Grant: Project Grant
University of Toronto
$761,176.00
Mechanisms of particle destruction and cytokine induction during phagocytosis in macrophages
EF 2018-19
Résumé
Macrophages are cells that are part of the innate immune system. These cells are specialized to perform a process called phagocytosis, whereby dying cells are engulfed and digested by the macrophage. Macrophages also clear the body of pathogens by binding specifically to them and internalizing and destroying them in an intracellular compartment. The uptake of pathogens is accelerated by opsonic receptors on macrophages that recognize antibody and complement immune mediators that specifically bind to pathogens. Here we will study how the two major opsonic receptors direct the fate of the internalized target and have evidence that complement-coated particles are physically manipulated inside the macrophage.
Interestingly, uptake of these complement targets induces proinflammatory molecules in macrophages which challenges previous findings in the field. We are cell biologists and are thus keenly interesting in elucidating the mechanisms behind these novel host cell strategies involved in innate immunity.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
401674
Name
Harrison Rene E
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Cell Biology - Molecular/Fundamental
Projecttitle
Mechanisms of particle destruction and cytokine induction during phagocytosis in macrophages
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$761,176
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Cytokines; Inflammation; Macrophages; Opsonin; Phagocytosis; Phagosome
Abstract
Macrophages are cells that are part of the innate immune system. These cells are specialized to perform a process called phagocytosis, whereby dying cells are engulfed and digested by the macrophage. Macrophages also clear the body of pathogens by binding specifically to them and internalizing and destroying them in an intracellular compartment. The uptake of pathogens is accelerated by opsonic receptors on macrophages that recognize antibody and complement immune mediators that specifically bind to pathogens. Here we will study how the two major opsonic receptors direct the fate of the internalized target and have evidence that complement-coated particles are physically manipulated inside the macrophage.
Interestingly, uptake of these complement targets induces proinflammatory molecules in macrophages which challenges previous findings in the field. We are cell biologists and are thus keenly interesting in elucidating the mechanisms behind these novel host cell strategies involved in innate immunity.
Competitiondate
201903
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Harrison, Rene E
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $761,176~ $0~