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Plasmodium falciparum growth is regulated by Sphingosine 1 phosphate produced by Host Erythrocyte Membrane Sphingosine kinase 1

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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/ijc.24222openalex-snapshot

Molecular imaging of glucose uptake in oral neoplasia following topical application of fluorescently labeled deoxy‐glucose

inferredcites →https://doi.org/10.1002/jcb.22507openalex-snapshot

Erythrocytes serve as a reservoir for cellular and extracellular sphingosine 1‐phosphate

inferredcites →https://doi.org/10.1006/bbrc.1997.7993openalex-snapshot

Identification of the First Mammalian Sphingosine Phosphate Lyase Gene and Its Functional Expression in Yeast

inferredcites →https://doi.org/10.1007/s11307-005-0011-6openalex-snapshot

Uptake of a Fluorescent Deoxyglucose Analog (2-NBDG) in Tumor Cells

inferredcites →https://doi.org/10.1016/j.abb.2009.09.013openalex-snapshot

Sphingosine kinase 1 localized to the plasma membrane lipid raft microdomain overcomes serum deprivation induced growth inhibition

inferredcites →https://doi.org/10.1016/j.celrep.2015.03.011openalex-snapshot

Genetic Investigation of Tricarboxylic Acid Metabolism during the Plasmodium falciparum Life Cycle

inferredcites →https://doi.org/10.1016/j.chom.2015.08.003openalex-snapshot

Profiling the Essential Nature of Lipid Metabolism in Asexual Blood and Gametocyte Stages of Plasmodium falciparum

inferredcites →https://doi.org/10.1016/j.febslet.2011.04.042openalex-snapshot

Drug‐resistant malaria: Molecular mechanisms and implications for public health

inferredcites →https://doi.org/10.1016/j.jbbm.2005.08.001openalex-snapshot

2-NBDG as a fluorescent indicator for direct glucose uptake measurement

inferredcites →https://doi.org/10.1016/j.jbior.2015.09.001openalex-snapshot

Role of sphingosine 1-phosphate receptors, sphingosine kinases and sphingosine in cancer and inflammation

inferredcites →https://doi.org/10.1016/j.molbiopara.2010.09.001openalex-snapshot

Central carbon metabolism of Plasmodium parasites

inferredcites →https://doi.org/10.1016/j.molcel.2012.04.033openalex-snapshot

The Sjögren-Larsson Syndrome Gene Encodes a Hexadecenal Dehydrogenase of the Sphingosine 1-Phosphate Degradation Pathway

inferredcites →https://doi.org/10.1016/j.tcb.2011.09.003openalex-snapshot

Sphingosine-1-phosphate signaling and its role in disease

inferredcites →https://doi.org/10.1016/j.tibs.2005.01.005openalex-snapshot

Multifaceted roles of glycolytic enzymes

inferredcites →https://doi.org/10.1016/j.vaccine.2012.02.037openalex-snapshot

Re-circulation of lymphocytes mediated by sphingosine-1-phosphate receptor-1 contributes to resistance against experimental infection with the protozoan parasite Trypanosoma cruzi

inferredcites →https://doi.org/10.1016/s0021-9258(18)82379-1openalex-snapshot

Regulation of glycolysis via reversible enzyme binding to the membrane protein, band 3

inferredcites →https://doi.org/10.1016/s0969-2126(97)00230-xopenalex-snapshot

Triosephosphate isomerase from Plasmodium falciparum:. the crystal structure provides insights into antimalarial drug design

inferredcites →https://doi.org/10.1021/jm030796nopenalex-snapshot

Isoquine and Related Amodiaquine Analogues: A New Generation of Improved 4-Aminoquinoline Antimalarials

inferredcites →https://doi.org/10.1038/nature07713openalex-snapshot

Sphingosine-1-phosphate mobilizes osteoclast precursors and regulates bone homeostasis

inferredcites →https://doi.org/10.1038/nature09128openalex-snapshot

Sphingosine-1-phosphate is a missing cofactor for the E3 ubiquitin ligase TRAF2

inferredcites →https://doi.org/10.1038/nature24053openalex-snapshot

Mfsd2b is essential for the sphingosine-1-phosphate export in erythrocytes and platelets

inferredcites →https://doi.org/10.1038/ncomms11388openalex-snapshot

Arabidopsis PROTEASOME REGULATOR1 is required for auxin-mediated suppression of proteasome activity and regulates auxin signalling

inferredcites →https://doi.org/10.1038/ncomms12086openalex-snapshot

Sphingosine-1-phosphate promotes erythrocyte glycolysis and oxygen release for adaptation to high-altitude hypoxia

inferredcites →https://doi.org/10.1038/ng.3189openalex-snapshot

Genetic architecture of artemisinin-resistant Plasmodium falciparum

inferredcites →https://doi.org/10.1054/drup.2000.0177openalex-snapshot

Glycolysis as a target for the design of new anti-trypanosome drugs

inferredcites →https://doi.org/10.1074/jbc.m502207200openalex-snapshot

SphK1 and SphK2, Sphingosine Kinase Isoenzymes with Opposing Functions in Sphingolipid Metabolism

inferredcites →https://doi.org/10.1074/jbc.m701641200openalex-snapshot

Protein Kinase D-mediated Phosphorylation and Nuclear Export of Sphingosine Kinase 2

inferredcites →https://doi.org/10.1074/jbc.m703329200openalex-snapshot

Recycling of Sphingosine Is Regulated by the Concerted Actions of Sphingosine-1-phosphate Phosphohydrolase 1 and Sphingosine Kinase 2

inferredcites →https://doi.org/10.1084/jem.20090525openalex-snapshot

T-bet–dependent S1P5 expression in NK cells promotes egress from lymph nodes and bone marrow

inferredcites →https://doi.org/10.1086/651562openalex-snapshot

High Heritability of Malaria Parasite Clearance Rate Indicates a Genetic Basis for Artemisinin Resistance in Western Cambodia

inferredcites →https://doi.org/10.1089/scd.2006.15.789openalex-snapshot

Mediation of Apoptosis and Proliferation of Human Embryonic Stem Cells by Sphingosine-1-Phosphate

inferredcites →https://doi.org/10.1093/intimm/dxz037openalex-snapshot

Sphingosine 1-phosphate and inflammation

inferredcites →https://doi.org/10.1096/fj.06-7433comopenalex-snapshot

Erythrocytes store and release sphingosine 1‐phosphate in blood

inferredcites →https://doi.org/10.1111/febs.13615openalex-snapshot

Targeting glycolysis in the malaria parasite Plasmodium falciparum

inferredcites →https://doi.org/10.1124/jpet.108.141929openalex-snapshot

The Inhibitory Effect of 2-Halo Derivatives of d-Glucose on Glycolysis and on the Proliferation of the Human Malaria Parasite Plasmodium falciparum

inferredcites →https://doi.org/10.1126/science.1139221openalex-snapshot

Promotion of Lymphocyte Egress into Blood and Lymph by Distinct Sources of Sphingosine-1-Phosphate

inferredcites →https://doi.org/10.1126/science.781840openalex-snapshot

Human Malaria Parasites in Continuous Culture

inferredcites →https://doi.org/10.1146/annurev.micro.51.1.97openalex-snapshot

HEMOGLOBIN METABOLISM IN THE MALARIA PARASITEPLASMODIUM FALCIPARUM

inferredcites →https://doi.org/10.1152/ajplung.00311.2002openalex-snapshot

Role of sphingosine-1 phosphate in the enhancement of endothelial barrier integrity by platelet-released products

inferredcites →https://doi.org/10.1158/0008-5472.can-07-2090openalex-snapshot

Involvement of Sphingosine Kinase 2 in p53-Independent Induction of p21 by the Chemotherapeutic Drug Doxorubicin

inferredcites →https://doi.org/10.1172/jci38575openalex-snapshot

Sphingosine-1-phosphate in the plasma compartment regulates basal and inflammation-induced vascular leak in mice

inferredcites →https://doi.org/10.1179/204777312x13305103762583openalex-snapshot

Identifying an essential interaction between malaria parasites and erythrocytes unlocks the door to promising vaccine targets

inferredcites →https://doi.org/10.1186/1475-2875-10-37openalex-snapshot

In vitro susceptibility to quinine and microsatellite variations of the Plasmodium falciparum Na+/H+ exchanger (Pfnhe-1) gene: the absence of association in clinical isolates from the Republic of Congo

inferredcites →https://doi.org/10.1186/1475-2875-6-121openalex-snapshot

World Antimalarial Resistance Network (WARN) III: Molecular markers for drug resistant malaria

inferredcites →https://doi.org/10.1186/s12936-016-1130-zopenalex-snapshot

Changes in lipid composition during sexual development of the malaria parasite Plasmodium falciparum

inferredcites →https://doi.org/10.1194/jlr.d001503openalex-snapshot

An extremely simple method for extraction of lysophospholipids and phospholipids from blood samples

inferredcites →https://doi.org/10.1194/jlr.d071068openalex-snapshot

Fluorescence-based rapid measurement of sphingosine-1-phosphate transport activity in erythrocytes

inferredcites →https://doi.org/10.1194/jlr.m085589openalex-snapshot

Contribution of the precursors and interplay of the pathways in the phospholipid metabolism of the malaria parasite

inferredcites →https://doi.org/10.12659/msm.916009openalex-snapshot

Combined Signature of the Fecal Microbiome and Plasma Metabolome in Patients with Ulcerative Colitis

inferredcites →https://doi.org/10.1371/journal.pntd.0006647openalex-snapshot

Sphingosine-1-phosphate signaling in Leishmania donovani infection in macrophages

inferredcites →https://doi.org/10.1371/journal.ppat.1006094openalex-snapshot

Stage-Specific Changes in Plasmodium Metabolism Required for Differentiation and Adaptation to Different Host and Vector Environments

inferredcites →https://doi.org/10.2119/molmed.2010.00214openalex-snapshot

S1P Is Associated with Protection in Human and Experimental Cerebral Malaria

inferredcites →https://doi.org/10.3389/fnmol.2019.00100openalex-snapshot

Stimulation of Sphingosine Kinase 1 (SPHK1) Is Beneficial in a Huntington’s Disease Pre-clinical Model

What points at this work

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

inferred← citeshttps://doi.org/10.1007/s13577-021-00513-3openalex-snapshot

Malaria link of hypertension: a hidden syndicate of angiotensin II, bradykinin and sphingosine 1-phosphate

inferred← citeshttps://doi.org/10.3389/fcimb.2020.00353openalex-snapshot

Sphingosine 1-Phosphate in Malaria Pathogenesis and Its Implication in Therapeutic Opportunities

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