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The role of platelet dysfunction in promoting diabetic thrombo-inflammation.

PGR-P-194

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Key facts

Type of research degree
4 year PhD
Application deadline
Ongoing deadline
Country eligibility
International (outside UK)
Funding
Non-funded
Supervisors
Professor Ramzi Ajjan and Professor Khalid Naseem
Schools
School of Medicine
Research groups/institutes
Leeds Institute of Cardiovascular and Metabolic Medicine
<h2 class="heading hide-accessible">Summary</h2>

Insulin resistance (IR), defined as resistance to insulin-stimulated glucose uptake, is a common precursor to both diabetes and associated vascular disease. IR is a multi-system disorder that is characterised by multiple metabolic and cellular alterations including atherogenic dyslipidemia, glucose intolerance and inflammation. In subjects with Type 2 diabetes (T2D) immune cells are transformed into a proinflammatory state that is associated with increased production of the cytokine interleukin 1b (IL-1b). 1 This proinflammatory cytokine is deposited in the vascular wall of atherosclerotic coronary arteries in humans and promotes several atheroclertoic processes in mice 2. These observations are the basis for a large scale clinical trial (CANTOS) targeting IL-1b with a human monoclonal antibody to reduce of the incidence of myocardial infarction.

<h2 class="heading hide-accessible">Full description</h2>

<p>Subjects with type 2 diabetes (T2D) have increased circulating levels of platelet-monocyte complexes that are known to drive vascular inflammation. 3 However, the precise role of platelet-mediated inflammation in T2D is unclear. Recent evidence suggests platelet driven inflammation proceeds through the ability to modify their proteome. Experiments performed in vitro demonstrate that platelets produce proteins that potentially influence the thromboinflammatory process including IL-1b. 4 In immune cells IL-1bis generated through the activation of inflammasomes, multimeric protein signaling complexes that trigger the activation of caspase-1 and maturation of IL-1b. The most widely characterised of these is the NOD-like receptor (NLR)P3 inflammasome and is proposed to be expressed in human platelets 5.</p> <p>In this project you will establish the molecular mechanisms that facilitate platelet IL-1b production and determine if the capacity for platelet IL-1bsynthesis is elevated in patients with T2D. The project provides excellent opportunity to gain training in a wide range of cell and molecular biology techniques, including immunoblotting, immunoprecipitation, flow cytometry, immunofluorescence, super-resolution microscopy and in vivo thrombosis assays.</p> <h3>References:</h3> <p>Lee, H.-M. et al. Upregulated NLRP3 Inflammasome Activation in Patients With Type 2 Diabetes. Diabetes 62, 194&ndash;204 (2013).</p> <p>Kaptoge, S. et al. Inflammatory cytokines and risk of coronary heart disease: new prospective study and updated meta-analysis. Eur Heart J 35, 578&ndash;589 (2014).</p> <p>Ferroni, P., Basili, S., Falco, A. &amp; Dav&igrave;, G. Platelet activation in type 2 diabetes mellitus. J Thromb Haemost 2, 1282&ndash;1291 (2004).</p> <p>Lindemann, S. et al. Activated platelets mediate inflammatory signaling by regulated interleukin 1&beta; synthesis. J Cell Biology 154, 485&ndash;490 (2001).</p> <p>Abderrazak, A. et al. NLRP3 inflammasome: From a danger signal sensor to a regulatory node of oxidative stress and inflammatory diseases. Redox Biology 4, 296&ndash;307 (2015).</p>

<h2 class="heading">How to apply</h2>

<p>Please note these are not standalone projects and applicants must apply to the PhD academy directly.</p> <p>Applications can be made at any time. You should complete an <a href="https://medicinehealth.leeds.ac.uk/faculty-graduate-school/doc/apply-2">online application form</a> and attach the following documentation to support your application.&nbsp;</p> <ul> <li>a full academic CV</li> <li>degree certificate and transcripts of marks (or marks so far if still studying)</li> <li>Evidence that you meet the programme&rsquo;s minimum English language requirements (if applicable, see requirement below)</li> <li>Evidence of funding to support your studies</li> </ul> <p>To help us identify that you are applying for this project please ensure you provide the following information on your application form;</p> <ul> <li>Select PhD in Cardiovascular and Metabolic Disease as your programme of study</li> <li>Give the full project title and name the supervisors listed in this advert</li> </ul>

<h2 class="heading heading--sm">Entry requirements</h2>

A degree in biological sciences, dentistry, medicine, midwifery, nursing, psychology or a good honours degree in a subject relevant to the research topic. A Masters degree in a relevant subject may also be required in some areas of the Faculty. For entry requirements for all other research degrees we offer, please contact us.

<h2 class="heading heading--sm">English language requirements</h2>

Applicants whose first language is not English must provide evidence that their English language is sufficient to meet the specific demands of their study. The minimum requirements for this programme in IELTS and TOEFL tests are: &bull; British Council IELTS - score of 7.0 overall, with no element less than 6.5 &bull; TOEFL iBT - overall score of 100 with the listening and reading element no less than 22, writing element no less than 23 and the speaking element no less than 24.

<h2 class="heading">Contact details</h2>

<p>For further information please contact the Faculty Graduate School<br /> e:<a href="mailto:fmhpgradmissions@leeds.ac.uk">fmhpgradmissions@leeds.ac.uk</a></p>


<h3 class="heading heading--sm">Linked research areas</h3>