Grant: Project Grant
University of Calgary
$715,275.00
Role for Lipid Droplet Associated IL-32 in Diabetic Kidney Disease
EF 2021-22
Résumé
Diabetic kidney disease is the number one cause chronic kidney disease and end stage kidney disease. Patients with diabetic kidney disease have buildup of fat molecules called lipid droplets in their kidney. Why lipid droplets accumulate in diabetic kidney disease remains unknown. We discovered a gene called IL32 that is highly expressed in the kidneys of diabetic patients. IL32 can bind to lipid droplets when there is high sugar and signals that cause inflammation. We think that high levels of IL-32 can cause more inflammation and injury to the kidney.
We will use our kidney biobank containing over 500 patient kidney biopsies combined with cutting edge technologies to find out how lipid droplet associated IL32 can promote the progression of diabetic kidney disease. We are making "mini-kidneys" called kidney organoids from patients with diabetes that retain qualities of the patient. Using these exciting new tools, we are examining how to reduce the buildup of lipid droplets and ways to block the activity of IL32 to prevent kidney injury and disease. We believe that IL32 can also be a biomarker for predicting outcomes for diabetic kidney disease.
Programme
Project Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
452369
Name
Chun Justin
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Biomedical
Prcname2
Hematology, Digestive Disease & Kidney
Projecttitle
Role for Lipid Droplet Associated IL-32 in Diabetic Kidney Disease
Programtype2
Operating Grants
Orgnameinp2
University of Calgary
Cihramount2
$715,275
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Biomarker; Chronic Kidney Disease; Diabetes; Induced Pluripotent Stem Cells; Inflammation; Kidney Biobank; Kidney Organoids; Lipid Droplets; Spectroscopy
Abstract
Diabetic kidney disease is the number one cause chronic kidney disease and end stage kidney disease. Patients with diabetic kidney disease have buildup of fat molecules called lipid droplets in their kidney. Why lipid droplets accumulate in diabetic kidney disease remains unknown. We discovered a gene called IL32 that is highly expressed in the kidneys of diabetic patients. IL32 can bind to lipid droplets when there is high sugar and signals that cause inflammation. We think that high levels of IL-32 can cause more inflammation and injury to the kidney.
We will use our kidney biobank containing over 500 patient kidney biopsies combined with cutting edge technologies to find out how lipid droplet associated IL32 can promote the progression of diabetic kidney disease. We are making "mini-kidneys" called kidney organoids from patients with diabetes that retain qualities of the patient. Using these exciting new tools, we are examining how to reduce the buildup of lipid droplets and ways to block the activity of IL32 to prevent kidney injury and disease. We believe that IL32 can also be a biomarker for predicting outcomes for diabetic kidney disease.
Competitiondate
202109
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Chun, Justin
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $715,275~ $0~