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Grant: Project Grant

McGill University

$979,200.00

The impact of nuclear G protein signalling in health and disease

FY 2017-18

Summary
When you think about molecules like adrenaline and how they interact with the cell- you usually think of a cell surface receptor and events controlled from that location. The classical view of cellular signalling through G protein-coupled receptors (GPCRs) is that they signal exclusively at the cell surface. However, many recent studies have demonstrated that not all of these receptors are transported to the cell surface and may in fact be targeted to internal cellular structures such as the nucleus, ER and Golgi apparatus. Further, their signalling partners known as G proteins may also either be localized or moved to these alternative destinations in response to activation. In these sites, GPCRs and G proteins regulate a number of cellular events in a distinct manner from those they regulate at the cell surface. We are interested in determining if these signalling systems can differentially targeted by drugs and how they may play novel roles in cellular metabolism in health and disease.
Program
Project Grant
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
379724
Name
Hébert Terence E
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Pharmacology & Toxicology
Projecttitle
The impact of nuclear G protein signalling in health and disease
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$979,200
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Cardiac Fibrosis; Cardiac Hypertrophy; Cellular Signalling; Developmental Disorders; G Proteins; Inducible Pluripotent Stem Cells
Abstract
When you think about molecules like adrenaline and how they interact with the cell- you usually think of a cell surface receptor and events controlled from that location. The classical view of cellular signalling through G protein-coupled receptors (GPCRs) is that they signal exclusively at the cell surface. However, many recent studies have demonstrated that not all of these receptors are transported to the cell surface and may in fact be targeted to internal cellular structures such as the nucleus, ER and Golgi apparatus. Further, their signalling partners known as G proteins may also either be localized or moved to these alternative destinations in response to activation. In these sites, GPCRs and G proteins regulate a number of cellular events in a distinct manner from those they regulate at the cell surface. We are interested in determining if these signalling systems can differentially targeted by drugs and how they may play novel roles in cellular metabolism in health and disease.
Competitiondate
201803
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Hébert, Terence E
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $979,200~ $0~
McGill University - $979,200 Grant (2017-18) | Canada Spends