Grant: Operating Grant
McMaster University
$536,131.00
Pathobiology of renal dysplasia: a functional role for stromally expressed beta-catenin
FY 2014-15
Summary
In Canada over 40,300 individuals in Canada underwent treatment for chronic kidney disease. The number of patients suffering from chronic kidney disease is projected to continually increase in the coming years. We recognize that chronic kidney diseases are a significant burden on patients, their families, and the healthcare system. Abnormal formation of the kidney ranks among the most common birth defects with an incidence of 1 in 250, and is a major contributing factor in childhood and adult onset kidney disease. Further, even minor alterations in kidney development are associated with adult onset hypertension (high blood pressure) and reduced kidney function. These ailments highlight the importance for understanding the processes that are required for proper kidney formation. The mission of our research program is to make significant contributions to the understanding of kidney development and associated diseases. Our research focuses on determining what role the protein, beta-catenin, is doing during normal kidney development and its relationship to kidney disease. Our proposed research uses innovative genetically modified mouse models that alter the levels of beta-catenin in specific cells of the kidney. Initial analysis of these mice demonstrates abnormalities similar to kidney maldevelopment. In Canada, these mouse models are unique to my laboratory, with only a handful in the world studying beta-catenin in renal dysplasia. We will use these mouse models to improve the understanding of beta-catenin in renal dysplasia. These preclinical studies will build the foundation to investigate new targets to be used for preventative therapeutic options aimed at reducing kidney maldevelopment to help reduce or alleviate the devastating effects of this childhood and adult kidney disease.
Department
Program
Operating Grant
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
321660
Name
Bridgewater Darren J
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Biomedical
Prcname2
Hematology, Digestive Disease & Kidney
Projecttitle
Pathobiology of renal dysplasia: a functional role for stromally expressed beta-catenin
Programtype2
Operating Grants
Orgnameinp2
McMaster University
Cihramount2
$536,131
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Beta-Catenin; Congenital Kidney Disease; Kidney; Kidney Disease; Mouse Models Of Kidney Disease
Abstract
In Canada over 40,300 individuals in Canada underwent treatment for chronic kidney disease. The number of patients suffering from chronic kidney disease is projected to continually increase in the coming years. We recognize that chronic kidney diseases are a significant burden on patients, their families, and the healthcare system. Abnormal formation of the kidney ranks among the most common birth defects with an incidence of 1 in 250, and is a major contributing factor in childhood and adult onset kidney disease. Further, even minor alterations in kidney development are associated with adult onset hypertension (high blood pressure) and reduced kidney function. These ailments highlight the importance for understanding the processes that are required for proper kidney formation. The mission of our research program is to make significant contributions to the understanding of kidney development and associated diseases. Our research focuses on determining what role the protein, beta-catenin, is doing during normal kidney development and its relationship to kidney disease. Our proposed research uses innovative genetically modified mouse models that alter the levels of beta-catenin in specific cells of the kidney. Initial analysis of these mice demonstrates abnormalities similar to kidney maldevelopment. In Canada, these mouse models are unique to my laboratory, with only a handful in the world studying beta-catenin in renal dysplasia. We will use these mouse models to improve the understanding of beta-catenin in renal dysplasia. These preclinical studies will build the foundation to investigate new targets to be used for preventative therapeutic options aimed at reducing kidney maldevelopment to help reduce or alleviate the devastating effects of this childhood and adult kidney disease.
Competitiondate
201503
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Bridgewater, Darren J
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $536,131~ $0~