Canada Spends Logo

Explore our Budget 2026 analysis

Grant: Project Grant

University of Toronto

$803,250.00

Interaction of the Major Vault Protein with the Discoidin Domain Receptor 1 in dysregulation of matrix remodeling

FY 2021-22

Summary
In Western societies, ~45% of deaths, including certain types of invasive cancers, heart failure, and chronic kidney disease, are associated with disorganized connective tissues and loss of their normal function in a process that is called fibrosis. This widespread disorder has important implications for human health but it is not known how cells, when disrupted by disease, cause fibrosis to occur. It is also not understood how normal cell function leads to alterations of the protein structures of supporting tissues. In this proposal we have identified a new signaling system that appears to be an important contributor to the generation of fibrosis in tissues. This system is driven by the interplay between two proteins in cells in a manner that was recently discovered by us. We hope to examine how the interplay between these proteins causes fibrosis and how the interplay might be interrupted as a potential anti-fibrotic treatment.
Program
Project Grant
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
443704
Name
McCulloch Christopher A
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Musculoskeletal Health and Arthritis
Theme2
Biomedical
Prcname2
Cell Biology - Disease
Projecttitle
Interaction of the Major Vault Protein with the Discoidin Domain Receptor 1 in dysregulation of matrix remodeling
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$803,250
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Adhesion Signaling; Cell Culture; Collagen; Discoidin Domain Receptor 1; Fibrosis; Major Vault Protein; Matrix Metalloproteinases; Mice; Microscopy; Periodontitis
Abstract
In Western societies, ~45% of deaths, including certain types of invasive cancers, heart failure, and chronic kidney disease, are associated with disorganized connective tissues and loss of their normal function in a process that is called fibrosis. This widespread disorder has important implications for human health but it is not known how cells, when disrupted by disease, cause fibrosis to occur. It is also not understood how normal cell function leads to alterations of the protein structures of supporting tissues. In this proposal we have identified a new signaling system that appears to be an important contributor to the generation of fibrosis in tissues. This system is driven by the interplay between two proteins in cells in a manner that was recently discovered by us. We hope to examine how the interplay between these proteins causes fibrosis and how the interplay might be interrupted as a potential anti-fibrotic treatment.
Competitiondate
202104
Approvedterm2
5 yrs 0 mth
Pinamesdelim
McCulloch, Christopher A; Carneiro, Karina M
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $803,250~ $0~