.org/10.3109/09537104.2011.556274openalex-snapshot
The novel platelet activation receptor CLEC-2
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