Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.646186
Title: Interactions between platelets and platelet derived microvesicles in inflamation
Author: Box, Clare Louise
ISNI:       0000 0004 5361 0689
Awarding Body: University of Birmingham
Current Institution: University of Birmingham
Date of Award: 2015
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Abstract:
Atherosclerosis is a chronic inflammatory disease, characterised by infiltration of leukocytes and accumulation of fatty deposits in the artery wall. Early events in this disease process include recruitment of platelets to the artery wall, which in turn aid in leukocyte recruitment. However, upon activation platelets release microvesicles (PMV), we are interested in whether PMV have a role in enhancing leukocyte recruitment. We demonstrated using whole blood that upon activation, platelets form aggregates with monocytes and neutrophils. The data suggests that upon platelet activation, PMV may be generated and subsequently may have a role in heterotypic aggregate formation observed. Interestingly, lymphocytes did not form aggregates with platelets (or PMV) as readily. We showed that blocking P-selectin leads to a significant reduction in heterotypic aggregate formation. We also demonstrated the presence of P-selectin glycoprotein ligand-1 (PSGL 1), the ligand with the highest binding affinity for P-selectin, on monocytes and neutrophils. Monocytes preferentially bound platelets or PMV. However, we found no significant increase in recruitment of these heterotypic aggregates to von Willebrand factor, under conditions of low shear stress compared to monocytes alone. These heterotypic aggregates provide a mechanism for cross-talk between cell types and have a potential role in inflammatory and thrombotic diseases.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.646186  DOI: Not available
Keywords: RC Internal medicine
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