Grant: Operating Grant
Université de Sherbrooke
$475,800.00
Novel mechanism of atherosclerotic plaque progression mediated by mouse Mast Cell Protease-4
FY 2013-14
Summary
Mast cells are crucially involved in the body responses to a multitude of pathogens. Recent studies demonstrate that activated mast cells are involved in the progression and subsequent detachment of atherosclerotic plaque.
We have recently shown that mast cell derived chymase generates endothelin-1 (ET-1), a pro-atherogenic peptide.
The present project will firstly identify the contribution of mast-cell dependent production of ET-1 in an established mouse model of atherosclerosis via several molecular, biochemical and whole animal approaches.
We suggest that the present project may lay novel foundations of an efficient approach to reduce atherosclerotic progression and plaque instability.
Department
Program
Operating Grant
Recipient
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
305771
Name
D'Orléans-Juste Pedro
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Cardiovascular System - A: Cells and Tissues
Projecttitle
Novel mechanism of atherosclerotic plaque progression mediated by mouse Mast Cell Protease-4
Programtype2
Operating Grants
Orgnameinp2
Université de Sherbrooke
Cihramount2
$475,800
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Angiotensin Ii; Atherosclerosis; Chymase; Endothelin-1; Knock Out Mice; Mouse Mast Cell Protease 4; Pharmacology; Triple-Tof- Lc/Ms/Ms
Abstract
Mast cells are crucially involved in the body responses to a multitude of pathogens. Recent studies demonstrate that activated mast cells are involved in the progression and subsequent detachment of atherosclerotic plaque.
We have recently shown that mast cell derived chymase generates endothelin-1 (ET-1), a pro-atherogenic peptide.
The present project will firstly identify the contribution of mast-cell dependent production of ET-1 in an established mouse model of atherosclerosis via several molecular, biochemical and whole animal approaches.
We suggest that the present project may lay novel foundations of an efficient approach to reduce atherosclerotic progression and plaque instability.
Competitiondate
201403
Approvedterm2
5 yrs 0 mth
Pinamesdelim
D'Orléans-Juste, Pedro
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $475,800~ $0~