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Grant: Operating Grant

University of British Columbia

$664,857.00

Dysregulated STAT-3 activation underlies lung fibroblast heterogeneity: Implications for idiopathic pulmonary fibrosis

FY 2008-09

Summary
Idiopathic pulmonary fibrosis (IPF) is a devastating disease since there is no cure or effective therapy. In North America and Canada there are over 200,000 patients with this disease. Of these more than 40,000 die annually. Currently we think that the pathology of IPF follows a pathway similar to normal wound healing, although there is progression of the disease because the normal "braking" mechanisms do not function properly. As a consequence, too much connective tissue is produced in the lungs and the ability to transfer oxygen to the bloodstream is severely impaired. My research focuses on the cells that produce the connective tissue, called myofibroblasts. We have identified a protein that we think regulates how myofibroblasts appear in the lung and produce connective tissue but do not die. By reducing the activation of this protein, the hope is that we can make myofibroblasts function normally.
Program
Operating Grant
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
181521
Name
Knight Darryl A
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Respiratory System
Projecttitle
Dysregulated STAT-3 activation underlies lung fibroblast heterogeneity: Implications for idiopathic pulmonary fibrosis
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$664,857
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Fibroblasts; Fibrosis; Human; Lung; Remodeling; Respiratory; Signaling; Stat-3
Abstract
Idiopathic pulmonary fibrosis (IPF) is a devastating disease since there is no cure or effective therapy. In North America and Canada there are over 200,000 patients with this disease. Of these more than 40,000 die annually. Currently we think that the pathology of IPF follows a pathway similar to normal wound healing, although there is progression of the disease because the normal "braking" mechanisms do not function properly. As a consequence, too much connective tissue is produced in the lungs and the ability to transfer oxygen to the bloodstream is severely impaired. My research focuses on the cells that produce the connective tissue, called myofibroblasts. We have identified a protein that we think regulates how myofibroblasts appear in the lung and produce connective tissue but do not die. By reducing the activation of this protein, the hope is that we can make myofibroblasts function normally.
Competitiondate
200903
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Knight, Darryl A
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $664,857~ $0~
University of British Columbia - $664,857 Grant (2008… | Canada Spends