Grant: Operating Grant
University of Alberta
$438,527.00
Characterization of Platelet Subpopulations based on the Heterogeneity of NOS Signaling: Significance for Hemostasis and Thrombosis
EF 2012-13
Résumé
Platelets are circulating blood particles normally responsible for stopping bleeding by forming blood clots (platelet aggregates). In conditions such as heart attack and stroke blood clots form inappropriately in sick (atherosclerotic) blood vessels. Recently, we have discovered that two types of platelets exists. One type of platelet generates the signaling molecule nitric oxide and the other type of platelet does not generate this signaling molecule. Nitric oxide is well known to inhibit platelet clot formation. Hence, we propose that platelets that do not generate nitric oxide initiate clot formation, while platelets that do generate nitric oxide limit clot formation. Hence, the purpose of our studies are 1) to investigate the biochemical and structural differences between the two platelet subtypes, 2) to investigate whether the two platelet subtypes play different roles in clot formation, and 3) to study whether patients with cardiovascular disease (specifically those having had a stroke) have altered ratios of one type of platelet to another. By the end of our studies we expect to have established
that the two platelet subtypes differ biochemically and structurally, have different roles in clot formation, and that stroke
patients have elevated levels of platelets which initiate clot formation. These basic and translational studies of platelet biology have the potential to significantly impact the health of Canadians by better predicting risk and extent of clot formation.
Programme
Operating Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
278747
Name
Jurasz Paul K
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Cardiovascular System - C: Vascular System
Projecttitle
Characterization of Platelet Subpopulations based on the Heterogeneity of NOS Signaling: Significance for Hemostasis and Thrombosis
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$438,527
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Aggregometry; Endothelial Nitric Oxide Synthase; Flow Cytometry; Fluorescence Activated Cell Sorting; Fluorescence Microscopy; Nitric Oxide; Platelet Pharmacology; Platelet Subpopulations; Quartz Crystal Microbalance Flow Assay; Stroke Patients
Abstract
Platelets are circulating blood particles normally responsible for stopping bleeding by forming blood clots (platelet aggregates). In conditions such as heart attack and stroke blood clots form inappropriately in sick (atherosclerotic) blood vessels. Recently, we have discovered that two types of platelets exists. One type of platelet generates the signaling molecule nitric oxide and the other type of platelet does not generate this signaling molecule. Nitric oxide is well known to inhibit platelet clot formation. Hence, we propose that platelets that do not generate nitric oxide initiate clot formation, while platelets that do generate nitric oxide limit clot formation. Hence, the purpose of our studies are 1) to investigate the biochemical and structural differences between the two platelet subtypes, 2) to investigate whether the two platelet subtypes play different roles in clot formation, and 3) to study whether patients with cardiovascular disease (specifically those having had a stroke) have altered ratios of one type of platelet to another. By the end of our studies we expect to have established
that the two platelet subtypes differ biochemically and structurally, have different roles in clot formation, and that stroke
patients have elevated levels of platelets which initiate clot formation. These basic and translational studies of platelet biology have the potential to significantly impact the health of Canadians by better predicting risk and extent of clot formation.
Competitiondate
201303
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Jurasz, Paul K
Approvedterm
4 ans 0 mois
Cihrcontribution2
~ $438,527~ $0~