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dc.date.accessioned2020-04-29T14:04:35Z
dc.date.accessioned2020-05-11T11:34:57Z
dc.date.available2020-04-29T14:04:35Z
dc.date.available2020-05-11T11:34:57Z
dc.date.issued23/04/2015
dc.identifier.citationMagwenzi S, Woodward C, Wraith KS et al (2015) Oxidised LDL activates blood platelets through CD36/NOX2-mediated inhibition of the cGMP/protein kinase G signalling cascade. Blood. 125(17): 2693-2703.
dc.identifier.urihttp://hdl.handle.net/10454/17793
dc.descriptionNo
dc.description.abstractOxidized low-density lipoprotein (oxLDL) promotes unregulated platelet activation in dyslipidemic disorders. Although oxLDL stimulates activatory signaling, it is unclear how these events drive accelerated thrombosis. Here, we describe a mechanism for oxLDL-mediated platelet hyperactivity that requires generation of reactive oxygen species (ROS). Under arterial flow, oxLDL triggered sustained generation of platelet intracellular ROS, which was blocked by CD36 inhibitors, mimicked by CD36-specific oxidized phospholipids, and ablated in CD36(-/-) murine platelets. oxLDL-induced ROS generation was blocked by the reduced NAD phosphate oxidase 2 (NOX2) inhibitor, gp91ds-tat, and absent in NOX2(-/-) mice. The synthesis of ROS by oxLDL/CD36 required Src-family kinases and protein kinase C (PKC)-dependent phosphorylation and activation of NOX2. In functional assays, oxLDL abolished guanosine 3',5'-cyclic monophosphate (cGMP)-mediated signaling and inhibited platelet aggregation and arrest under flow. This was prevented by either pharmacologic inhibition of NOX2 in human platelets or genetic ablation of NOX2 in murine platelets. Platelets from hyperlipidemic mice were also found to have a diminished sensitivity to cGMP when tested ex vivo, a phenotype that was corrected by infusion of gp91ds-tat into the mice. This study demonstrates that oxLDL and hyperlipidemia stimulate the generation of NOX2-derived ROS through a CD36-PKC pathway and may promote platelet hyperactivity through modulation of cGMP signaling.
dc.description.sponsorshipthe British Heart Foundation (PG/11/37/28884 and PG/13/90/30578) and Heart Research UK (RG2614)
dc.language.isoen
dc.subjectBlood platelets
dc.subjectcd36 antigens
dc.subjectcurrent good manufacturing practice
dc.subjectCybb gene
dc.subjectCyclic gmp
dc.subjectlow-density lipoproteins
dc.subjectSignal transduction
dc.subjectHyperlipidemia
dc.subjectCyclic gmp-dependent protein kinases
dc.subjectMice
dc.titleOxidised LDL activates blood platelets through CD36/NOX2-mediated inhibition of the cGMP/protein kinase G signalling cascade
dc.status.refereedYes
dc.date.Accepted03/02/2015
dc.date.application20/02/2015
dc.typeArticle
dc.type.versionNo full-text in the repository
dc.identifier.doihttps://doi.org/10.1182/blood-2014-05-574491
dc.date.updated2020-04-29T13:04:36Z
dc.openaccess.statusclosedAccess


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