Grant: International COEN Initiative in Neurodegeneration
University of Calgary
$200,000.00
CSPG targeting for lesion regeneration in multiple sclerosis.
FY 2019-20
Summary
Primary phases of multiple sclerosis (MS) are quite well controlled by anti-inflammatory drugs. However, these early stages are invariably followed with disease longevity by an uncontrolled progressive form of the disease mostly due to the lack of pro-regeneration therapies. Chondroitin sulfate proteoglycans (CSPGs) are one family of molecules known to exert inhibition of axonal regeneration in preclinical models of brain trauma. Recently, Dr Yong's group described that CSPGS are potent inhibitors of remyelination in mouse MS models, and that aging mice showed an increased deposition of CSPGs in their lesions. Concurrently, Dr Huard's group discovered a new natural ligand for CSPGs, expressed in MS lesions, A proliferation inducing ligand (APRIL). Drs Yong and Huard have thus combined their expertise in this project to test whether CSPG inhibition by APRIL may help induce regeneration in multiple sclerosis lesions. If so, this will have a considerable impact on regenerative biology in general and MS in particular.
Department
Program
International COEN Initiative in Neurodegeneration
Recipient
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
415741
Name
Yong Voon W
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
The French National Research Agency (France)
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Special Cases
Projecttitle
CSPG targeting for lesion regeneration in multiple sclerosis.
Programtype2
Operating Grants
Orgnameinp2
University of Calgary
Cihramount2
$200,000
Cihrequipment2
$0
Programname2
International COEN Initiative in Neurodegeneration
Keyworddelim
April; Cspgs; Extracellular Matrix; Inhibitors; Models; Multiple Sclerosis; Oligodendrocyte; Regeneration; Remyelination; Scars
Abstract
Primary phases of multiple sclerosis (MS) are quite well controlled by anti-inflammatory drugs. However, these early stages are invariably followed with disease longevity by an uncontrolled progressive form of the disease mostly due to the lack of pro-regeneration therapies. Chondroitin sulfate proteoglycans (CSPGs) are one family of molecules known to exert inhibition of axonal regeneration in preclinical models of brain trauma. Recently, Dr Yong's group described that CSPGS are potent inhibitors of remyelination in mouse MS models, and that aging mice showed an increased deposition of CSPGs in their lesions. Concurrently, Dr Huard's group discovered a new natural ligand for CSPGs, expressed in MS lesions, A proliferation inducing ligand (APRIL). Drs Yong and Huard have thus combined their expertise in this project to test whether CSPG inhibition by APRIL may help induce regeneration in multiple sclerosis lesions. If so, this will have a considerable impact on regenerative biology in general and MS in particular.
Competitiondate
201911
Approvedterm2
2 yrs 0 mth
Pinamesdelim
Yong, Voon W
Approvedterm
2 ans 0 mois
Cihrcontribution2
Institute of Aging~ $200,000~ $0~