Grant: Operating Grant
McGill University
$818,271.00
Nuclear signalling by GPCRs and G proteins.
EF 2011-12
Résumé
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 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 targetted to internal cellular structures such as the nucleus, ER and Golgi apparatus. In these sites, they regulate a number of cellular events in a distinct manner from those they regulate at the cell surface. We are interested in determining how these signalling systems are differentially targetted and how they may play novel roles in cellular metabolism in health and disease.
Programme
Operating Grant
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
236988
Name
Hébert Terence E
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Pharmacology & Toxicology
Projecttitle
Nuclear signalling by GPCRs and G proteins.
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$818,271
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Cardiomyocyte; Cellular Signalling; Endomembrane; G Protein-Coupled Receptors; G Proteins; Imaging; Nucleus; Signalling Complexes; Transcription; Transcription Factor
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 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 targetted to internal cellular structures such as the nucleus, ER and Golgi apparatus. In these sites, they regulate a number of cellular events in a distinct manner from those they regulate at the cell surface. We are interested in determining how these signalling systems are differentially targetted and how they may play novel roles in cellular metabolism in health and disease.
Competitiondate
201109
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Hébert, Terence E
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $818,271~ $0~