Grant: Project Grant
Sunnybrook Research Institute (Toronto, Ontario)
$860,625.00
Transcriptional regulation of gamma delta T-cell development and functional diversification
EF 2016-17
Résumé
Gamma-delta T cells act as a first line of defense against pathogens in barrier tissues such as the gut and lung. They act to directly combat bacteria and fungi, and also send out signals to additional cells to join the immune response. However, they can also contribute to autoimmune diseases and promote cancer progression. The ability of these cells to perform these functions is set up during their development from blood stem cells. In this proposal, we will define the molecular events that lead to the acquisition of the pro-inflammatory IL-17 program in gamma-delta T cells. We will focus on the roles of HEB transcription factors, which control gene expression, and on the extracellular signals that modulate their activity. A better understanding of how these cells are programmed for function during T cell development will enable us to target and modulate these important immune functions to promote health and combat disease.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
356763
Name
Anderson Michele K
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
Transcriptional regulation of gamma delta T-cell development and functional diversification
Programtype2
Operating Grants
Orgnameinp2
Sunnybrook Research Institute (Toronto, Ontario)
Cihramount2
$860,625
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
E Proteins; Gamma-Delta T Cells; Gene Expression; Gene Regulatory Networks; Hematopoiesis; Il-17; T Cell Development; Thymus; Transcription Factors
Abstract
Gamma-delta T cells act as a first line of defense against pathogens in barrier tissues such as the gut and lung. They act to directly combat bacteria and fungi, and also send out signals to additional cells to join the immune response. However, they can also contribute to autoimmune diseases and promote cancer progression. The ability of these cells to perform these functions is set up during their development from blood stem cells. In this proposal, we will define the molecular events that lead to the acquisition of the pro-inflammatory IL-17 program in gamma-delta T cells. We will focus on the roles of HEB transcription factors, which control gene expression, and on the extracellular signals that modulate their activity. A better understanding of how these cells are programmed for function during T cell development will enable us to target and modulate these important immune functions to promote health and combat disease.
Competitiondate
201610
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Anderson, Michele K
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $860,625~ $0~