Dr Robin N. PostonHonorary Reader Centre: Microvascular Research Email: r.poston@qmul.ac.ukTelephone: +44(0) 20 7882 3892ProfileResearchPublicationsSponsorsCollaboratorsProfileRobin Poston is an academic pathologist who studied Medicine at Cambridge University and the Middlesex Hospital, London, and spent many years in the Medical School at Guy’s Hospital, (now part of King’s College London). He focused on atherosclerosis research, and made the original observations indicating that adhesion molecules attract blood leukocytes to human atherosclerotic plaques. Robert Poston is a Principal Investigator at the Centre for Microvascular Research.ResearchBinding and oxidation of LDL by the endothelium in atherosclerosisAlthough the oxidation of LDL has been classically associated with macrophages, endothelial cells are also capable, and the important function of ox-LDL is in targeting and activating endothelial cells towards atherosclerotic processes. With support from the William Harvey Research Foundation, we have new evidence of the association of ox-LDL with the endothelium, in human atherosclerosis, in cultured endothelial cells, and in the periphery in an animal model of hyperlipidaemia. We wish to find the mechanisms of this oxidation, and determine its role in atherosclerosis. A research grant application is currently being submitted to the British Heart Foundation by Dr Poston and Professor Nourshargh. CD36 inhibitors and treatment of the metabolic syndromeDr Poston is a co-founder of a biotech company, Arteria (France), which has developed as series of low molecular weight CD36 inhibitors. CD36 is a scavenger receptor implicated in atherosclerosis, and is also a lipid transporter involved in the induction of insulin resistance in Type II diabetes. In pre-clinical trials, these compounds have shown promise in the treatment of diabetes and atherosclerosis, and also have activity against heart failure. Clinical trials are currently being planned, and may be organised within the Barts and the London Hospital NHS Trust. Publications Poston RN, Chughtai J, Ujkaj D et al. (publicationYear). Monocytic Cell Adhesion to Oxidised Ligands: Relevance to Cardiovascular Disease. nameOfConference DOI: 10.3390/biomedicines10123083 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/83452 Karamanavi E, McVey DG, van der Laan SW et al. (2022). The FES Gene at the 15q26 Coronary-Artery-Disease Locus Inhibits Atherosclerosis. nameOfConference DOI: 10.1161/circresaha.122.321146 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/83640 Barkaway A, Rolas L, Joulia R et al. (2021). Age-related changes in the local milieu of inflamed tissues cause aberrant neutrophil trafficking and subsequent remote organ damage. nameOfConference DOI: 10.1016/j.immuni.2021.04.025 QMRO: https://qmro.qmul.ac.uk/xmlui/handle/123456789/72327 An W, Luong LA, Bowden NP et al. (2022). Cezanne is a critical regulator of pathological arterial remodelling by targeting β-catenin signalling. nameOfConference DOI: 10.1093/cvr/cvab056 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/70862 Karamanavi E, Mcvey DG, Van Der Laan SW et al. (2020). The FES gene, located at the chromosome 15Q21.6 coronary-artery-disease locus, modulates atherosclerotic plaque vulnerability. nameOfConference DOI: 10.1016/j.atherosclerosis.2020.10.070 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/83759 Heister PM, Poston RN (2020). Pharmacological hypothesis: TPC2 antagonist tetrandrine as a potential therapeutic agent for COVID‐19. nameOfConference DOI: 10.1002/prp2.653 QMRO: qmroHref Yang X, Yang W, McVey DG et al. (2020). FURIN Expression in Vascular Endothelial Cells Is Modulated by a Coronary Artery Disease–Associated Genetic Variant and Influences Monocyte Transendothelial Migration. nameOfConference DOI: 10.1161/jaha.119.014333 QMRO: qmroHref Read JE, Luo D, Chowdhury TT et al. (2020). Magnetically responsive layer-by-layer microcapsules can be retained in cells and under flow conditions to promote local drug release without triggering ROS production. nameOfConference DOI: 10.1039/c9nr10329e QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/64585 Arokiasamy S, King R, Boulaghrasse H et al. (2019). Heparanase-dependent Remodelling of Initial Lymphatic Glycocalyx 1 Regulates Tissue-fluid Drainage during Acute Inflammation in vivo. nameOfConference DOI: 10.3389/fimmu.2019.02316 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/60002 Poston RN (2019). Atherosclerosis: integration of its pathogenesis as a self-perpetuating propagating inflammation: a review.. nameOfConference DOI: 10.1097/xce.0000000000000172 QMRO: qmroHref Luo D, Poston RN, Gould DJ et al. (2019). Magnetically targetable microcapsules display subtle changes in permeability and drug release in response to a biologically compatible low frequency alternating magnetic field. nameOfConference DOI: 10.1016/j.msec.2018.10.031 QMRO: qmroHref Tarvala U, Poston RN (2018). P31 VARIATION OF VON-WILLEBRAND FACTOR EXPRESSION IN THE ENDOTHELIUM OF HUMAN CORONARY ATHEROSCLEROTIC PLAQUES: IMPLICATIONS FOR THROMBOSIS. nameOfConference DOI: 10.1093/cvr/cvy216.034 QMRO: qmroHref Tarvala U, Matary RE, Nightingale T et al. (2018). Decrease in Von-Willebrand factor protein in the endothelium of human coronary atherosclerotic plaques: Possible mechanisms and role in thrombosis. nameOfConference DOI: 10.1016/j.atherosclerosis.2018.06.257 QMRO: qmroHref Gai M, Kurochkin MA, Li D et al. (2018). In-situ NIR-laser mediated bioactive substance delivery to single cell for EGFP expression based on biocompatible microchamber-arrays.. nameOfConference DOI: 10.1016/j.jconrel.2018.02.044 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/39107 Tarvala U, Poston RN (2018). Variation of von-Willebrand Factor Expression in the Endothelium of Human Coronary Atherosclerotic Plaques: Implications for Thrombosis. nameOfConference DOI: doi QMRO: qmroHref Chan K, Pu X, Sandesara P et al. (2017). Genetic Variation at the ADAMTS7 Locus is Associated With Reduced Severity of Coronary Artery Disease. nameOfConference DOI: 10.1161/jaha.117.006928 QMRO: qmroHref Chan K, Patel R, Pu X et al. (2017). Genetic variation at ADAMTS7 and severity of coronary artery disease. nameOfConference DOI: 10.1016/s0140-6736(17)30427-0 QMRO: qmroHref Yang W, Ng FL, Chan K et al. (2016). Coronary-Heart-Disease-Associated Genetic Variant at the COL4A1/COL4A2 Locus Affects COL4A1/COL4A2 Expression, Vascular Cell Survival, Atherosclerotic Plaque Stability and Risk of Myocardial Infarction. nameOfConference DOI: 10.1371/journal.pgen.1006127 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/13881 Nasr H, Torsney E, Poston RN et al. (2015). Investigating the Effect of a Single Infusion of Reconstituted High-Density Lipoprotein in Patients with Symptomatic Carotid Plaques. nameOfConference DOI: 10.1016/j.avsg.2015.04.084 QMRO: qmroHref Chan K, Patel R, Pu X et al. (2015). 189 Genetic Variation in ADAMTS7 is Associated with Severity of Coronary Artery Disease. nameOfConference DOI: 10.1136/heartjnl-2015-308066.189 QMRO: qmroHref Pu X, Xiao Q, Kiechl S et al. (2013). YIA3: ADAMTS7 CLEAVAGE AND VASCULAR SMOOTH MUSCLE CELL MIGRATION IS AFFECTED BY A CORONARY ARTERY DISEASE ASSOCIATED VARIANT. nameOfConference DOI: 10.1136/heartjnl-2013-304019.270 QMRO: qmroHref Pu X, Xiao Q, Kiechl S et al. (2013). ADAMTS7 Cleavage and Vascular Smooth Muscle Cell Migration Is Affected by a Coronary-Artery-Disease-Associated Variant. nameOfConference DOI: 10.1016/j.ajhg.2013.01.012 QMRO: qmroHref Motterle A, Pu X, Wood H et al. (2012). Functional analyses of coronary artery disease associated variation on chromosome 9p21 in vascular smooth muscle cells. nameOfConference DOI: 10.1093/hmg/dds224 QMRO: qmroHref Foster PA, Costa SKP, Poston R et al. (2003). Endothelial cells play an essential role in the thermal hyperalgesia induced by nerve growth factor. nameOfConference DOI: 10.1096/fj.02-1000fje QMRO: qmroHref Sponsors William Harvey Research Foundation CollaboratorsInternal Professor Carol Shoulders (WHRI) Dr Dianne Cooper (WHRI) Dr Egle Solito (WHRI) Professor Shu Ye (WHRI) Professor Graham Hitman (Blizard Institute) External Dr David Leake (University of Reading) Back to top