Grant: Project Grant
University of Toronto
$902,700.00
Control of inflammation by a novel cytosolic Unfolded Protein Response (UPR) pathway
EF 2016-17
Résumé
Inflammation is controlled by several families of proteins that assemble in large clusters when they are activated. Because this assembly is very much like a "chain reaction" it needs to be controlled at a molecular level, otherwise these clusters would precipitate into massive aggregates that could be toxic for cells. Indeed, it is known that cells need to avoid the formation of large protein aggregates, as evidenced by the pathological accumulation of those in neurodegenerative disorders. We have identified the mechanism by which these protein complexes are regulated. This leads us to hypothesize that this process is critical for the regulation of inflammation and host defense against infection. We will test this in vitro, in mouse models and in cells from patients suffering from chronic inflammatory conditions, such as Crohn's disease or auto-inflammatory syndromes named CAPS. Our research could lead to the development of novel therapeutic strategies against infectious and inflammatory diseases
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
357366
Name
Girardin Stephen E
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
Control of inflammation by a novel cytosolic Unfolded Protein Response (UPR) pathway
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$902,700
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Auto-Inflammation; Cellular Stress; Crohn'S Disease; Inflammation; Innate Immunity; Nod-Like Receptors; Pattern Recognition Molecules
Abstract
Inflammation is controlled by several families of proteins that assemble in large clusters when they are activated. Because this assembly is very much like a "chain reaction" it needs to be controlled at a molecular level, otherwise these clusters would precipitate into massive aggregates that could be toxic for cells. Indeed, it is known that cells need to avoid the formation of large protein aggregates, as evidenced by the pathological accumulation of those in neurodegenerative disorders. We have identified the mechanism by which these protein complexes are regulated. This leads us to hypothesize that this process is critical for the regulation of inflammation and host defense against infection. We will test this in vitro, in mouse models and in cells from patients suffering from chronic inflammatory conditions, such as Crohn's disease or auto-inflammatory syndromes named CAPS. Our research could lead to the development of novel therapeutic strategies against infectious and inflammatory diseases
Competitiondate
201610
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Girardin, Stephen E
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $902,700~ $0~